Genovar: a detection and visualization tool for genomic variants

BACKGROUND: Along with single nucleotide polymorphisms (SNPs), copy number variation (CNV) is considered an important source of genetic variation associated with disease susceptibility. Despite the importance of CNV, the tools currently available for its analysis often produce false positive results...

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Detalles Bibliográficos
Autores principales: Jung, Kwang Su, Moon, Sanghoon, Kim, Young Jin, Kim, Bong-Jo, Park, Kiejung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Proceedings
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3348018/
https://www.ncbi.nlm.nih.gov/pubmed/22594998
http://dx.doi.org/10.1186/1471-2105-13-S7-S12

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3348018/
https://www.ncbi.nlm.nih.gov/pubmed/22594998
http://dx.doi.org/10.1186/1471-2105-13-S7-S12

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