swMATH17971MaRDI QIDQ29822FDOQ29822
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Official website: http://bmcbioinformatics.biomedcentral.com/articles/10.1186/1471-2105-11-432
Cited In (6)
- MGP-HMM: detecting genome-wide CNVs using an HMM for modeling mate pair insertion sizes and read counts
- CNV-seq
- ReadDepth
- SeqBBS
- A statistical change-point analysis approach for modeling the ratio of next generation sequencing reads
- Beta approximation of ratio distribution and its application to next generation sequencing read counts
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