hsegHMM is a software tool to analyze copy number variation (CNV). The hsegHMM algorithm uses a hidden Markov model (HMM) as the basis that includes hypersegmentation and an E-M method.
Genetics; DNA structural variation; Oncology
Choo-Wosoba H, Albert PS, Zhu B "hsegHMM: hidden Markov model-based allele-specific copy number alteration analysis accounting for hypersegmentation." BMC Bioinformatics. 2018 Nov 14;19(1):424. https://doi.org/10.1186/s12859-018-2412-y
PMID: 30428830
PMCID: PMC6236906
If you find errors, please report here.
SECTIONS
TutorialsFind thousands of Bioinformatics and Life Science software tools and databases in the newly launched
Ads