Cargando…
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...
| Autores principales: | , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2012
|
| Materias: | |
| 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 |