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URL: http://www.bioconductor.org/packages/release/bioc/html/exomeCopy.html
Proper Citation: exomeCopy (RRID:SCR_001276)
Description: Software package for detection of copy number variants (CNV) from exome sequencing samples, including unpaired samples. The package implements a hidden Markov model which uses positional covariates, such as background read depth and GC-content, to simultaneously normalize and segment the samples into regions of constant copy count.
Abbreviations: exomeCopy
Synonyms: exomeCopy - Copy number variant detection from exome sequencing read depth
Resource Type: software resource
Defining Citation: PMID:23089826
Keywords: copy number variation, genetics, sequencing, exome
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The NIDDK Information Network (dkNET) serves the needs of basic and clinical investigators by providing seamless access to large pools of data and research resources relevant to the mission of The National Institute of Diabetes Digestive and Kidney Diseases (NIDDK). dkNET is hosted at University of California San Diego, and is supported by NIH NIDDK grant 2U24DK097771-09.
Email: info_at_ dknet.org
