Cargando…
HaploShare: identification of extended haplotypes shared by cases and evaluation against controls
Recent founder mutations may play important roles in complex diseases and Mendelian disorders. Detecting shared haplotypes that are identical by descent (IBD) could facilitate discovery of these mutations. Several programs address this, but are usually limited to detecting pair-wise shared haplotype...
| Autores principales: | , , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2015
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4432975/ https://www.ncbi.nlm.nih.gov/pubmed/25956955 http://dx.doi.org/10.1186/s13059-015-0662-9 |