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Comprehensive evaluation of structural variation detection algorithms for whole genome sequencing
BACKGROUND: Structural variations (SVs) or copy number variations (CNVs) greatly impact the functions of the genes encoded in the genome and are responsible for diverse human diseases. Although a number of existing SV detection algorithms can detect many types of SVs using whole genome sequencing (W...
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| Publicado no: | Genome Biol |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6547561/ https://ncbi.nlm.nih.gov/pubmed/31159850 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13059-019-1720-5 |
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