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Extent of genome-wide linkage disequilibrium in Australian Holstein-Friesian cattle based on a high-density SNP panel

Extent of genome-wide linkage disequilibrium in Australian Holstein-Friesian cattle based on a high-density SNP panel
Extent of genome-wide linkage disequilibrium in Australian Holstein-Friesian cattle based on a high-density SNP panel
BACKGROUND: The extent of linkage disequilibrium (LD) within a population determines the number of markers that will be required for successful association mapping and marker-assisted selection. Most studies on LD in cattle reported to date are based on microsatellite markers or small numbers of single nucleotide polymorphisms (SNPs) covering one or only a few chromosomes. This is the first comprehensive study on the extent of LD in cattle by analyzing data on 1,546 Holstein-Friesian bulls genotyped for 15,036 SNP markers covering all regions of all autosomes. Furthermore, most studies in cattle have used relatively small sample sizes and, consequently, may have had biased estimates of measures commonly used to describe LD. We examine minimum sample sizes required to estimate LD without bias and loss in accuracy. Finally, relatively little information is available on comparative LD structures including other mammalian species such as human and mouse, and we compare LD structure in cattle with public-domain data from both human and mouse. RESULTS: We computed three LD estimates, D', Dvol and r2, for 1,566,890 syntenic SNP pairs and a sample of 365,400 non-syntenic pairs. Mean D' is 0.189 among syntenic SNPs, and 0.105 among non-syntenic SNPs; mean r2 is 0.024 among syntenic SNPs and 0.0032 among non-syntenic SNPs. All three measures of LD for syntenic pairs decline with distance; the decline is much steeper for r2 than for D' and Dvol. The value of D' and Dvol are quite similar. Significant LD in cattle extends to 40 kb (when estimated as r2) and 8.2 Mb (when estimated as D'). The mean values for LD at large physical distances are close to those for non-syntenic SNPs. Minor allelic frequency threshold affects the distribution and extent of LD. For unbiased and accurate estimates of LD across marker intervals spanning 0.62). For estimation of LD by D' and Dvol with sufficient precision, a sample size of at least 400 is required, whereas for r2 a minimum sample of 75 is adequate.
genetics, cattle, single nucleotide, animals, synteny, design, australia, genome, male, sample size, gene frequency, polymorphism, reproduction, linkage disequilibrium, research support, research, chromosomes, human, humans, population, affect, mice
1471-2164
Khatkar, Mehar S.
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Nicholas, Mehar S.
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Collins, Andrew R.
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Zenger, Kyall R.
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Cavanagh, Julie A.L.
d8340e8b-fdd6-4cd0-b335-54cd37e87eb7
Barris, Wes
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Schnabel, Robert D.
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Taylor, Jeremy F.
05bfcea3-76fe-4a5b-9608-da690172e84e
Raadsma, Herman W.
57cc3516-ef70-4f4f-8944-68b761197e89
Khatkar, Mehar S.
6d414f73-925e-47f1-95ce-749a49d8e09e
Nicholas, Mehar S.
3c03ef6f-3576-4b00-9a09-a1b58730f099
Collins, Andrew R.
7daa83eb-0b21-43b2-af1a-e38fb36e2a64
Zenger, Kyall R.
b56e4990-7f69-47a5-b83f-9f567be1d0a1
Cavanagh, Julie A.L.
d8340e8b-fdd6-4cd0-b335-54cd37e87eb7
Barris, Wes
76eeac40-8907-4add-95a8-44fef644d02d
Schnabel, Robert D.
fb44f2e3-ce14-45bb-ac83-384cbc677be8
Taylor, Jeremy F.
05bfcea3-76fe-4a5b-9608-da690172e84e
Raadsma, Herman W.
57cc3516-ef70-4f4f-8944-68b761197e89

Khatkar, Mehar S., Nicholas, Mehar S., Collins, Andrew R., Zenger, Kyall R., Cavanagh, Julie A.L., Barris, Wes, Schnabel, Robert D., Taylor, Jeremy F. and Raadsma, Herman W. (2008) Extent of genome-wide linkage disequilibrium in Australian Holstein-Friesian cattle based on a high-density SNP panel. BMC Genomics, 9 (187). (doi:10.1186/1471-2164-9-187).

Record type: Article

Abstract

BACKGROUND: The extent of linkage disequilibrium (LD) within a population determines the number of markers that will be required for successful association mapping and marker-assisted selection. Most studies on LD in cattle reported to date are based on microsatellite markers or small numbers of single nucleotide polymorphisms (SNPs) covering one or only a few chromosomes. This is the first comprehensive study on the extent of LD in cattle by analyzing data on 1,546 Holstein-Friesian bulls genotyped for 15,036 SNP markers covering all regions of all autosomes. Furthermore, most studies in cattle have used relatively small sample sizes and, consequently, may have had biased estimates of measures commonly used to describe LD. We examine minimum sample sizes required to estimate LD without bias and loss in accuracy. Finally, relatively little information is available on comparative LD structures including other mammalian species such as human and mouse, and we compare LD structure in cattle with public-domain data from both human and mouse. RESULTS: We computed three LD estimates, D', Dvol and r2, for 1,566,890 syntenic SNP pairs and a sample of 365,400 non-syntenic pairs. Mean D' is 0.189 among syntenic SNPs, and 0.105 among non-syntenic SNPs; mean r2 is 0.024 among syntenic SNPs and 0.0032 among non-syntenic SNPs. All three measures of LD for syntenic pairs decline with distance; the decline is much steeper for r2 than for D' and Dvol. The value of D' and Dvol are quite similar. Significant LD in cattle extends to 40 kb (when estimated as r2) and 8.2 Mb (when estimated as D'). The mean values for LD at large physical distances are close to those for non-syntenic SNPs. Minor allelic frequency threshold affects the distribution and extent of LD. For unbiased and accurate estimates of LD across marker intervals spanning 0.62). For estimation of LD by D' and Dvol with sufficient precision, a sample size of at least 400 is required, whereas for r2 a minimum sample of 75 is adequate.

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Published date: 24 April 2008
Keywords: genetics, cattle, single nucleotide, animals, synteny, design, australia, genome, male, sample size, gene frequency, polymorphism, reproduction, linkage disequilibrium, research support, research, chromosomes, human, humans, population, affect, mice

Identifiers

Local EPrints ID: 59929
URI: http://eprints.soton.ac.uk/id/eprint/59929
ISSN: 1471-2164
PURE UUID: f67a10d4-4c69-4cd3-a8bb-3047bd8a482e
ORCID for Andrew R. Collins: ORCID iD orcid.org/0000-0001-7108-0771

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Date deposited: 23 Mar 2009
Last modified: 16 Mar 2024 02:42

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Contributors

Author: Mehar S. Khatkar
Author: Mehar S. Nicholas
Author: Kyall R. Zenger
Author: Julie A.L. Cavanagh
Author: Wes Barris
Author: Robert D. Schnabel
Author: Jeremy F. Taylor
Author: Herman W. Raadsma

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