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Get an integrated analysis of copy number and sequence variation using data from The Cancer Genome Atlas (TCGA), and learn how CNV, allelic events, and seq. variations can aid in the discovery process in cancer studies.
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This video covers CNV calling algorithms. Common approaches, HMM (Hidden Markov Model), CBS (circular binary segmentation), and Rank Segmentation are covered along with a discussion of the pros and cons of each algorithm.
Want to learn more?
View our webinar recording on integrated analysis of sequence variations and copy number in TCGA data with Nexus Copy Number.
