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An evaluation of copy number variation detection tools for cancer using whole exome sequencing data
BACKGROUND: Recently copy number variation (CNV) has gained considerable interest as a type of genomic/genetic variation that plays an important role in disease susceptibility. Advances in sequencing technology have created an opportunity for detecting CNVs more accurately. Recently whole exome sequ...
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| Publicado en: | BMC Bioinformatics |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BioMed Central
2017
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5452530/ https://ncbi.nlm.nih.gov/pubmed/28569140 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-017-1705-x |
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