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Family-Based Haplotype Estimation and Allele Dosage Correction for Polyploids Using Short Sequence Reads
DNA sequence reads contain information about the genomic variants located on a single chromosome. By extracting and extending this information using the overlaps between the reads, the haplotypes of an individual can be obtained. Using parent-offspring relationships in a population can considerably...
Autores principales: | Motazedi, Ehsan, Maliepaard, Chris, Finkers, Richard, Visser, Richard, de Ridder, Dick |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477055/ https://www.ncbi.nlm.nih.gov/pubmed/31040862 http://dx.doi.org/10.3389/fgene.2019.00335 |
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