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Leveraging reads that span multiple single nucleotide polymorphisms for haplotype inference from sequencing data
Motivation: Haplotypes, defined as the sequence of alleles on one chromosome, are crucial for many genetic analyses. As experimental determination of haplotypes is extremely expensive, haplotypes are traditionally inferred using computational approaches from genotype data, i.e. the mixture of the ge...
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| Główni autorzy: | , , , , , |
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| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
Oxford University Press
2013
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| Hasła przedmiotowe: | |
| Dostęp online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3753566/ https://ncbi.nlm.nih.gov/pubmed/23825370 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btt386 |
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