06/17/2026
VCF (Variant Call Format) files are a cornerstone of cancer genomics, capturing genetic variants such as SNPs, insertions, deletions, and somatic mutations identified through sequencing data. By comparing tumor and normal samples, researchers can pinpoint cancer-driving mutations and uncover the molecular basis of disease.
These insights help identify actionable biomarkers, predict treatment response, study tumor evolution, and support precision oncology strategies. From mutation discovery to clinical decision-making, VCF files transform raw sequencing data into meaningful biological and therapeutic insights.
How close are we to unlocking the full potential of precision oncology?
๐ Found this helpful? ๐จ Join our ๐๐๐ง๐๐๐ซ ๐๐๐ง๐จ๐ฆ๐ข๐๐ฌ ๐๐จ๐ซ๐ค๐ฌ๐ก๐จ๐ฉ (๐๐ฎ๐ญ๐๐ญ๐ข๐จ๐ง๐๐ฅ ๐๐ง๐๐ฅ๐ฒ๐ฌ๐ข๐ฌ; ๐๐๐ซ๐ข๐๐ง๐ญ ๐๐ง๐ง๐จ๐ญ๐๐ญ๐ข๐จ๐ง, & ๐๐ฅ๐ข๐ง๐ข๐๐๐ฅ ๐๐๐ญ๐ ๐๐ง๐ญ๐๐ซ๐ฉ๐ซ๐๐ญ๐๐ญ๐ข๐จ๐ง)!
๐งฌ๐ฌ This hands-on workshop will take you through the hallmarks of cancer, key pathways, and genomic alterations, diving into driver vs. passenger mutations, SNVs, Indels, CNVs, and SVs. Explore oncogenes, tumor suppressors, and NGS data formats (FASTQ, BAM, VCF) while working with real datasets from COSMIC, TCGA, and cBioPortal.
Learn variant analysis (IGV, ANNOVAR, VEP) & clinical annotation (MAFtools, oncoplots, mutation burden analysis), and apply your skills on real cancer data. ๐
๐ For more information on workshop structure, curriculum, and training resources, register here: https://forms.gle/3GPoVrHxFpGvBt6HA
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๐๐๐ญ๐: July 6, 2026 - July 9,2026
๐ ๐๐ข๐ฆ๐: 7:00 PM IST | 8:30 AM CDT
๐ ๐๐จ๐๐๐ญ๐ข๐จ๐ง: Online