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Cancer Research - Research Areas - GENEWIZ
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These include commercially available hotspot cancer panels, as well as Azenta’s pan-cancer and OncoGxOne™ discovery cancer panels.</p><br> <p class="text-left"><a href="https://www.genewiz.com/Public/Services/Next-Generation-Sequencing/Targeted-Resequencing-Panels/cancer-panels" class="blue-text" style="padding: 10px; background-color: #826ec3;color:#fff;">Learn More <em class="icon-3x fa fa-angle-right"></em></a></p> </div> </div> </li> <!--target=""--> <li class='col-sm-4'> <div class='SingleIcon headline-center Component-BackGround-Defaultmargin-top-0 margin-bottom-30 padding-top-10 padding-bottom-10'> <div class="row"> <img src="/-/media/Images/Home/icons/Purple-Icons/sanger-overview-110x210_Purple.ashx?h=110&la=en&w=210&hash=6A2D1890F8DD7B9B4EA2DA7B1AC514AC39C28B05" alt="Building" width="210" height="110" /> </div> <div class="row"> <h3>Sanger Sequencing</h3> <br> </div> <div class="row"> <p style="text-align: left;">We offer a range of Sanger sequencing options available to meet the cancer researcher’s basic toolkit needs. From PCR purification to direct-colony sequencing, GENEWIZ’s fast turnaround and high-quality data will accelerate the pace of your cancer-related sequence confirmation needs.</p><br> <p class="text-left"><a href="/Public/Services/Sanger-Sequencing" class="blue-text" style="padding: 10px; background-color: #826ec3;color:#fff;">Learn More <em class="icon-3x fa fa-angle-right"></em></a></p> <br> <br> <br> </div> </div> </li> <!--target=""--> <li class='col-sm-4'> <div class='SingleIcon headline-center Component-BackGround-Defaultmargin-top-0 margin-bottom-30 padding-top-10 padding-bottom-10'> <div class="row"> <img src="/-/media/Images/Home/icons/Purple-Icons/gene-synthesis_110x210_Purple.ashx?h=110&la=en&w=210&hash=61237659C1B6D3300B1F2AB38BCEFFCBCDE7F7A3" alt="Building" width="210" height="110" /> </div> <div class="row"> <h3>Gene Synthesis</h3> </div> <div class="row"> <p style="text-align: left;">Gene Synthesis services offer cancer researchers a way to characterize the effects of genomic mutations upon the mechanisms of cellular functions. 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