swMATH17969MaRDI QIDQ29820FDOQ29820
Author name not available (Why is that?)
Official website: https://github.com/chrisamiller/readDepth
Source code repository: https://github.com/chrisamiller/readDepth
Cited In (13)
- An online copy number variant detection method for short sequencing reads
- CNV-seq
- rSW-seq
- SeqBBS
- Computational exome and genome analysis
- Modeling the next generation sequencing read count data for DNA copy number variant study
- ExomeWalker
- HitWalker
- HTQC
- Jannovar
- SNVer
- SomaticSignatures
- A statistical change-point analysis approach for modeling the ratio of next generation sequencing reads
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