(Q33773027)

29 July 2017

title

High-resolution detection of identity by descent in unrelated individuals (English)

1 reference

29 July 2017

1

Sharon R Browning

1 reference

29 July 2017

Brian L Browning

2

1 reference

29 July 2017

language of work or name

English

0 references

publication date

18 March 2010

1 reference

American Journal of Human Genetics

29 July 2017

published in

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29 July 2017

volume

86

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29 July 2017

issue

4

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29 July 2017

page(s)

526-539

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Simultaneous genotype calling and haplotype phasing improves genotype accuracy and reduces false-positive associations for genome-wide association studies

29 July 2017

cites work

1 reference

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Detection of sharing by descent, long-range phasing and haplotype imputation

4 July 2018

1 reference

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4 July 2018

1 reference

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Whole population, genome-wide mapping of hidden relatedness

4 July 2018

1 reference

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A SNP streak model for the identification of genetic regions identical-by-descent

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850444

Estimation of pairwise identity by descent from dense genetic marker data in a population sample of haplotypes

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850444

Shared genomic segment analysis. Mapping disease predisposition genes in extended pedigrees using SNP genotype assays.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850444

A second generation human haplotype map of over 3.1 million SNPs

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850444

Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering

4 July 2018

1 reference

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4 July 2018

1 reference

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Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

4 July 2018

1 reference

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Homozygosity haplotype allows a genomewide search for the autosomal segments shared among patients.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850444

Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals

4 July 2018

1 reference

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Multilocus association mapping using variable-length Markov chains

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850444

A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850444

A comparison of phasing algorithms for trios and unrelated individuals

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850444

Cohort profile: 1958 British birth cohort (National Child Development Study).

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850444

Estimation of the inbreeding coefficient through use of genomic data

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850444

Quantitative-trait homozygosity and association mapping and empirical genomewide significance in large, complex pedigrees: fasting serum-insulin level in the Hutterites

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850444

Statistical tests for detection of misspecified relationships by use of genome-screen data

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850444

Genetic analysis of simulated oligogenic traits in nuclear and extended pedigrees: summary of GAW10 contributions

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850444

Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2850444

Perspectives of identity by descent (IBD) mapping in founder populations

4 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20303063

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.AJHG.2010.02.021

1 reference

29 July 2017

1 reference

29 July 2017

1 reference