ReadDepth

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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