From understanding tumor heterogeneity to utilizing techniques like ChIP-seq and ATAC-seq, presenters will share valuable strategies and insights valuable for those involved in cancer genomics, single-cell analysis, biomarker discovery, and more. Whether you're an expert or just curious about the role of NGS in cancer therapy, stem cell research, or epigenomics, this webinar will equip you with practical tips to take your investigations to the next level. Register today to unlock the future of cancer genomics!
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Exploring the Frontiers of Cancer Genomics with NGS
Discover how next-generation sequencing (NGS) is reshaping cancer research in our upcoming Bench Tip Webinar. In collaboration with Biocompare, the driving force behind SEQanswers, this enlightening session will dive into groundbreaking areas like chromatin regulation, resistance mechanisms in Myelodysplastic Syndrome (MDS), and single-cell profiling in liposarcoma.
From understanding tumor heterogeneity to utilizing techniques like ChIP-seq and ATAC-seq, presenters will share valuable strategies and insights valuable for those involved in cancer genomics, single-cell analysis, biomarker discovery, and more. Whether you're an expert or just curious about the role of NGS in cancer therapy, stem cell research, or epigenomics, this webinar will equip you with practical tips to take your investigations to the next level. Register today to unlock the future of cancer genomics!
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Innovations in next-generation sequencing technologies and techniques are driving more precise and comprehensive exploration of complex biological systems. Current advancements include improved accessibility for long-read sequencing and significant progress in single-cell and 3D genomics. This article explores some of the most impactful developments in the field over the past year.
Long-Read Sequencing
Long-read sequencing has seen remarkable advancements,...12-02-2024, 01:49 PM