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Imputing Genotypes in Biallelic Populations from Low-Coverage Sequence Data
Low-coverage next-generation sequencing methodologies are routinely employed to genotype large populations. Missing data in these populations manifest both as missing markers and markers with incomplete allele recovery. False homozygous calls at heterozygous sites resulting from incomplete allele re...
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| Publicat a: | Genetics |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Genetics Society of America
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4788230/ https://ncbi.nlm.nih.gov/pubmed/26715670 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/genetics.115.182071 |
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