roryk/cnvkit
Copy number variant detection from targeted DNA sequencing
Best-practice pipelines for fully automated high throughput sequencing analysis
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Copy number variant detection from targeted DNA sequencing
Set of utilities to work with UPK files
BreakSeq2: Ultrafast and accurate nucleotide-resolution analysis of structural variants
My datasets - Original data or Aggregated / cleaned / restructured existing datasets. Released here under Creative Commons B