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<h4><a href="https://www.youtube.com/watch?v=KXjnSHz3Jk8">Watch the webinar to gain insights on how data mining can be applied for epigenetics applications</a></h4>
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<blockquote style="padding-bottom: 0;"><span class="label-green" style="margin-bottom: 16px; margin-left: -22px; font-size: 22px;">WHITE PAPERS</span>
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<ul data-tab="" class="tips-menu">
<li><a href="#panel1" class="tips portal button">Smokers vs non-smokers </a></li>
<li><a href="#panel2" class="tips portal button">Breast cancer</a></li>
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<h3 style="margin-top: 0;">Powerful new insights with epigenetic data mining.<br /> A study to distinguish smokers from non-smokers using just one droplet of blood</h3>
<p>Next generation sequencing in combination with sophisticated bioinformatics technologies for genomic, transcriptomic and epigeneomic analyses have enormous potential to establish new biomarkers for disease diagnostics, enabling true precision medicine. Analyses of liquid biopsies to measure thousands of different data points simultaneously in easily accessible body fluids (e.g. blood, urine, and saliva) are extremely promising for such biomarker studies.<br />(...)</p>
<a href="https://www.diagenode.com/en/pages/form-bioinfo" class="alert small button" target="_blank">Read more</a></div>
<div class="content" id="panel2">
<h3 style="margin-top: 0;">Data mining on DNA methylation data in cancer samples<br />Distinguishing normal from breast cancer tissue</h3>
<p>Breast cancer is the most commonly occurring cancer in women and the second most common cancer overall.</p>
<p>One important aspect of cancer tissues it that they differ from normal tissues in their epigenetic make up, especially in the DNA methylation pattern. In normal cells methylation assures the proper regulation of gene expression and stable gene silencing. DNA methylation is associated with histone modifications, and the interplay of these epigenetic modifications is crucial to regulate the functioning of the genome by changing chromatin architecture.<br />(...)</p>
<a href="https://www.diagenode.com/en/pages/form-bioinfo?app_note=23" class="alert small button" target="_blank">Read more</a></div>
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<p>Diagenode's new data mining service utilizes methods at the frontier of machine learning, statistics, and database systems. This enhanced service supports new discoveries that were previously not possible by analyzing patterns in large data sets to give informative new insights.</p>
<p>If you have data from patient cohorts, single cell analyses or any other heterogeneous scenarios, our service team provides enhanced support with optimal data analysis using our latest data mining capabilities. Specifically, our team applies machine learning technologies to find previously undiscovered or unobvious relationships within and across datasets. This advanced technology allows discovery of informative features from mass data, essentially “finding a needle in a haystack.”</p>
<p>Diagenode utilizes multiple algorithms to achieve advanced data mining and uses the most optimal combination of algorithms specific to your data. Our goal is to build strong classifiers that separate data into two or more classes or groups depending on associated data.</p>
<p class="extra-spaced">Different and multiple -omics data classes can be mined simultaneously. Integration with phenotypic and/or clinical data is also possible. We offer data mining services for several data classes including:</p>
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<td><strong>Transcriptomic data</strong></td>
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<p>ATAC-seq</p>
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<p>mRNA-sequencing</p>
<p>Small and long non coding RNA</p>
<p>Single-cell RNA-sequencing</p>
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<p></p>
<p><strong>Biological Interpretation</strong></p>
<p class="extra-spaced">Machine learning classifiers also mirror the underlying biological differences between classes and are used to uncover the molecular processes at work. In order to achieve this, we offer biological interpretation services and pathway mining analyses for your data.</p>
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<p></p>
<div id="paper" style="text-align: center;">
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<div class="small-12 medium-12 large-12 columns">
<blockquote style="padding-bottom: 0;"><span class="label-green" style="margin-bottom: 16px; margin-left: -22px; font-size: 22px;">WHITE PAPERS</span>
<div id="portal" class="main-portal">
<div class="portal-inner"><nav class="portal-nav" style="text-align: left;">
<ul data-tab="" class="tips-menu">
<li><a href="#panel1" class="tips portal button">Smokers vs non-smokers </a></li>
<li><a href="#panel2" class="tips portal button">Breast cancer</a></li>
</ul>
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<h3 style="margin-top: 0;">Powerful new insights with epigenetic data mining.<br /> A study to distinguish smokers from non-smokers using just one droplet of blood</h3>
<p>Next generation sequencing in combination with sophisticated bioinformatics technologies for genomic, transcriptomic and epigeneomic analyses have enormous potential to establish new biomarkers for disease diagnostics, enabling true precision medicine. Analyses of liquid biopsies to measure thousands of different data points simultaneously in easily accessible body fluids (e.g. blood, urine, and saliva) are extremely promising for such biomarker studies.<br />(...)</p>
<a href="https://www.diagenode.com/en/pages/form-bioinfo" class="alert small button" target="_blank">Read more</a></div>
<div class="content" id="panel2">
<h3 style="margin-top: 0;">Data mining on DNA methylation data in cancer samples<br />Distinguishing normal from breast cancer tissue</h3>
<p>Breast cancer is the most commonly occurring cancer in women and the second most common cancer overall.</p>
<p>One important aspect of cancer tissues it that they differ from normal tissues in their epigenetic make up, especially in the DNA methylation pattern. In normal cells methylation assures the proper regulation of gene expression and stable gene silencing. DNA methylation is associated with histone modifications, and the interplay of these epigenetic modifications is crucial to regulate the functioning of the genome by changing chromatin architecture.<br />(...)</p>
<a href="https://www.diagenode.com/en/pages/form-bioinfo?app_note=23" class="alert small button" target="_blank">Read more</a></div>
</div>
</blockquote>
</div>
</div>
<p>Diagenode's new data mining service utilizes methods at the frontier of machine learning, statistics, and database systems. This enhanced service supports new discoveries that were previously not possible by analyzing patterns in large data sets to give informative new insights.</p>
<p>If you have data from patient cohorts, single cell analyses or any other heterogeneous scenarios, our service team provides enhanced support with optimal data analysis using our latest data mining capabilities. Specifically, our team applies machine learning technologies to find previously undiscovered or unobvious relationships within and across datasets. This advanced technology allows discovery of informative features from mass data, essentially “finding a needle in a haystack.”</p>
<p>Diagenode utilizes multiple algorithms to achieve advanced data mining and uses the most optimal combination of algorithms specific to your data. Our goal is to build strong classifiers that separate data into two or more classes or groups depending on associated data.</p>
<p class="extra-spaced">Different and multiple -omics data classes can be mined simultaneously. Integration with phenotypic and/or clinical data is also possible. We offer data mining services for several data classes including:</p>
<table class="extra-spaced">
<tbody>
<tr>
<td><strong>Epigenetic data</strong></td>
<td><strong>Transcriptomic data</strong></td>
</tr>
<tr>
<td>
<p>DNA Methylation (RRBS, WGBS, EPIC arrays)</p>
<p>ChIP-sequencing</p>
<p>ATAC-seq</p>
</td>
<td>
<p>mRNA-sequencing</p>
<p>Small and long non coding RNA</p>
<p>Single-cell RNA-sequencing</p>
</td>
</tr>
</tbody>
</table>
<p></p>
<p><strong>Biological Interpretation</strong></p>
<p class="extra-spaced">Machine learning classifiers also mirror the underlying biological differences between classes and are used to uncover the molecular processes at work. In order to achieve this, we offer biological interpretation services and pathway mining analyses for your data.</p>
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<li>Initial feasibility report</li>
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<p></p>
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<h2 class="diacol">ADVANTAGES</h2>
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<h2>Check out our service offerings</h2>
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<li><i class="fa fa-arrow-circle-right"></i> <a href="https://www.diagenode.com/en/p/chromatin-data-analysis">Chromatin studies (ChIP-Seq, ATAC-Seq)</a></li>
<li><i class="fa fa-arrow-circle-right"></i> <a href="https://www.diagenode.com/en/p/methylation-data-analysis">Methylation studies (WGBS, RRBS, BSAS, EPIC, MeDIP-Seq)</a></li>
<li><i class="fa fa-arrow-circle-right"></i> <a href="https://www.diagenode.com/en/p/rna-data-analysis">RNA-Seq</a></li>
<li><i class="fa fa-arrow-circle-right"></i> <a href="https://www.diagenode.com/en/p/integrative-analysis">Integrative analysis of multiple omics data</a></li>
<li><i class="fa fa-arrow-circle-right"></i> <a href="https://www.diagenode.com/en/p/data-mining-service">Data mining with machine learning techniques</a></li>
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<p>Our Epigenomics Profiling Services assure the sample preparation expertise and quality data that you seek. We provide epigenome-wide analyses for understanding epigenetic mechanisms, epigenetics-related drug discovery, transgenerational epigenetics studies, epigenetic biomarker identification (including epigenomic cancer biomarkers), and functional epigenomics. Diagenode offers expert epigenomics services that you can trust for chromatin, DNA, and RNA analysis. </p>
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<h3><span class="green">Chromatin</span> analysis</h3>
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<p><i class="fa fa-arrow-circle-right"></i> <a href="../categories/chip-seq-service">Learn more</a></p>
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<h3><span class="darkgrey">DNA methylation</span> analysis</h3>
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<li>Infinium MethylationEPIC array </li>
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<p></p>
<p><i class="fa fa-arrow-circle-right"></i> <a href="../categories/dna-methylation-profiling-services">Learn more</a></p>
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<h3><span class="diacol"><g class="gr_ gr_44 gr-alert gr_spell gr_inline_cards gr_disable_anim_appear ContextualSpelling ins-del multiReplace" id="44" data-gr-id="44">RNA-seq</g></span> analysis</h3>
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<li>mRNA<span style="display: inline !important; float: none; background-color: #f8f8f8; color: #333333; font-family: Helvetica,Arial,sans-serif; font-size: 16px; font-style: normal; font-variant: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: left; text-decoration: none; text-indent: 0px; text-transform: none; -webkit-text-stroke-width: 0px; white-space: normal; word-spacing: 0px;"> analysis</span></li>
<li>Small non-coding RNA analysis</li>
<li><b></b>Whole transcriptome analysis<br /><br /><br /><br /><br /></li>
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<p><i class="fa fa-arrow-circle-right"></i> <a href="../categories/rna-seq-category">Learn more</a></p>
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<h2 style="text-align: center;"><a class="details radius small button" href="https://www.diagenode.com/en/documents/services-flyer">DOWNLOAD OUR FLYER</a></h2>
<h2>Why Diagenode</h2>
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<li><strong>Expertise and trust</strong>: Recognized epigenetics leader, official partner of <a href="http://www.blueprint-epigenome.eu/"><g class="gr_ gr_45 gr-alert gr_spell gr_inline_cards gr_disable_anim_appear ContextualSpelling ins-del multiReplace" id="45" data-gr-id="45">BLUEPRINT</g></a>, <a href="http://ihec-epigenomes.org/">IHEC</a> <g class="gr_ gr_46 gr-alert gr_gramm gr_inline_cards gr_disable_anim_appear Punctuation only-ins replaceWithoutSep" id="46" data-gr-id="46">and</g> <a href="https://www.faang.org/">FAANG</a></li>
<li><strong>Innovative technology</strong>: Utilization of the signature Bioruptor<sup>®</sup> sonication device for optimal chromatin and DNA shearing and the IP-Star<sup>®</sup> Automation device give reproducible and reliable optimization and results</li>
<li><strong>Quality</strong>: Multiple QC steps in all workflows and validated antibodies plus reagents deliver superior data</li>
<li><strong>Flexibility</strong>: Extensive range of sample species and sample origins</li>
<li><strong>Experience</strong> in epigenomics profiling for a wide range of applications and fields of interest</li>
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<div class="block-distri"><span class="label-green" style="margin-bottom: 16px; margin-left: -3px;">ANIMALS</span><center><img width="260" height="259" alt="services chip-seq - animals" src="https://www.diagenode.com/img/categories/services/services-animals.png" caption="false" /></center></div>
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<h2>12 years of expertise and trust in epigenetics</h2>
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<li>Dedicated <strong>in-house expert</strong> for your project</li>
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<p><br />RNA-seqは、ディープシーケンス技術をを用いて、RNAの全細胞含有量であるトランスクリプトームを検査する革新的な技術です。トランスクリプトームに関するデータを取得することで、ゲノム上の情報をその機能的なタンパク質発現と結び付けることができます。細胞の発達メカニズムと疾患に関連する修飾に優れた洞察を提供します。</p>
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<div class="small-12 medium-8 large-8 columns"><a href="https://www.diagenode.com/en/p/high-throughput-3mrna-seq-services"><img width="609" height="126" alt="3'mRNA-seq" src="http://www.diagenode.com/img/banners/banner-brb-468x60.png" /></a>
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<p>当社Diagenodeのエピゲノミクスプロファイリングサービスは、次世代シーケンシング(NGS)を使用し、完全なトランスクリプトミクスプロファイリング解析に役立ちます。 トランスクリプトミクスプロファイリング解析の究極目標を目指す経験豊富な科学者チームにより設計されたRNA-seq実験では細心の注意を払いサンプル処理し、RNAライブラリー調製、高品質のデータを提供するお手伝いをします。 お客様との緊密なコミュニケーションをとりながら、当社のバイオインフォマティクス専門家が、標準およびカスタマイズされた解析、包括的なサービスを提供します。</p>
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<li><a href="https://www.diagenode.com/jp/pages/dplex">D-Plexテクノロジーの活用</a></li>
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<h3 class="text-left"><a href="https://www.diagenode.com/jp/p/rna-seq-services">長鎖ノンコーディングRNA解析を含む全トランスクリプトーム</a></h3>
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<li>遺伝子の構造、それらのスプライシングパターンおよび他の転写後修飾の調査</li>
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<div class="panel"><center><img src="http://www.diagenode.com/img/categories/services/dna-workflow.png" alt="DNA-methylation -Diagenode" /></center>
<p>DNAメチル化およびヒストン修飾のパターンは、細胞機能を維持する上で不可欠な役割を果たします。 異常なDNAメチル化 - 過剰メチル化および低メチル化 - は、癌または他の疾患のような有害転帰をもたらし得ます。ゲノムワイドDNAメチル化分析による5-mCの定量化は、疾患の検出および予後のための情報を提供することが可能です。 DiagenodeのDNAメチル化解析サービスは、あらゆる種のゲノムDNAメチル化解析の標的となる全ゲノムDNAメチル化解析用の多数のバイサルファイトシークエンシングオプションをご提供いたします。</p>
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<h3><a href="https://www.diagenode.com/jp/p/infinium-methylation-epic-array-service">Infinium MethylationEPIC Array Service</a></h3>
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<li>CpG、非CpG、およびCHH部位のメチル化部位の定量分析</li>
<li><span><a href="https://www.diagenode.com/jp/categories/bioinformatics-service">バイオインフォマティクスツール</a></span>によるDifferentially methylated site解析</li>
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<h3><a href="https://www.diagenode.com/jp/p/infinium-mouse-methylation-array-service">Infinium Mouse Methylation Array Service</a></h3>
<ul>
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<li>単一ヌクレオチド分解能で285,000を超えるマウスCpG位置</li>
<li>一般的な実験用マウス系に適応</li>
<li><span><a href="https://www.diagenode.com/jp/categories/bioinformatics-service">バイオインフォマティクスツール</a></span>によるDifferentially methylated site解析</li>
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<h3><a href="https://www.diagenode.com/jp/p/rrbs-service">Reduced Representation Bisulfite Sequencing (RRBS) サービス</a></h3>
<ul>
<li>結果に自信のある堅牢で費用効果の高いソリューション</li>
<li>単一ヌクレオチド分解能で最大500万か所のCpG部位をカバー(ヒトサンプル)</li>
<li>全ゲノム上CpG-rich部位とプロモーターのメチレーションパターン解析</li>
<li><span><a href="https://www.diagenode.com/jp/categories/bioinformatics-service">バイオインフォマティクスツール</a></span>によるDifferentially methylated site解析</li>
<li>エピジェネティックなバイオマーカーの探索に最適</li>
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<h3><a href="https://www.diagenode.com/jp/p/wgbs-service">Whole Genome Bisulfite Sequencing (WGBS) Service</a></h3>
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<li><a href="https://www.diagenode.com/jp/categories/bioinformatics-service">バイオインフォマティックスツールによるゲノムにわたるCpG、CHGおよびCHH領域のメチル化パターン解析</a></li>
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<h3><a href="https://www.diagenode.com/jp/p/targeted-dna-methylation-service">Targeted Bisulfite Sequencing Service</a></h3>
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<li><span>Choose between two methodologies depending on the size of the region of interest: PCR enrichment or hybridization capture</span></li>
<li><span>Enhanced accuracy, sensitivity and specificity while reducing overall cost</span></li>
<li><span>Allowing deep sequencing at high coverage levels for rare variant identification</span></li>
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<h3><a href="../p/medip-seq-service">MeDIP</a></h3>
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<a href="https://www.diagenode.com/en/pages/form-bioinfo" class="alert small button" target="_blank">Read more</a></div>
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<h3 style="margin-top: 0;">Data mining on DNA methylation data in cancer samples<br />Distinguishing normal from breast cancer tissue</h3>
<p>Breast cancer is the most commonly occurring cancer in women and the second most common cancer overall.</p>
<p>One important aspect of cancer tissues it that they differ from normal tissues in their epigenetic make up, especially in the DNA methylation pattern. In normal cells methylation assures the proper regulation of gene expression and stable gene silencing. DNA methylation is associated with histone modifications, and the interplay of these epigenetic modifications is crucial to regulate the functioning of the genome by changing chromatin architecture.<br />(...)</p>
<a href="https://www.diagenode.com/en/pages/form-bioinfo?app_note=23" class="alert small button" target="_blank">Read more</a></div>
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<h2 class="diacol">ADVANTAGES</h2>
<ol>
<li>The bioinformatics team works constantly to optimize pipelines to deliver biologically meaningful results within a short turnaround time</li>
<li>Flexible and communicative team work in close collaboration with you to adapt to your analysis requirements</li>
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<li><i class="fa fa-arrow-circle-right"></i> <a href="https://www.diagenode.com/en/p/chromatin-data-analysis">Chromatin studies (ChIP-Seq, ATAC-Seq)</a></li>
<li><i class="fa fa-arrow-circle-right"></i> <a href="https://www.diagenode.com/en/p/methylation-data-analysis">Methylation studies (WGBS, RRBS, BSAS, EPIC, MeDIP-Seq)</a></li>
<li><i class="fa fa-arrow-circle-right"></i> <a href="https://www.diagenode.com/en/p/rna-data-analysis">RNA-Seq</a></li>
<li><i class="fa fa-arrow-circle-right"></i> <a href="https://www.diagenode.com/en/p/integrative-analysis">Integrative analysis of multiple omics data</a></li>
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<p>Our Epigenomics Profiling Services assure the sample preparation expertise and quality data that you seek. We provide epigenome-wide analyses for understanding epigenetic mechanisms, epigenetics-related drug discovery, transgenerational epigenetics studies, epigenetic biomarker identification (including epigenomic cancer biomarkers), and functional epigenomics. Diagenode offers expert epigenomics services that you can trust for chromatin, DNA, and RNA analysis. </p>
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<h3><span class="green">Chromatin</span> analysis</h3>
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<p><i class="fa fa-arrow-circle-right"></i> <a href="../categories/chip-seq-service">Learn more</a></p>
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<h3><span class="darkgrey">DNA methylation</span> analysis</h3>
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<li>Infinium MethylationEPIC array </li>
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<p><i class="fa fa-arrow-circle-right"></i> <a href="../categories/dna-methylation-profiling-services">Learn more</a></p>
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<li>mRNA<span style="display: inline !important; float: none; background-color: #f8f8f8; color: #333333; font-family: Helvetica,Arial,sans-serif; font-size: 16px; font-style: normal; font-variant: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: left; text-decoration: none; text-indent: 0px; text-transform: none; -webkit-text-stroke-width: 0px; white-space: normal; word-spacing: 0px;"> analysis</span></li>
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<li><b></b>Whole transcriptome analysis<br /><br /><br /><br /><br /></li>
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<p><i class="fa fa-arrow-circle-right"></i> <a href="../categories/rna-seq-category">Learn more</a></p>
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<h2 style="text-align: center;"><a class="details radius small button" href="https://www.diagenode.com/en/documents/services-flyer">DOWNLOAD OUR FLYER</a></h2>
<h2>Why Diagenode</h2>
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<li><strong>Expertise and trust</strong>: Recognized epigenetics leader, official partner of <a href="http://www.blueprint-epigenome.eu/"><g class="gr_ gr_45 gr-alert gr_spell gr_inline_cards gr_disable_anim_appear ContextualSpelling ins-del multiReplace" id="45" data-gr-id="45">BLUEPRINT</g></a>, <a href="http://ihec-epigenomes.org/">IHEC</a> <g class="gr_ gr_46 gr-alert gr_gramm gr_inline_cards gr_disable_anim_appear Punctuation only-ins replaceWithoutSep" id="46" data-gr-id="46">and</g> <a href="https://www.faang.org/">FAANG</a></li>
<li><strong>Innovative technology</strong>: Utilization of the signature Bioruptor<sup>®</sup> sonication device for optimal chromatin and DNA shearing and the IP-Star<sup>®</sup> Automation device give reproducible and reliable optimization and results</li>
<li><strong>Quality</strong>: Multiple QC steps in all workflows and validated antibodies plus reagents deliver superior data</li>
<li><strong>Flexibility</strong>: Extensive range of sample species and sample origins</li>
<li><strong>Experience</strong> in epigenomics profiling for a wide range of applications and fields of interest</li>
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<div class="block-distri"><span class="label-green" style="margin-bottom: 16px; margin-left: -3px;">ANIMALS</span><center><img width="260" height="259" alt="services chip-seq - animals" src="https://www.diagenode.com/img/categories/services/services-animals.png" caption="false" /></center></div>
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<h2>12 years of expertise and trust in epigenetics</h2>
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<div class="small-12 medium-8 large-8 columns"><a href="https://www.diagenode.com/en/p/high-throughput-3mrna-seq-services"><img width="609" height="126" alt="3'mRNA-seq" src="http://www.diagenode.com/img/banners/banner-brb-468x60.png" /></a>
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<p>当社Diagenodeのエピゲノミクスプロファイリングサービスは、次世代シーケンシング(NGS)を使用し、完全なトランスクリプトミクスプロファイリング解析に役立ちます。 トランスクリプトミクスプロファイリング解析の究極目標を目指す経験豊富な科学者チームにより設計されたRNA-seq実験では細心の注意を払いサンプル処理し、RNAライブラリー調製、高品質のデータを提供するお手伝いをします。 お客様との緊密なコミュニケーションをとりながら、当社のバイオインフォマティクス専門家が、標準およびカスタマイズされた解析、包括的なサービスを提供します。</p>
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<p>DNAメチル化およびヒストン修飾のパターンは、細胞機能を維持する上で不可欠な役割を果たします。 異常なDNAメチル化 - 過剰メチル化および低メチル化 - は、癌または他の疾患のような有害転帰をもたらし得ます。ゲノムワイドDNAメチル化分析による5-mCの定量化は、疾患の検出および予後のための情報を提供することが可能です。 DiagenodeのDNAメチル化解析サービスは、あらゆる種のゲノムDNAメチル化解析の標的となる全ゲノムDNAメチル化解析用の多数のバイサルファイトシークエンシングオプションをご提供いたします。</p>
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<p>エピゲノミクスプロファイリングサービスは、全ゲノムまたは遺伝子スケールのDNAメチル化のニーズに応じた最適なソリューションをご提案し、DNAメチル化(5-mC)およびメチル化変異体(5-hmC)研究をサポートします。DNAシーケンスのためのライブラリー調製やアレイから高品質のデータをお届けし、当社のバイオインフォマティクスの専門チームがお客様の研究内容に合わせて、カスタマイズされた解析を含む包括的なサービスを提供します。<br /><br /></p>
<h3><a href="https://www.diagenode.com/jp/p/infinium-methylation-epic-array-service">Infinium MethylationEPIC Array Service</a></h3>
<ul>
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<li>単一ヌクレオチド分解能で850,000を超えるヒトCpG位置</li>
<li>CpG、非CpG、およびCHH部位のメチル化部位の定量分析</li>
<li><span><a href="https://www.diagenode.com/jp/categories/bioinformatics-service">バイオインフォマティクスツール</a></span>によるDifferentially methylated site解析</li>
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<h3><a href="https://www.diagenode.com/jp/p/infinium-mouse-methylation-array-service">Infinium Mouse Methylation Array Service</a></h3>
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<li>単一ヌクレオチド分解能で285,000を超えるマウスCpG位置</li>
<li>一般的な実験用マウス系に適応</li>
<li><span><a href="https://www.diagenode.com/jp/categories/bioinformatics-service">バイオインフォマティクスツール</a></span>によるDifferentially methylated site解析</li>
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<h3><a href="https://www.diagenode.com/jp/p/rrbs-service">Reduced Representation Bisulfite Sequencing (RRBS) サービス</a></h3>
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<li><span><a href="https://www.diagenode.com/jp/categories/bioinformatics-service">バイオインフォマティクスツール</a></span>によるDifferentially methylated site解析</li>
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<li>全ゲノム上CpG-rich部位とプロモーターのメチレーションパターン解析</li>
<li><a href="https://www.diagenode.com/jp/categories/bioinformatics-service">バイオインフォマティックスツールによるゲノムにわたるCpG、CHGおよびCHH領域のメチル化パターン解析</a></li>
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<h3><a href="../p/medip-seq-service">MeDIP</a></h3>
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<h3 style="margin-top: 0;">Powerful new insights with epigenetic data mining.<br /> A study to distinguish smokers from non-smokers using just one droplet of blood</h3>
<p>Next generation sequencing in combination with sophisticated bioinformatics technologies for genomic, transcriptomic and epigeneomic analyses have enormous potential to establish new biomarkers for disease diagnostics, enabling true precision medicine. Analyses of liquid biopsies to measure thousands of different data points simultaneously in easily accessible body fluids (e.g. blood, urine, and saliva) are extremely promising for such biomarker studies.<br />(...)</p>
<a href="https://www.diagenode.com/en/pages/form-bioinfo" class="alert small button" target="_blank">Read more</a></div>
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<h3 style="margin-top: 0;">Data mining on DNA methylation data in cancer samples<br />Distinguishing normal from breast cancer tissue</h3>
<p>Breast cancer is the most commonly occurring cancer in women and the second most common cancer overall.</p>
<p>One important aspect of cancer tissues it that they differ from normal tissues in their epigenetic make up, especially in the DNA methylation pattern. In normal cells methylation assures the proper regulation of gene expression and stable gene silencing. DNA methylation is associated with histone modifications, and the interplay of these epigenetic modifications is crucial to regulate the functioning of the genome by changing chromatin architecture.<br />(...)</p>
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<p>Diagenode's new data mining service utilizes methods at the frontier of machine learning, statistics, and database systems. This enhanced service supports new discoveries that were previously not possible by analyzing patterns in large data sets to give informative new insights.</p>
<p>If you have data from patient cohorts, single cell analyses or any other heterogeneous scenarios, our service team provides enhanced support with optimal data analysis using our latest data mining capabilities. Specifically, our team applies machine learning technologies to find previously undiscovered or unobvious relationships within and across datasets. This advanced technology allows discovery of informative features from mass data, essentially “finding a needle in a haystack.”</p>
<p>Diagenode utilizes multiple algorithms to achieve advanced data mining and uses the most optimal combination of algorithms specific to your data. Our goal is to build strong classifiers that separate data into two or more classes or groups depending on associated data.</p>
<p class="extra-spaced">Different and multiple -omics data classes can be mined simultaneously. Integration with phenotypic and/or clinical data is also possible. We offer data mining services for several data classes including:</p>
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<p><strong>Biological Interpretation</strong></p>
<p class="extra-spaced">Machine learning classifiers also mirror the underlying biological differences between classes and are used to uncover the molecular processes at work. In order to achieve this, we offer biological interpretation services and pathway mining analyses for your data.</p>
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<h3 style="margin-top: 0;">Powerful new insights with epigenetic data mining.<br /> A study to distinguish smokers from non-smokers using just one droplet of blood</h3>
<p>Next generation sequencing in combination with sophisticated bioinformatics technologies for genomic, transcriptomic and epigeneomic analyses have enormous potential to establish new biomarkers for disease diagnostics, enabling true precision medicine. Analyses of liquid biopsies to measure thousands of different data points simultaneously in easily accessible body fluids (e.g. blood, urine, and saliva) are extremely promising for such biomarker studies.<br />(...)</p>
<a href="https://www.diagenode.com/en/pages/form-bioinfo" class="alert small button" target="_blank">Read more</a></div>
<div class="content" id="panel2">
<h3 style="margin-top: 0;">Data mining on DNA methylation data in cancer samples<br />Distinguishing normal from breast cancer tissue</h3>
<p>Breast cancer is the most commonly occurring cancer in women and the second most common cancer overall.</p>
<p>One important aspect of cancer tissues it that they differ from normal tissues in their epigenetic make up, especially in the DNA methylation pattern. In normal cells methylation assures the proper regulation of gene expression and stable gene silencing. DNA methylation is associated with histone modifications, and the interplay of these epigenetic modifications is crucial to regulate the functioning of the genome by changing chromatin architecture.<br />(...)</p>
<a href="https://www.diagenode.com/en/pages/form-bioinfo?app_note=23" class="alert small button" target="_blank">Read more</a></div>
</div>
</blockquote>
</div>
</div>
<p>Diagenode's new data mining service utilizes methods at the frontier of machine learning, statistics, and database systems. This enhanced service supports new discoveries that were previously not possible by analyzing patterns in large data sets to give informative new insights.</p>
<p>If you have data from patient cohorts, single cell analyses or any other heterogeneous scenarios, our service team provides enhanced support with optimal data analysis using our latest data mining capabilities. Specifically, our team applies machine learning technologies to find previously undiscovered or unobvious relationships within and across datasets. This advanced technology allows discovery of informative features from mass data, essentially “finding a needle in a haystack.”</p>
<p>Diagenode utilizes multiple algorithms to achieve advanced data mining and uses the most optimal combination of algorithms specific to your data. Our goal is to build strong classifiers that separate data into two or more classes or groups depending on associated data.</p>
<p class="extra-spaced">Different and multiple -omics data classes can be mined simultaneously. Integration with phenotypic and/or clinical data is also possible. We offer data mining services for several data classes including:</p>
<table class="extra-spaced">
<tbody>
<tr>
<td><strong>Epigenetic data</strong></td>
<td><strong>Transcriptomic data</strong></td>
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<tr>
<td>
<p>DNA Methylation (RRBS, WGBS, EPIC arrays)</p>
<p>ChIP-sequencing</p>
<p>ATAC-seq</p>
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<td>
<p>mRNA-sequencing</p>
<p>Small and long non coding RNA</p>
<p>Single-cell RNA-sequencing</p>
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<p></p>
<p><strong>Biological Interpretation</strong></p>
<p class="extra-spaced">Machine learning classifiers also mirror the underlying biological differences between classes and are used to uncover the molecular processes at work. In order to achieve this, we offer biological interpretation services and pathway mining analyses for your data.</p>
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<h2 class="diacol">ADVANTAGES</h2>
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<li><i class="fa fa-arrow-circle-right"></i> <a href="https://www.diagenode.com/en/p/methylation-data-analysis">Methylation studies (WGBS, RRBS, BSAS, EPIC, MeDIP-Seq)</a></li>
<li><i class="fa fa-arrow-circle-right"></i> <a href="https://www.diagenode.com/en/p/rna-data-analysis">RNA-Seq</a></li>
<li><i class="fa fa-arrow-circle-right"></i> <a href="https://www.diagenode.com/en/p/integrative-analysis">Integrative analysis of multiple omics data</a></li>
<li><i class="fa fa-arrow-circle-right"></i> <a href="https://www.diagenode.com/en/p/data-mining-service">Data mining with machine learning techniques</a></li>
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<p>Our Epigenomics Profiling Services assure the sample preparation expertise and quality data that you seek. We provide epigenome-wide analyses for understanding epigenetic mechanisms, epigenetics-related drug discovery, transgenerational epigenetics studies, epigenetic biomarker identification (including epigenomic cancer biomarkers), and functional epigenomics. Diagenode offers expert epigenomics services that you can trust for chromatin, DNA, and RNA analysis. </p>
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<h3><span class="green">Chromatin</span> analysis</h3>
<ul>
<li>ChIP-seq analysis Histone modification</li>
<li>Promoter analysis</li>
<li>Enhancer analysis</li>
<li>ChIP-seq analysis Transcription factor </li>
<li>(sc)ATAC-seq Chromatin accessibility</li>
<li>ChIP-seq Cas9 off-target</li>
<li>Customized NGS service</li>
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<p><i class="fa fa-arrow-circle-right"></i> <a href="../categories/chip-seq-service">Learn more</a></p>
</div>
</div>
<div class="small-12 medium-4 large-4 columns text-left">
<div class="panel" style="border-color: #474546;">
<h3><span class="darkgrey">DNA methylation</span> analysis</h3>
<ul>
<li>Reduced representation bisulfite sequencing (RRBS)</li>
<li>Whole genome bisulfite sequencing (WGBS)</li>
<li>Targeted methylation</li>
<li>MeDIP-seq/hMeDIP-seq</li>
<li>Infinium MethylationEPIC array </li>
</ul>
<p></p>
<p><i class="fa fa-arrow-circle-right"></i> <a href="../categories/dna-methylation-profiling-services">Learn more</a></p>
</div>
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<div class="small-12 medium-4 large-4 columns text-left">
<div class="panel" style="border-color: #b11e33;">
<h3><span class="diacol"><g class="gr_ gr_44 gr-alert gr_spell gr_inline_cards gr_disable_anim_appear ContextualSpelling ins-del multiReplace" id="44" data-gr-id="44">RNA-seq</g></span> analysis</h3>
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<li>mRNA<span style="display: inline !important; float: none; background-color: #f8f8f8; color: #333333; font-family: Helvetica,Arial,sans-serif; font-size: 16px; font-style: normal; font-variant: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: left; text-decoration: none; text-indent: 0px; text-transform: none; -webkit-text-stroke-width: 0px; white-space: normal; word-spacing: 0px;"> analysis</span></li>
<li>Small non-coding RNA analysis</li>
<li><b></b>Whole transcriptome analysis<br /><br /><br /><br /><br /></li>
</ul>
<p><i class="fa fa-arrow-circle-right"></i> <a href="../categories/rna-seq-category">Learn more</a></p>
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<h2 style="text-align: center;"><a class="details radius small button" href="https://www.diagenode.com/en/documents/services-flyer">DOWNLOAD OUR FLYER</a></h2>
<h2>Why Diagenode</h2>
<ul>
<li><strong>Expertise and trust</strong>: Recognized epigenetics leader, official partner of <a href="http://www.blueprint-epigenome.eu/"><g class="gr_ gr_45 gr-alert gr_spell gr_inline_cards gr_disable_anim_appear ContextualSpelling ins-del multiReplace" id="45" data-gr-id="45">BLUEPRINT</g></a>, <a href="http://ihec-epigenomes.org/">IHEC</a> <g class="gr_ gr_46 gr-alert gr_gramm gr_inline_cards gr_disable_anim_appear Punctuation only-ins replaceWithoutSep" id="46" data-gr-id="46">and</g> <a href="https://www.faang.org/">FAANG</a></li>
<li><strong>Innovative technology</strong>: Utilization of the signature Bioruptor<sup>®</sup> sonication device for optimal chromatin and DNA shearing and the IP-Star<sup>®</sup> Automation device give reproducible and reliable optimization and results</li>
<li><strong>Quality</strong>: Multiple QC steps in all workflows and validated antibodies plus reagents deliver superior data</li>
<li><strong>Flexibility</strong>: Extensive range of sample species and sample origins</li>
<li><strong>Experience</strong> in epigenomics profiling for a wide range of applications and fields of interest</li>
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<div class="block-distri"><span class="label-green" style="margin-bottom: 16px; margin-left: -3px;">HUMAN</span><center><img width="260" height="259" alt="services chip-seq - human" src="https://www.diagenode.com/img/categories/services/services-humans.png" caption="false" /></center></div>
</li>
<li>
<div class="block-distri"><span class="label-green" style="margin-bottom: 16px; margin-left: -3px;">ANIMALS</span><center><img width="260" height="259" alt="services chip-seq - animals" src="https://www.diagenode.com/img/categories/services/services-animals.png" caption="false" /></center></div>
</li>
<li>
<div class="block-distri"><span class="label-green" style="margin-bottom: 16px; margin-left: -3px;">PLANTS</span><center><img width="260" height="259" alt="services methylation-plant" src="https://www.diagenode.com/img/categories/services/services-plants.png" caption="false" /></center></div>
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<h2>12 years of expertise and trust in epigenetics</h2>
<ul>
<li><strong>End-to-end</strong> epigenetic service</li>
<li><strong>Collaborative</strong> and customized project design</li>
<li>Dedicated <strong>in-house expert</strong> for your project</li>
<li><strong>Integrative</strong> data analysis</li>
<li>Presentation-<strong>quality data</strong> and graphs</li>
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<p>Chromatin consists of DNA, histones and non-histone proteins. Understanding the roles of histones and transcription factors is critical in understanding the regulation of gene expression.</p>
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<div class="small-12 medium-8 large-8 columns"><center><img src="http://www.diagenode.com/img/applications/histone-marks-helice.png" alt="Histone-Antibodies-Diagenode" /></center><br href="../p/service-chip-seq" />
<h3><a href="../p/atac-seq-service">ATAC-seq: open chromatin regions</a></h3>
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<h3><a href="../p/service-chip-seq">ChIP-seq/ChIP-qPCR histone modifications</a></h3>
<p>Post-translational modification of histones is implicated in the regulation of gene expression, necessitating the study of regulatory elements and their interacting proteins like active promoter and enhancer analysis. Profile genome-wide histone modifications by ChIP-seq analysis to understand transcriptional regulation</p>
<ul>
<li><strong>Active promoter profiling</strong>: H3K4me3 enrichment</li>
<li><strong>Inactive promoter profiling</strong>: H3K27me3 enrichment</li>
<li><strong>Enhancer profiling</strong>: H3K4me1 and H3K27ac enrichment in regulatory regions</li>
<li><strong>Active gene body</strong>: H3K36me3</li>
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<p>Explore the effects of transcription factor binding through ChIP-seq analysis of a multitude of TFs including:</p>
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<li>CTCF: transcriptional repressor and insulator activity</li>
<li>p300/CBP: histone acetyltransferase</li>
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<li>Epigenetic writers, readers, erasers</li>
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<h3><a href="../p/service-chip-seq">Custom NGS services</a></h3>
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<p><br />RNA-seqは、ディープシーケンス技術をを用いて、RNAの全細胞含有量であるトランスクリプトームを検査する革新的な技術です。トランスクリプトームに関するデータを取得することで、ゲノム上の情報をその機能的なタンパク質発現と結び付けることができます。細胞の発達メカニズムと疾患に関連する修飾に優れた洞察を提供します。</p>
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<p>当社Diagenodeのエピゲノミクスプロファイリングサービスは、次世代シーケンシング(NGS)を使用し、完全なトランスクリプトミクスプロファイリング解析に役立ちます。 トランスクリプトミクスプロファイリング解析の究極目標を目指す経験豊富な科学者チームにより設計されたRNA-seq実験では細心の注意を払いサンプル処理し、RNAライブラリー調製、高品質のデータを提供するお手伝いをします。 お客様との緊密なコミュニケーションをとりながら、当社のバイオインフォマティクス専門家が、標準およびカスタマイズされた解析、包括的なサービスを提供します。</p>
<h3><a href="https://www.diagenode.com/jp/p/mrna-seq-services">mRNA解析</a></h3>
<ul class="text-left">
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<li>優れた複雑性解析と高いトランスクリプトカバレッジ</li>
<li>遺伝子発現レベルの正確な比較</li>
<li>新規転写物および選択的スプライシングイベントの検出</li>
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<h3 class="text-left"><a href="https://www.diagenode.com/jp/p/small-rna-seq-services">miRNA解析を含む小さな非コードRNA</a></h3>
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<li>遺伝子発現の転写後調節の調査</li>
<li><a href="https://www.diagenode.com/jp/pages/dplex">D-Plexテクノロジーの活用</a></li>
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<h3 class="text-left"><a href="https://www.diagenode.com/jp/p/rna-seq-services">長鎖ノンコーディングRNA解析を含む全トランスクリプトーム</a></h3>
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<li>クロマチンリモデリングおよび転写/転写後調節に関与する長鎖ノンコーディングRNAの認識</li>
<li>遺伝子の構造、それらのスプライシングパターンおよび他の転写後修飾の調査</li>
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<div class="panel"><center><img src="http://www.diagenode.com/img/categories/services/dna-workflow.png" alt="DNA-methylation -Diagenode" /></center>
<p>DNAメチル化およびヒストン修飾のパターンは、細胞機能を維持する上で不可欠な役割を果たします。 異常なDNAメチル化 - 過剰メチル化および低メチル化 - は、癌または他の疾患のような有害転帰をもたらし得ます。ゲノムワイドDNAメチル化分析による5-mCの定量化は、疾患の検出および予後のための情報を提供することが可能です。 DiagenodeのDNAメチル化解析サービスは、あらゆる種のゲノムDNAメチル化解析の標的となる全ゲノムDNAメチル化解析用の多数のバイサルファイトシークエンシングオプションをご提供いたします。</p>
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<p>エピゲノミクスプロファイリングサービスは、全ゲノムまたは遺伝子スケールのDNAメチル化のニーズに応じた最適なソリューションをご提案し、DNAメチル化(5-mC)およびメチル化変異体(5-hmC)研究をサポートします。DNAシーケンスのためのライブラリー調製やアレイから高品質のデータをお届けし、当社のバイオインフォマティクスの専門チームがお客様の研究内容に合わせて、カスタマイズされた解析を含む包括的なサービスを提供します。<br /><br /></p>
<h3><a href="https://www.diagenode.com/jp/p/infinium-methylation-epic-array-service">Infinium MethylationEPIC Array Service</a></h3>
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<li>単一ヌクレオチド分解能で850,000を超えるヒトCpG位置</li>
<li>CpG、非CpG、およびCHH部位のメチル化部位の定量分析</li>
<li><span><a href="https://www.diagenode.com/jp/categories/bioinformatics-service">バイオインフォマティクスツール</a></span>によるDifferentially methylated site解析</li>
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<h3><a href="https://www.diagenode.com/jp/p/infinium-mouse-methylation-array-service">Infinium Mouse Methylation Array Service</a></h3>
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<li>単一ヌクレオチド分解能で285,000を超えるマウスCpG位置</li>
<li>一般的な実験用マウス系に適応</li>
<li><span><a href="https://www.diagenode.com/jp/categories/bioinformatics-service">バイオインフォマティクスツール</a></span>によるDifferentially methylated site解析</li>
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<h3><a href="https://www.diagenode.com/jp/p/rrbs-service">Reduced Representation Bisulfite Sequencing (RRBS) サービス</a></h3>
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<li>結果に自信のある堅牢で費用効果の高いソリューション</li>
<li>単一ヌクレオチド分解能で最大500万か所のCpG部位をカバー(ヒトサンプル)</li>
<li>全ゲノム上CpG-rich部位とプロモーターのメチレーションパターン解析</li>
<li><span><a href="https://www.diagenode.com/jp/categories/bioinformatics-service">バイオインフォマティクスツール</a></span>によるDifferentially methylated site解析</li>
<li>エピジェネティックなバイオマーカーの探索に最適</li>
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<h3><a href="https://www.diagenode.com/jp/p/wgbs-service">Whole Genome Bisulfite Sequencing (WGBS) Service</a></h3>
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<li>全ゲノム上CpG-rich部位とプロモーターのメチレーションパターン解析</li>
<li><a href="https://www.diagenode.com/jp/categories/bioinformatics-service">バイオインフォマティックスツールによるゲノムにわたるCpG、CHGおよびCHH領域のメチル化パターン解析</a></li>
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<h3><a href="https://www.diagenode.com/jp/p/targeted-dna-methylation-service">Targeted Bisulfite Sequencing Service</a></h3>
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<li><span>Enhanced accuracy, sensitivity and specificity while reducing overall cost</span></li>
<li><span>Allowing deep sequencing at high coverage levels for rare variant identification</span></li>
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<h3><a href="../p/medip-seq-service">MeDIP</a></h3>
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<h4><a href="https://www.youtube.com/watch?v=KXjnSHz3Jk8">Watch the webinar to gain insights on how data mining can be applied for epigenetics applications</a></h4>
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<blockquote style="padding-bottom: 0;"><span class="label-green" style="margin-bottom: 16px; margin-left: -22px; font-size: 22px;">WHITE PAPERS</span>
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<ul data-tab="" class="tips-menu">
<li><a href="#panel1" class="tips portal button">Smokers vs non-smokers </a></li>
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<h3 style="margin-top: 0;">Powerful new insights with epigenetic data mining.<br /> A study to distinguish smokers from non-smokers using just one droplet of blood</h3>
<p>Next generation sequencing in combination with sophisticated bioinformatics technologies for genomic, transcriptomic and epigeneomic analyses have enormous potential to establish new biomarkers for disease diagnostics, enabling true precision medicine. Analyses of liquid biopsies to measure thousands of different data points simultaneously in easily accessible body fluids (e.g. blood, urine, and saliva) are extremely promising for such biomarker studies.<br />(...)</p>
<a href="https://www.diagenode.com/en/pages/form-bioinfo" class="alert small button" target="_blank">Read more</a></div>
<div class="content" id="panel2">
<h3 style="margin-top: 0;">Data mining on DNA methylation data in cancer samples<br />Distinguishing normal from breast cancer tissue</h3>
<p>Breast cancer is the most commonly occurring cancer in women and the second most common cancer overall.</p>
<p>One important aspect of cancer tissues it that they differ from normal tissues in their epigenetic make up, especially in the DNA methylation pattern. In normal cells methylation assures the proper regulation of gene expression and stable gene silencing. DNA methylation is associated with histone modifications, and the interplay of these epigenetic modifications is crucial to regulate the functioning of the genome by changing chromatin architecture.<br />(...)</p>
<a href="https://www.diagenode.com/en/pages/form-bioinfo?app_note=23" class="alert small button" target="_blank">Read more</a></div>
</div>
</blockquote>
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<p>Diagenode's new data mining service utilizes methods at the frontier of machine learning, statistics, and database systems. This enhanced service supports new discoveries that were previously not possible by analyzing patterns in large data sets to give informative new insights.</p>
<p>If you have data from patient cohorts, single cell analyses or any other heterogeneous scenarios, our service team provides enhanced support with optimal data analysis using our latest data mining capabilities. Specifically, our team applies machine learning technologies to find previously undiscovered or unobvious relationships within and across datasets. This advanced technology allows discovery of informative features from mass data, essentially “finding a needle in a haystack.”</p>
<p>Diagenode utilizes multiple algorithms to achieve advanced data mining and uses the most optimal combination of algorithms specific to your data. Our goal is to build strong classifiers that separate data into two or more classes or groups depending on associated data.</p>
<p class="extra-spaced">Different and multiple -omics data classes can be mined simultaneously. Integration with phenotypic and/or clinical data is also possible. We offer data mining services for several data classes including:</p>
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<tbody>
<tr>
<td><strong>Epigenetic data</strong></td>
<td><strong>Transcriptomic data</strong></td>
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<p>DNA Methylation (RRBS, WGBS, EPIC arrays)</p>
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<p>ATAC-seq</p>
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<p>mRNA-sequencing</p>
<p>Small and long non coding RNA</p>
<p>Single-cell RNA-sequencing</p>
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<p></p>
<p><strong>Biological Interpretation</strong></p>
<p class="extra-spaced">Machine learning classifiers also mirror the underlying biological differences between classes and are used to uncover the molecular processes at work. In order to achieve this, we offer biological interpretation services and pathway mining analyses for your data.</p>
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<p></p>
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<h4><a href="https://www.youtube.com/watch?v=KXjnSHz3Jk8">Watch the webinar to gain insights on how data mining can be applied for epigenetics applications</a></h4>
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<blockquote style="padding-bottom: 0;"><span class="label-green" style="margin-bottom: 16px; margin-left: -22px; font-size: 22px;">WHITE PAPERS</span>
<div id="portal" class="main-portal">
<div class="portal-inner"><nav class="portal-nav" style="text-align: left;">
<ul data-tab="" class="tips-menu">
<li><a href="#panel1" class="tips portal button">Smokers vs non-smokers </a></li>
<li><a href="#panel2" class="tips portal button">Breast cancer</a></li>
</ul>
</nav></div>
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<h3 style="margin-top: 0;">Powerful new insights with epigenetic data mining.<br /> A study to distinguish smokers from non-smokers using just one droplet of blood</h3>
<p>Next generation sequencing in combination with sophisticated bioinformatics technologies for genomic, transcriptomic and epigeneomic analyses have enormous potential to establish new biomarkers for disease diagnostics, enabling true precision medicine. Analyses of liquid biopsies to measure thousands of different data points simultaneously in easily accessible body fluids (e.g. blood, urine, and saliva) are extremely promising for such biomarker studies.<br />(...)</p>
<a href="https://www.diagenode.com/en/pages/form-bioinfo" class="alert small button" target="_blank">Read more</a></div>
<div class="content" id="panel2">
<h3 style="margin-top: 0;">Data mining on DNA methylation data in cancer samples<br />Distinguishing normal from breast cancer tissue</h3>
<p>Breast cancer is the most commonly occurring cancer in women and the second most common cancer overall.</p>
<p>One important aspect of cancer tissues it that they differ from normal tissues in their epigenetic make up, especially in the DNA methylation pattern. In normal cells methylation assures the proper regulation of gene expression and stable gene silencing. DNA methylation is associated with histone modifications, and the interplay of these epigenetic modifications is crucial to regulate the functioning of the genome by changing chromatin architecture.<br />(...)</p>
<a href="https://www.diagenode.com/en/pages/form-bioinfo?app_note=23" class="alert small button" target="_blank">Read more</a></div>
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<p>Diagenode's new data mining service utilizes methods at the frontier of machine learning, statistics, and database systems. This enhanced service supports new discoveries that were previously not possible by analyzing patterns in large data sets to give informative new insights.</p>
<p>If you have data from patient cohorts, single cell analyses or any other heterogeneous scenarios, our service team provides enhanced support with optimal data analysis using our latest data mining capabilities. Specifically, our team applies machine learning technologies to find previously undiscovered or unobvious relationships within and across datasets. This advanced technology allows discovery of informative features from mass data, essentially “finding a needle in a haystack.”</p>
<p>Diagenode utilizes multiple algorithms to achieve advanced data mining and uses the most optimal combination of algorithms specific to your data. Our goal is to build strong classifiers that separate data into two or more classes or groups depending on associated data.</p>
<p class="extra-spaced">Different and multiple -omics data classes can be mined simultaneously. Integration with phenotypic and/or clinical data is also possible. We offer data mining services for several data classes including:</p>
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<td><strong>Epigenetic data</strong></td>
<td><strong>Transcriptomic data</strong></td>
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<p>ChIP-sequencing</p>
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<p>mRNA-sequencing</p>
<p>Small and long non coding RNA</p>
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<p></p>
<p><strong>Biological Interpretation</strong></p>
<p class="extra-spaced">Machine learning classifiers also mirror the underlying biological differences between classes and are used to uncover the molecular processes at work. In order to achieve this, we offer biological interpretation services and pathway mining analyses for your data.</p>
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<p><a href="https://www.diagenode.com/en/categories/Services">Read about our wetlab services</a></p>
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<h2 class="diacol">ADVANTAGES</h2>
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<li><i class="fa fa-arrow-circle-right"></i> <a href="https://www.diagenode.com/en/p/chromatin-data-analysis">Chromatin studies (ChIP-Seq, ATAC-Seq)</a></li>
<li><i class="fa fa-arrow-circle-right"></i> <a href="https://www.diagenode.com/en/p/methylation-data-analysis">Methylation studies (WGBS, RRBS, BSAS, EPIC, MeDIP-Seq)</a></li>
<li><i class="fa fa-arrow-circle-right"></i> <a href="https://www.diagenode.com/en/p/rna-data-analysis">RNA-Seq</a></li>
<li><i class="fa fa-arrow-circle-right"></i> <a href="https://www.diagenode.com/en/p/integrative-analysis">Integrative analysis of multiple omics data</a></li>
<li><i class="fa fa-arrow-circle-right"></i> <a href="https://www.diagenode.com/en/p/data-mining-service">Data mining with machine learning techniques</a></li>
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<p>Our Epigenomics Profiling Services assure the sample preparation expertise and quality data that you seek. We provide epigenome-wide analyses for understanding epigenetic mechanisms, epigenetics-related drug discovery, transgenerational epigenetics studies, epigenetic biomarker identification (including epigenomic cancer biomarkers), and functional epigenomics. Diagenode offers expert epigenomics services that you can trust for chromatin, DNA, and RNA analysis. </p>
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<div class="small-12 medium-2 large-2 columns text-left"><img src="https://www.diagenode.com/img/logo-scientist-registered-supplier.png" /></div>
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<h3><span class="green">Chromatin</span> analysis</h3>
<ul>
<li>ChIP-seq analysis Histone modification</li>
<li>Promoter analysis</li>
<li>Enhancer analysis</li>
<li>ChIP-seq analysis Transcription factor </li>
<li>(sc)ATAC-seq Chromatin accessibility</li>
<li>ChIP-seq Cas9 off-target</li>
<li>Customized NGS service</li>
</ul>
<p><i class="fa fa-arrow-circle-right"></i> <a href="../categories/chip-seq-service">Learn more</a></p>
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<h3><span class="darkgrey">DNA methylation</span> analysis</h3>
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<li>Whole genome bisulfite sequencing (WGBS)</li>
<li>Targeted methylation</li>
<li>MeDIP-seq/hMeDIP-seq</li>
<li>Infinium MethylationEPIC array </li>
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<p></p>
<p><i class="fa fa-arrow-circle-right"></i> <a href="../categories/dna-methylation-profiling-services">Learn more</a></p>
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<h3><span class="diacol"><g class="gr_ gr_44 gr-alert gr_spell gr_inline_cards gr_disable_anim_appear ContextualSpelling ins-del multiReplace" id="44" data-gr-id="44">RNA-seq</g></span> analysis</h3>
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<li>mRNA<span style="display: inline !important; float: none; background-color: #f8f8f8; color: #333333; font-family: Helvetica,Arial,sans-serif; font-size: 16px; font-style: normal; font-variant: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: left; text-decoration: none; text-indent: 0px; text-transform: none; -webkit-text-stroke-width: 0px; white-space: normal; word-spacing: 0px;"> analysis</span></li>
<li>Small non-coding RNA analysis</li>
<li><b></b>Whole transcriptome analysis<br /><br /><br /><br /><br /></li>
</ul>
<p><i class="fa fa-arrow-circle-right"></i> <a href="../categories/rna-seq-category">Learn more</a></p>
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<h2 style="text-align: center;"><a class="details radius small button" href="https://www.diagenode.com/en/documents/services-flyer">DOWNLOAD OUR FLYER</a></h2>
<h2>Why Diagenode</h2>
<ul>
<li><strong>Expertise and trust</strong>: Recognized epigenetics leader, official partner of <a href="http://www.blueprint-epigenome.eu/"><g class="gr_ gr_45 gr-alert gr_spell gr_inline_cards gr_disable_anim_appear ContextualSpelling ins-del multiReplace" id="45" data-gr-id="45">BLUEPRINT</g></a>, <a href="http://ihec-epigenomes.org/">IHEC</a> <g class="gr_ gr_46 gr-alert gr_gramm gr_inline_cards gr_disable_anim_appear Punctuation only-ins replaceWithoutSep" id="46" data-gr-id="46">and</g> <a href="https://www.faang.org/">FAANG</a></li>
<li><strong>Innovative technology</strong>: Utilization of the signature Bioruptor<sup>®</sup> sonication device for optimal chromatin and DNA shearing and the IP-Star<sup>®</sup> Automation device give reproducible and reliable optimization and results</li>
<li><strong>Quality</strong>: Multiple QC steps in all workflows and validated antibodies plus reagents deliver superior data</li>
<li><strong>Flexibility</strong>: Extensive range of sample species and sample origins</li>
<li><strong>Experience</strong> in epigenomics profiling for a wide range of applications and fields of interest</li>
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<div class="block-distri"><span class="label-green" style="margin-bottom: 16px; margin-left: -3px;">HUMAN</span><center><img width="260" height="259" alt="services chip-seq - human" src="https://www.diagenode.com/img/categories/services/services-humans.png" caption="false" /></center></div>
</li>
<li>
<div class="block-distri"><span class="label-green" style="margin-bottom: 16px; margin-left: -3px;">ANIMALS</span><center><img width="260" height="259" alt="services chip-seq - animals" src="https://www.diagenode.com/img/categories/services/services-animals.png" caption="false" /></center></div>
</li>
<li>
<div class="block-distri"><span class="label-green" style="margin-bottom: 16px; margin-left: -3px;">PLANTS</span><center><img width="260" height="259" alt="services methylation-plant" src="https://www.diagenode.com/img/categories/services/services-plants.png" caption="false" /></center></div>
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<h2>12 years of expertise and trust in epigenetics</h2>
<ul>
<li><strong>End-to-end</strong> epigenetic service</li>
<li><strong>Collaborative</strong> and customized project design</li>
<li>Dedicated <strong>in-house expert</strong> for your project</li>
<li><strong>Integrative</strong> data analysis</li>
<li>Presentation-<strong>quality data</strong> and graphs</li>
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<p>Chromatin consists of DNA, histones and non-histone proteins. Understanding the roles of histones and transcription factors is critical in understanding the regulation of gene expression.</p>
<p>Using ChIP-seq analysis, it is possible to profile histone modifications and transcription factor binding genome-wide to elucidate control of gene expression in disease or in response to a drug treatment. Diagenode’s Epigenomic Profiling Services offer a wide variety of chromatin analysis options through ChIP-seq and ATAC-seq.</p>
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<h3><a href="../p/atac-seq-service">ATAC-seq: open chromatin regions</a></h3>
<p>Study genome-wide chromatin accessibility. Identify open chromatin sites and active regulatory elements such as promoter, enhancers, and insulators.</p>
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<li><strong>Inactive promoter profiling</strong>: H3K27me3 enrichment</li>
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<p><br />RNA-seqは、ディープシーケンス技術をを用いて、RNAの全細胞含有量であるトランスクリプトームを検査する革新的な技術です。トランスクリプトームに関するデータを取得することで、ゲノム上の情報をその機能的なタンパク質発現と結び付けることができます。細胞の発達メカニズムと疾患に関連する修飾に優れた洞察を提供します。</p>
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<h3><a href="https://www.diagenode.com/jp/p/infinium-mouse-methylation-array-service">Infinium Mouse Methylation Array Service</a></h3>
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<h3><a href="https://www.diagenode.com/jp/p/rrbs-service">Reduced Representation Bisulfite Sequencing (RRBS) サービス</a></h3>
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<li><span><a href="https://www.diagenode.com/jp/categories/bioinformatics-service">バイオインフォマティクスツール</a></span>によるDifferentially methylated site解析</li>
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<h3><a href="https://www.diagenode.com/jp/p/wgbs-service">Whole Genome Bisulfite Sequencing (WGBS) Service</a></h3>
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<li><a href="https://www.diagenode.com/jp/categories/bioinformatics-service">バイオインフォマティックスツールによるゲノムにわたるCpG、CHGおよびCHH領域のメチル化パターン解析</a></li>
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<h3><a href="https://www.diagenode.com/jp/p/targeted-dna-methylation-service">Targeted Bisulfite Sequencing Service</a></h3>
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<li><span>Enhanced accuracy, sensitivity and specificity while reducing overall cost</span></li>
<li><span>Allowing deep sequencing at high coverage levels for rare variant identification</span></li>
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<h3><a href="../p/medip-seq-service">MeDIP</a></h3>
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