On detecting incomplete soft or hard selective sweeps using haplotype structure

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On detecting incomplete soft or hard selective sweeps using haplotype structure. / Ferrer-Admetlla, Anna; Liang, Mason; Korneliussen, Thorfinn Sand; Nielsen, Rasmus.

In: Molecular Biology and Evolution, Vol. 31, No. 5, 2014, p. 1275-1291.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Ferrer-Admetlla, A, Liang, M, Korneliussen, TS & Nielsen, R 2014, 'On detecting incomplete soft or hard selective sweeps using haplotype structure', Molecular Biology and Evolution, vol. 31, no. 5, pp. 1275-1291. https://doi.org/10.1093/molbev/msu077

APA

Ferrer-Admetlla, A., Liang, M., Korneliussen, T. S., & Nielsen, R. (2014). On detecting incomplete soft or hard selective sweeps using haplotype structure. Molecular Biology and Evolution, 31(5), 1275-1291. https://doi.org/10.1093/molbev/msu077

Vancouver

Ferrer-Admetlla A, Liang M, Korneliussen TS, Nielsen R. On detecting incomplete soft or hard selective sweeps using haplotype structure. Molecular Biology and Evolution. 2014;31(5):1275-1291. https://doi.org/10.1093/molbev/msu077

Author

Ferrer-Admetlla, Anna ; Liang, Mason ; Korneliussen, Thorfinn Sand ; Nielsen, Rasmus. / On detecting incomplete soft or hard selective sweeps using haplotype structure. In: Molecular Biology and Evolution. 2014 ; Vol. 31, No. 5. pp. 1275-1291.

Bibtex

@article{f435ef893d4e413b8090ba8ef0c44eb8,
title = "On detecting incomplete soft or hard selective sweeps using haplotype structure",
abstract = "We present a new haplotype-based statistic (nSL) for detecting both soft and hard sweeps in population genomic data from a single population. We compare our new method with classic single-population haplotype and site frequency spectrum (SFS)-based methods and show that it is more robust, particularly to recombination rate variation. However, all statistics show some sensitivity to the assumptions of the demographic model. Additionally, we show that nSL has at least as much power as other methods under a number of different selection scenarios, most notably in the cases of sweeps from standing variation and incomplete sweeps. This conclusion holds up under a variety of demographic models. In many aspects, our new method is similar to the iHS statistic; however, it is generally more robust and does not require a genetic map. To illustrate the utility of our new method, we apply it to HapMap3 data and show that in the Yoruban population, there is strong evidence of selection on genes relating to lipid metabolism. This observation could be related to the known differences in cholesterol levels, and lipid metabolism more generally, between African Americans and other populations. We propose that the underlying causes for the selection on these genes are pleiotropic effects relating to blood parasites rather than their role in lipid metabolism.",
author = "Anna Ferrer-Admetlla and Mason Liang and Korneliussen, {Thorfinn Sand} and Rasmus Nielsen",
year = "2014",
doi = "10.1093/molbev/msu077",
language = "English",
volume = "31",
pages = "1275--1291",
journal = "Molecular Biology and Evolution",
issn = "0737-4038",
publisher = "Oxford University Press",
number = "5",

}

RIS

TY - JOUR

T1 - On detecting incomplete soft or hard selective sweeps using haplotype structure

AU - Ferrer-Admetlla, Anna

AU - Liang, Mason

AU - Korneliussen, Thorfinn Sand

AU - Nielsen, Rasmus

PY - 2014

Y1 - 2014

N2 - We present a new haplotype-based statistic (nSL) for detecting both soft and hard sweeps in population genomic data from a single population. We compare our new method with classic single-population haplotype and site frequency spectrum (SFS)-based methods and show that it is more robust, particularly to recombination rate variation. However, all statistics show some sensitivity to the assumptions of the demographic model. Additionally, we show that nSL has at least as much power as other methods under a number of different selection scenarios, most notably in the cases of sweeps from standing variation and incomplete sweeps. This conclusion holds up under a variety of demographic models. In many aspects, our new method is similar to the iHS statistic; however, it is generally more robust and does not require a genetic map. To illustrate the utility of our new method, we apply it to HapMap3 data and show that in the Yoruban population, there is strong evidence of selection on genes relating to lipid metabolism. This observation could be related to the known differences in cholesterol levels, and lipid metabolism more generally, between African Americans and other populations. We propose that the underlying causes for the selection on these genes are pleiotropic effects relating to blood parasites rather than their role in lipid metabolism.

AB - We present a new haplotype-based statistic (nSL) for detecting both soft and hard sweeps in population genomic data from a single population. We compare our new method with classic single-population haplotype and site frequency spectrum (SFS)-based methods and show that it is more robust, particularly to recombination rate variation. However, all statistics show some sensitivity to the assumptions of the demographic model. Additionally, we show that nSL has at least as much power as other methods under a number of different selection scenarios, most notably in the cases of sweeps from standing variation and incomplete sweeps. This conclusion holds up under a variety of demographic models. In many aspects, our new method is similar to the iHS statistic; however, it is generally more robust and does not require a genetic map. To illustrate the utility of our new method, we apply it to HapMap3 data and show that in the Yoruban population, there is strong evidence of selection on genes relating to lipid metabolism. This observation could be related to the known differences in cholesterol levels, and lipid metabolism more generally, between African Americans and other populations. We propose that the underlying causes for the selection on these genes are pleiotropic effects relating to blood parasites rather than their role in lipid metabolism.

U2 - 10.1093/molbev/msu077

DO - 10.1093/molbev/msu077

M3 - Journal article

C2 - 24554778

VL - 31

SP - 1275

EP - 1291

JO - Molecular Biology and Evolution

JF - Molecular Biology and Evolution

SN - 0737-4038

IS - 5

ER -

ID: 104081783