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10.3168/JDSC.2020-0048

Additionally, we conducted whole-genome association analysis to identify SNP and genes associated with vitamin B12 and transcobalamin.

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10.1093/gigascience/giab066

We found that the Supernova Assembly contained the full genome and was a suitable reference for RNAseq and single-nucleotide polymorphism calling, but the chromosome-level scaffolds provided by the addition of HiC data allowed synteny and whole-genome association mapping analyses.

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10.1016/J.MGENE.2021.100869

This study investigated factors affecting statistical power to detect causal variants and heritability in GWAS using sequencing data or a whole-genome association study (WGAS).

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10.1016/j.molp.2021.05.014

We present a costed proposal detailing how the interacting molecular components governing disease resistance could be captured from both the host and pathogen through biparental mapping, mutational genomics and whole-genome association genetics.

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10.4103/ccd.ccd_329_20

Genotype distribution was used to calculate the Hardy–Weinberg equilibrium using PLINK, a whole-genome association analysis toolset.

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10.1080/00071668.2019.1655710

A previous whole-genome association analysis has identified the motilin receptor gene (MLNR), which regulates gastrointestinal motility and gastric emptying, as a candidate gene related to chicken growth.

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10.18699/VJ19.525

Whole-genome association studies of Russian cattle breeds pointed to a novel gene which could be related to the “white-faced” phenotype and to a gene which is related to body temperature support under the acute cold stress.

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10.1016/b978-0-12-801496-7.00013-7

Whole-genome association studies in the general population have revealed genetic factors associated with metabolic disorders (i.

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10.1071/RDV31N1AB155

Whole-genome association study (GWAS) analysis, performed using molecular inbreeding as co-factor, revealed 8 SNP, located on chromosomes BTA2, BTA5, BTA7, and BTA11, significantly associated with sperm head regularity and rugosity.

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10.1038/s41398-019-0397-6

We herein report whole-genome association and rare-variant analyses on AUD traits in American Indians (AI) and European Americans (EA).

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10.1097/MOG.0000000000000509

Recent findings Whole-genome association studies in biliary atresia patients identified four distinct predisposition loci with four different genes potentially involved in the disease occurrence.

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Rare Variant Association D Association Crystallographic Association Causal Association Leukemia Association Variant Association Urology Association European Association Mycorrhizal Association Epigenome Wide Association Station Association Production Association Urooncology Association Nurses Association Spatial Association Il Association French Association Selective Association Papillomavirus Association China Association Habitat Association Factors Association Improved Association Membrane Association Spatial Numerical Association Time Dependent Association Novel Association Trait Association Investigating Association Determine Association Examining Association Identified Association Putative Association Injury Association Brand Association Dangerous Association Gene Association J Shaped Association Cell Association Genomewide Association Genomic Association En Association Uncommon Association Women Association Education Association Inverse Association Leur Association Particle Association Expression Association Strong Association Explore More

Whole Genome Association

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Aug 14, 2022

What is/are Whole Genome Association?

Whole Genome Association - Additionally, we conducted whole-genome association analysis to identify SNP and genes associated with vitamin B12 and transcobalamin. ^[1] We found that the Supernova Assembly contained the full genome and was a suitable reference for RNAseq and single-nucleotide polymorphism calling, but the chromosome-level scaffolds provided by the addition of HiC data allowed synteny and whole-genome association mapping analyses. ^[2] This study investigated factors affecting statistical power to detect causal variants and heritability in GWAS using sequencing data or a whole-genome association study (WGAS). ^[3] We present a costed proposal detailing how the interacting molecular components governing disease resistance could be captured from both the host and pathogen through biparental mapping, mutational genomics and whole-genome association genetics. ^[4] Genotype distribution was used to calculate the Hardy–Weinberg equilibrium using PLINK, a whole-genome association analysis toolset. ^[5] A previous whole-genome association analysis has identified the motilin receptor gene (MLNR), which regulates gastrointestinal motility and gastric emptying, as a candidate gene related to chicken growth. ^[6] Whole-genome association studies of Russian cattle breeds pointed to a novel gene which could be related to the “white-faced” phenotype and to a gene which is related to body temperature support under the acute cold stress. ^[7] Whole-genome association studies in the general population have revealed genetic factors associated with metabolic disorders (i. ^[8] Whole-genome association study (GWAS) analysis, performed using molecular inbreeding as co-factor, revealed 8 SNP, located on chromosomes BTA2, BTA5, BTA7, and BTA11, significantly associated with sperm head regularity and rugosity. ^[9] We herein report whole-genome association and rare-variant analyses on AUD traits in American Indians (AI) and European Americans (EA). ^[10] Recent findings Whole-genome association studies in biliary atresia patients identified four distinct predisposition loci with four different genes potentially involved in the disease occurrence. ^[11]