Cited in
(13)- Modeling the next generation sequencing read count data for DNA copy number variant study
- A statistical change-point analysis approach for modeling the ratio of next generation sequencing reads
- CNV-seq
- rSW-seq
- SeqBBS
- ExomeWalker
- HitWalker
- HTQC
- Jannovar
- SNVer
- SomaticSignatures
- Computational exome and genome analysis
- An online copy number variant detection method for short sequencing reads
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