Relatedness mapping and tracts of relatedness for genome-wide data in the presence of linkage disequilibrium

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Relatedness mapping and tracts of relatedness for genome-wide data in the presence of linkage disequilibrium. / Albrechtsen, Anders; Korneliussen, Thorfinn Sand; Moltke, Ida; van Overseem Hansen, Thomas; Nielsen, Finn Cilius; Nielsen, Rasmus.

In: Genetic Epidemiology, Vol. 33, No. 3, 2009, p. 266-274.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Albrechtsen, A, Korneliussen, TS, Moltke, I, van Overseem Hansen, T, Nielsen, FC & Nielsen, R 2009, 'Relatedness mapping and tracts of relatedness for genome-wide data in the presence of linkage disequilibrium', Genetic Epidemiology, vol. 33, no. 3, pp. 266-274. https://doi.org/10.1002/gepi.20378

APA

Albrechtsen, A., Korneliussen, T. S., Moltke, I., van Overseem Hansen, T., Nielsen, F. C., & Nielsen, R. (2009). Relatedness mapping and tracts of relatedness for genome-wide data in the presence of linkage disequilibrium. Genetic Epidemiology, 33(3), 266-274. https://doi.org/10.1002/gepi.20378

Vancouver

Albrechtsen A, Korneliussen TS, Moltke I, van Overseem Hansen T, Nielsen FC, Nielsen R. Relatedness mapping and tracts of relatedness for genome-wide data in the presence of linkage disequilibrium. Genetic Epidemiology. 2009;33(3):266-274. https://doi.org/10.1002/gepi.20378

Author

Albrechtsen, Anders ; Korneliussen, Thorfinn Sand ; Moltke, Ida ; van Overseem Hansen, Thomas ; Nielsen, Finn Cilius ; Nielsen, Rasmus. / Relatedness mapping and tracts of relatedness for genome-wide data in the presence of linkage disequilibrium. In: Genetic Epidemiology. 2009 ; Vol. 33, No. 3. pp. 266-274.

Bibtex

@article{a5cb6870f85611ddb219000ea68e967b,
title = "Relatedness mapping and tracts of relatedness for genome-wide data in the presence of linkage disequilibrium",
abstract = "Estimates of relatedness have several applications such as the identification of relatives or in identifying disease related genes through identity by descent (IBD) mapping. Here we present a new method for identifying IBD tracts among individuals from genome-wide single nucleotide polymorphisms data. We use a continuous time Markov model where the hidden states are the number of alleles shared IBD between pairs of individuals at a given position. In contrast to previous methods, our method accurately accounts for linkage disequilibrium using pairwise haplotype probabilities. The method provides a map of the local relatedness along the genome. We illustrate the potential of the method for mapping disease genes on a real data set, and show that the method has the potential to map causative disease mutations using only a handful of affected individuals. The new IBD mapping method provides considerable improvement in mapping power in natural populations compared to standard association mapping methods. Genet. Epidemiol. 2008. (c) 2008 Wiley-Liss, Inc.",
author = "Anders Albrechtsen and Korneliussen, {Thorfinn Sand} and Ida Moltke and {van Overseem Hansen}, Thomas and Nielsen, {Finn Cilius} and Rasmus Nielsen",
note = "Keywords identity by descent • relatedness • hidden Markov model • linkage • association • complex disease • genome-wide analysis • SNP",
year = "2009",
doi = "10.1002/gepi.20378",
language = "English",
volume = "33",
pages = "266--274",
journal = "Genetic Epidemiology",
issn = "0741-0395",
publisher = "JohnWiley & Sons, Inc.",
number = "3",

}

RIS

TY - JOUR

T1 - Relatedness mapping and tracts of relatedness for genome-wide data in the presence of linkage disequilibrium

AU - Albrechtsen, Anders

AU - Korneliussen, Thorfinn Sand

AU - Moltke, Ida

AU - van Overseem Hansen, Thomas

AU - Nielsen, Finn Cilius

AU - Nielsen, Rasmus

N1 - Keywords identity by descent • relatedness • hidden Markov model • linkage • association • complex disease • genome-wide analysis • SNP

PY - 2009

Y1 - 2009

N2 - Estimates of relatedness have several applications such as the identification of relatives or in identifying disease related genes through identity by descent (IBD) mapping. Here we present a new method for identifying IBD tracts among individuals from genome-wide single nucleotide polymorphisms data. We use a continuous time Markov model where the hidden states are the number of alleles shared IBD between pairs of individuals at a given position. In contrast to previous methods, our method accurately accounts for linkage disequilibrium using pairwise haplotype probabilities. The method provides a map of the local relatedness along the genome. We illustrate the potential of the method for mapping disease genes on a real data set, and show that the method has the potential to map causative disease mutations using only a handful of affected individuals. The new IBD mapping method provides considerable improvement in mapping power in natural populations compared to standard association mapping methods. Genet. Epidemiol. 2008. (c) 2008 Wiley-Liss, Inc.

AB - Estimates of relatedness have several applications such as the identification of relatives or in identifying disease related genes through identity by descent (IBD) mapping. Here we present a new method for identifying IBD tracts among individuals from genome-wide single nucleotide polymorphisms data. We use a continuous time Markov model where the hidden states are the number of alleles shared IBD between pairs of individuals at a given position. In contrast to previous methods, our method accurately accounts for linkage disequilibrium using pairwise haplotype probabilities. The method provides a map of the local relatedness along the genome. We illustrate the potential of the method for mapping disease genes on a real data set, and show that the method has the potential to map causative disease mutations using only a handful of affected individuals. The new IBD mapping method provides considerable improvement in mapping power in natural populations compared to standard association mapping methods. Genet. Epidemiol. 2008. (c) 2008 Wiley-Liss, Inc.

U2 - 10.1002/gepi.20378

DO - 10.1002/gepi.20378

M3 - Journal article

C2 - 19025785

VL - 33

SP - 266

EP - 274

JO - Genetic Epidemiology

JF - Genetic Epidemiology

SN - 0741-0395

IS - 3

ER -

ID: 10457557