Chapter 19 of 304 min read
17. CNV Calling: CNVkit, Control-FREEC, ExomeDepth, XHMM
17.1 What CNVs Are and the Core Detection Principle Copy Number Variants are large genomic segments present in an abnormal number of copies relative to the expected diploid state (2 copies) — a single copy loss…
Sign in to read this
“17. CNV Calling: CNVkit, Control-FREEC, ExomeDepth, XHMM” is for subscribers. Start with a free account — it takes a name and an email — then subscribe for $1 a month to open it.
- Python and R courses free in full