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NGScopy

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NGScopy: Detection of Copy Number Variations in Next Generation Sequencing sequencing

v1.18.0 · GPL (>=2)
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Release Lineage

Entered 3.0 · Oct 14, 2014

Removed after 3.9 · May 3, 2019

1.0 In 10 of 49 releases 3.23

Description

NGScopy provides a quantitative caller for detecting copy number variations in next generation sequencing (NGS), including whole genome sequencing (WGS), whole exome sequencing (WES) and targeted panel sequencing (TPS). The caller can be parallelized by chromosomes to use multiple processors/cores on one computer.

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Topics

Software › ResearchField › ImmunoOncology
Software › AssayDomain › CopyNumberVariation
Software › Technology › Sequencing › DNASeq
Software › Technology › Sequencing › TargetedResequencing
Software › Technology › Sequencing › ExomeSeq
Software › Technology › Sequencing › WholeGenome
Software › Technology › Sequencing

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