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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...
में बचाया:
| मुख्य लेखकों: | , , , , , |
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| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Oxford University Press
2013
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| विषय: | |
| ऑनलाइन पहुंच: | 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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