Literature DB >> 12603050

Selection of minimum subsets of single nucleotide polymorphisms to capture haplotype block diversity.

Hadar I Avi-Itzhak1, Xiaoping Su, Francisco M De La Vega.   

Abstract

We present a simple numerical algorithm to select the minimal subset of SNPs required to capture the diversity of haplotype blocks or other genetic loci. This algorithm can be used to quickly select the minimum SNP subset with no loss of haplotype information. In addition, the method can be used in a more aggressive mode to further reduce the original SNP set, with minimal loss of information. We demonstrate the algorithm performance with data from over 11,000 SNPs with average spacing of 6 to 11 Kb, across all the genes of chromosomes 6, 21, and 22, genotyped on DNA samples of 45 unrelated African-Americans and 45 Caucasians from the Coriell Human Diversity Collection. With no loss of information, we reduced the number of SNPs required to capture the haplotype block diversity by 25% for the African-American and 36% for the Caucasian populations. With a maximum loss of 10% of haplotype distribution information, the SNP reduction was 38% and 49% respectively for the two populations. All computations were performed in less than 1 minute for the entire dataset used.

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Year:  2003        PMID: 12603050     DOI: 10.1142/9789812776303_0044

Source DB:  PubMed          Journal:  Pac Symp Biocomput        ISSN: 2335-6928


  8 in total

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3.  Finding haplotype tagging SNPs by use of principal components analysis.

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4.  Efficient genome-wide TagSNP selection across populations via the linkage disequilibrium criterion.

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5.  Single nucleotide polymorphisms in bone turnover-related genes in Koreans: ethnic differences in linkage disequilibrium and haplotype.

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6.  FastTagger: an efficient algorithm for genome-wide tag SNP selection using multi-marker linkage disequilibrium.

Authors:  Guimei Liu; Yue Wang; Limsoon Wong
Journal:  BMC Bioinformatics       Date:  2010-01-29       Impact factor: 3.169

7.  Discovering Genome-Wide Tag SNPs Based on the Mutual Information of the Variants.

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Journal:  PLoS One       Date:  2016-12-16       Impact factor: 3.240

8.  "PolyMin": software for identification of the minimum number of polymorphisms required for haplotype and genotype differentiation.

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  8 in total

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