ReadDepth

MaRDI QIDQ29820swMATHFDO

Official website https://github.com/chrisamiller/readDepth

Source code repository https://github.com/chrisamiller/readDepth

Cited in

(13)

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

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