swMATH17970MaRDI QIDQ29821FDOQ29821
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Official website: http://bmcbioinformatics.biomedcentral.com/articles/10.1186/1471-2105-10-80
Cited In (17)
- An online copy number variant detection method for short sequencing reads
- MGP-HMM: detecting genome-wide CNVs using an HMM for modeling mate pair insertion sizes and read counts
- Change-point model on nonhomogeneous Poisson processes with application in copy number profiling by next-generation DNA sequencing
- Modeling read counts for CNV detection in exome sequencing data
- BioHMM
- seqCBS
- ReadDepth
- rSW-seq
- SeqBBS
- PICNIC
- CARAT
- ExomeCNV
- A penalized regression approach for DNA copy number study using the sequencing data
- 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
- Beta approximation of ratio distribution and its application to next generation sequencing read counts
- Modeling the evolution space of breakage fusion bridge cycles with a stochastic folding process
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