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SLMSuite: a suite of algorithms for segmenting genomic profiles
BACKGROUND: The identification of copy number variants (CNVs) is essential to study human genetic variation and to understand the genetic basis of mendelian disorders and cancers. At present, genome-wide detection of CNVs can be achieved using microarray or second generation sequencing (SGS) data. A...
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| Publicado no: | BMC Bioinformatics |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5490196/ https://ncbi.nlm.nih.gov/pubmed/28659129 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-017-1734-5 |
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