Changes

CNVkit

8 bytes removed, 10:43, 11 January 2016

m

Text replace - "Somatic variant calling" to "Variant calling"

|sw summary=CNVkit is a software toolkit to infer and visualize copy number from targeted DNA sequencing data.

|bio domain=Copy number estimation, Structural variation,

|bio method=Variant calling, ~~Somatic variant~~ Variant calling,

|bio tech=Illumina,

|created by=Talevich E

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