Recombination mapping using Boolean logic and high-density SNP genotyping for exome sequence filtering

Whole genome sequence data for small pedigrees has been shown to provide sufficient information to resolve detailed haplotypes in small pedigrees. Using such information, recombinations can be mapped onto chromosomes, compared with the segregation of a disease of interest and used to filter genome s...

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Bibliografiska uppgifter
Huvudupphovsmän: Markello, Thomas C., Han, Ted, Carlson-Donohoe, Hannah, Ahaghotu, Chidi, Harper, Ursula, Jones, MaryPat, Chandrasekharappa, Settara, Anikster, Yair, Adams, David R., Gahl, William A., Boerkoel, Cornelius F.
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2011
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3515651/
https://ncbi.nlm.nih.gov/pubmed/22264778
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2011.12.014
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