ReadDepth
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Software:29820
swMATH17969MaRDI QIDQ29820FDOQ29820
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Source code repository: https://github.com/chrisamiller/readDepth
Cited In (4)
- An online copy number variant detection method for short sequencing reads
- Computational exome and genome analysis
- 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
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