Evidence map›Paper›PMID 22883143›Full record

ArticleAmerican journal of human genetics2012

Genomic patterns of homozygosity in worldwide human populations.

Trevor J Pemberton, Devin Absher, Marcus W Feldman, Richard M Myers, Noah A Rosenberg, Jun Z Li

Abstract read
In one paragraph

Article in American journal of human genetics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 312 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
312citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

312 citing papers in PubMed, 1 synthesis or guideline pooled it.

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252 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Trevor J PembertonDepartment of Biology, Stanford University, Stanford, CA 94305, USA. trevorp@stanford.edu
Devin Absher
Marcus W Feldman
Richard M Myers
Noah A Rosenberg
Jun Z Li

Funding

Population genetics for large-scale sequencing studies of diverse populationsR01HG005855 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Noah Rosenberg, Paul A Scheet · 2010 to 2026
$5.8M
POPULATION GENETICS THEORYR01GM028016 · NIGMS · STANFORD UNIVERSITY · PI FELDMAN, MARCUS W · 1985 to 2010
$2.5M
Population-Genetic Studies for Association MappingR01GM081441 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ROSENBERG, NOAH · 2007 to 2011
$1.7M
NHGRI NIH HHS HG005855NHGRI NIH HHS R01 HG005855NIGMS NIH HHS GM081441NIGMS NIH HHS GM28016NIGMS NIH HHS R01 GM028016NIGMS NIH HHS R01 GM081441
6 · The paper itself

Abstract

Genome-wide patterns of homozygosity runs and their variation across individuals provide a valuable and often untapped resource for studying human genetic diversity and evolutionary history. Using genotype data at 577,489 autosomal SNPs, we employed a likelihood-based approach to identify runs of homozygosity (ROH) in 1,839 individuals representing 64 worldwide populations, classifying them by length into three classes-short, intermediate, and long-with a model-based clustering algorithm. For each class, the number and total length of ROH per individual show considerable variation across individuals and populations. The total lengths of short and intermediate ROH per individual increase with the distance of a population from East Africa, in agreement with similar patterns previously observed for locus-wise homozygosity and linkage disequilibrium. By contrast, total lengths of long ROH show large interindividual variations that probably reflect recent inbreeding patterns, with higher values occurring more often in populations with known high frequencies of consanguineous unions. Across the genome, distributions of ROH are not uniform, and they have distinctive continental patterns. ROH frequencies across the genome are correlated with local genomic variables such as recombination rate, as well as with signals of recent positive selection. In addition, long ROH are more frequent in genomic regions harboring genes associated with autosomal-dominant diseases than in regions not implicated in Mendelian diseases. These results provide insight into the way in which homozygosity patterns are produced, and they generate baseline homozygosity patterns that can be used to aid homozygosity mapping of genes associated with recessive diseases.

Indexed as

AlgorithmsGenetic VariationHomozygoteChromosome MappingCluster AnalysisGenes, RecessiveGenome, HumanGenomicsGenotypeGeographyHumansLikelihood FunctionsModels, GeneticPolymorphism, Single Nucleotide

Identifiers

PMID22883143
PMCPMC3415543

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.