Genomic Scans of Zygotic Disequilibrium and Epistatic SNPs in HapMap Phase III Populations.

Previous theory indicates that zygotic linkage disequilibrium (LD) is more informative than gametic or composite digenic LD in revealing natural population history. Further, the difference between the composite digenic and maximum zygotic LDs can be used to detect epistatic selection for fitness. He...

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Main Authors: Xin-Sheng Hu, Yang Hu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0131039
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author Xin-Sheng Hu
Yang Hu
author_facet Xin-Sheng Hu
Yang Hu
author_sort Xin-Sheng Hu
collection DOAJ
description Previous theory indicates that zygotic linkage disequilibrium (LD) is more informative than gametic or composite digenic LD in revealing natural population history. Further, the difference between the composite digenic and maximum zygotic LDs can be used to detect epistatic selection for fitness. Here we corroborate the theory by investigating genome-wide zygotic LDs in HapMap phase III human populations. Results show that non-Africa populations have much more significant zygotic LDs than do Africa populations. Africa populations (ASW, LWK, MKK, and YRI) possess more significant zygotic LDs for the double-homozygotes (DAABB) than any other significant zygotic LDs (DAABb, DAaBB, and DAaBb), while non-Africa populations generally have more significant DAaBb's than any other significant zygotic LDs (DAABB, DAABb, and DAaBB). Average r-squares for any significant zygotic LDs increase generally in an order of populations YRI, MKK, CEU, CHB, LWK, JPT, CHD, TSI, GIH, ASW, and MEX. Average r-squares are greater for DAABB and DAaBb than for DAaBB and DAABb in each population. YRI and MKK can be separated from LWK and ASW in terms of the pattern of average r-squares. All population divergences in zygotic LDs can be interpreted with the model of Out of Africa for modern human origins. We have also detected 19735-95921 SNP pairs exhibiting strong signals of epistatic selection in different populations. Gene-gene interactions for some epistatic SNP pairs are evident from empirical findings, but many more epistatic SNP pairs await evidence. Common epistatic SNP pairs rarely exist among all populations, but exist in distinct regions (Africa, Europe, and East Asia), which helps to understand geographical genomic medicine.
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spelling doaj.art-14ac53b350ea4501baa6a6f119232ea22022-12-21T21:31:51ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01106e013103910.1371/journal.pone.0131039Genomic Scans of Zygotic Disequilibrium and Epistatic SNPs in HapMap Phase III Populations.Xin-Sheng HuYang HuPrevious theory indicates that zygotic linkage disequilibrium (LD) is more informative than gametic or composite digenic LD in revealing natural population history. Further, the difference between the composite digenic and maximum zygotic LDs can be used to detect epistatic selection for fitness. Here we corroborate the theory by investigating genome-wide zygotic LDs in HapMap phase III human populations. Results show that non-Africa populations have much more significant zygotic LDs than do Africa populations. Africa populations (ASW, LWK, MKK, and YRI) possess more significant zygotic LDs for the double-homozygotes (DAABB) than any other significant zygotic LDs (DAABb, DAaBB, and DAaBb), while non-Africa populations generally have more significant DAaBb's than any other significant zygotic LDs (DAABB, DAABb, and DAaBB). Average r-squares for any significant zygotic LDs increase generally in an order of populations YRI, MKK, CEU, CHB, LWK, JPT, CHD, TSI, GIH, ASW, and MEX. Average r-squares are greater for DAABB and DAaBb than for DAaBB and DAABb in each population. YRI and MKK can be separated from LWK and ASW in terms of the pattern of average r-squares. All population divergences in zygotic LDs can be interpreted with the model of Out of Africa for modern human origins. We have also detected 19735-95921 SNP pairs exhibiting strong signals of epistatic selection in different populations. Gene-gene interactions for some epistatic SNP pairs are evident from empirical findings, but many more epistatic SNP pairs await evidence. Common epistatic SNP pairs rarely exist among all populations, but exist in distinct regions (Africa, Europe, and East Asia), which helps to understand geographical genomic medicine.https://doi.org/10.1371/journal.pone.0131039
spellingShingle Xin-Sheng Hu
Yang Hu
Genomic Scans of Zygotic Disequilibrium and Epistatic SNPs in HapMap Phase III Populations.
PLoS ONE
title Genomic Scans of Zygotic Disequilibrium and Epistatic SNPs in HapMap Phase III Populations.
title_full Genomic Scans of Zygotic Disequilibrium and Epistatic SNPs in HapMap Phase III Populations.
title_fullStr Genomic Scans of Zygotic Disequilibrium and Epistatic SNPs in HapMap Phase III Populations.
title_full_unstemmed Genomic Scans of Zygotic Disequilibrium and Epistatic SNPs in HapMap Phase III Populations.
title_short Genomic Scans of Zygotic Disequilibrium and Epistatic SNPs in HapMap Phase III Populations.
title_sort genomic scans of zygotic disequilibrium and epistatic snps in hapmap phase iii populations
url https://doi.org/10.1371/journal.pone.0131039
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