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A computational method for genotype calling in family-based sequencing data
BACKGROUND: As sequencing technologies can help researchers detect common and rare variants across the human genome in many individuals, it is known that jointly calling genotypes across multiple individuals based on linkage disequilibrium (LD) can facilitate the analysis of low to modest coverage s...
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| Publicado no: | BMC Bioinformatics |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4715317/ https://ncbi.nlm.nih.gov/pubmed/26772743 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-016-0880-5 |
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