Long runs of homozygosity are enriched for deleterious variation. - Wikidata - wikimedia - TriplyDB

Long runs of homozygosity are enriched for deleterious variation.

Long runs of homozygosity are enriched for deleterious variation.

http://www.wikidata.org/entity/Q37010445

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Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals Runs of Homozygosity: Association with Coronary Artery Disease and Gene Expression in Monocytes and Macrophages A time transect of exomes from a Native American population before and after European contact Genetics of Type 2 Diabetes: the Power of Isolated Populations.CATCHing putative causative variants in consanguineous families Excess of homozygosity in the major histocompatibility complex in schizophrenia.Commonalities in Development of Pure Breeds and Population Isolates Revealed in the Genome of the Sardinian Fonni's Dog Assessment of autozygosity in Nellore cows (Bos indicus) through high-density SNP genotypes.Using genome-wide measures of coancestry to maintain diversity and fitness in endangered and domestic pig populations Genome-wide analysis of signatures of selection in populations of African honey bees (Apis mellifera) using new web-based tools Estimation of inbreeding using pedigree, 50k SNP chip genotypes and full sequence data in three cattle breeds.Runs of homozygosity and distribution of functional variants in the cattle genome Homozygous loss-of-function variants in European cosmopolitan and isolate populations Long contiguous stretches of homozygosity spanning shortly the imprinted loci are associated with intellectual disability, autism and/or epilepsy.QueryOR: a comprehensive web platform for genetic variant analysis and prioritization Measuring individual inbreeding in the age of genomics: marker-based measures are better than pedigrees Whole-exome sequencing to analyze population structure, parental inbreeding, and familial linkage.Estimating the mutation load in human genomes A genome-wide perspective about the diversity and demographic history of seven Spanish goat breeds.Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery.Population growth inflates the per-individual number of deleterious mutations and reduces their mean effect.Association between autozygosity and major depression: stratification due to religious assortment Structural and genomic variation in preterm birth.Characterization and management of long runs of homozygosity in parental nucleus lines and their associated crossbred progeny The supposed tumor suppressor gene WWOX is mutated in an early lethal microcephaly syndrome with epilepsy, growth retardation and retinal degeneration.A model-based approach to characterize individual inbreeding at both global and local genomic scales.Detection and quantification of inbreeding depression for complex traits from SNP data.Estimation of Recent and Ancient Inbreeding in a Small Endogamous Tunisian Community Through Genomic Runs of Homozygosity.GARLIC: Genomic Autozygosity Regions Likelihood-based Inference and Classification.Runs of homozygosity: current knowledge and applications in livestock.Comorbidity in the Tunisian population.Heterozygosity Ratio, a Robust Global Genomic Measure of Autozygosity and Its Association with Height and Disease Risk Exome sequencing in schizophrenic patients with high levels of homozygosity identifies novel and extremely rare mutations in the GABA/glutamatergic pathways Characteristics of neutral and deleterious protein-coding variation among individuals and populations.Haplotype phasing after joint estimation of recombination and linkage disequilibrium in breeding populations.Consanguinity Rates Predict Long Runs of Homozygosity in Jewish Populations.Weighted likelihood inference of genomic autozygosity patterns in dense genotype data.Genome-wide Ancestry and Demographic History of African-Descendant Maroon Communities from French Guiana and Suriname.Age-based partitioning of individual genomic inbreeding levels in Belgian Blue cattle.Loss-of-Function Variants in MYLK Cause Recessive Megacystis Microcolon Intestinal Hypoperistalsis Syndrome.

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Long runs of homozygosity are enriched for deleterious variation.

http://www.wikidata.org/entity/Q37010445

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

@pt

bilimsel makale

@tr

scientific article published on 06 June 2013

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Long runs of homozygosity are enriched for deleterious variation.

@en

Long runs of homozygosity are enriched for deleterious variation.

@nl

type

label

Long runs of homozygosity are enriched for deleterious variation.

@en

Long runs of homozygosity are enriched for deleterious variation.

@nl

prefLabel

Long runs of homozygosity are enriched for deleterious variation.

@en

Long runs of homozygosity are enriched for deleterious variation.

@nl

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J.AJHG.2013.05.003

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American Journal of Human Genetics

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Long runs of homozygosity are enriched for deleterious variation.

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Jishu Xu

http://www.w3.org/2001/XMLSchema#string

Jun Z Li

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Noah A Rosenberg

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Sebastian Zöllner

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Trevor J Pemberton

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Weiping Peng

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Zachary A Szpiech

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P2860

A systematic approach to mapping recessive disease genes in individuals from outbred populations

An integrated map of genetic variation from 1,092 human genomes

Long homozygous chromosomal segments in reference families from the centre d'Etude du polymorphisme humain

Support from the relationship of genetic and geographic distance in human populations for a serial founder effect originating in Africa

Runs of homozygosity in European populations

A second generation human haplotype map of over 3.1 million SNPs

Global distribution of genomic diversity underscores rich complex history of continental human populations

Fast and accurate short read alignment with Burrows-Wheeler transform

The consensus coding sequence (CCDS) project: Identifying a common protein-coding gene set for the human and mouse genomes

The genetics of inbreeding depression

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10.1016/J.AJHG.2013.05.003

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