Results 1 to 10 of about 7,409,346 (224)
GemTools: A fast and efficient approach to estimating genetic ancestry [PDF]
To uncover the genetic basis of complex disease, individuals are often measured at a large number of genetic variants (usually SNPs) across the genome. GemTools provides computationally efficient tools for modeling genetic ancestry based on SNP genotypes.
Devlin, Bernie+4 more
arxiv +3 more sources
Monitoring of environmental gases and calf health in Italian Mediterranean buffalo herd
In buffalo breeding, calves require special attention and housing systems that provide thermal comfort, good air quality, brightness, and adequate space.
Simona Leonetti +4 more
doaj +1 more source
During the past three years, the national prevention and control policies for coronavirus disease 2019(COVID-19) have gone from'Class A control' to 'Class B control'.
Clinical Data and Biobank Committee of China Research Hospital Association+1 more
doaj +1 more source
LocusZoom.js: interactive and embeddable visualization of genetic association study results
LocusZoom.js is a JavaScript library for creating interactive web-based visualizations of genetic association study results. It can display one or more traits in the context of relevant biological data (such as gene models and other genomic annotation ...
Andrew P. Boughton+6 more
semanticscholar +1 more source
Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics [PDF]
Genetic association studies, in particular the genome-wide association study (GWAS) design, have provided a wealth of novel insights into the aetiology of a wide range of human diseases and traits, in particular cardiovascular diseases and lipid ...
C. Giambartolomei+6 more
semanticscholar +1 more source
Fine-mapping genetic associations [PDF]
AbstractWhilst thousands of genetic variants have been associated with human traits, identifying the subset of those variants that are causal requires a further ‘fine-mapping’ step. We review the basic fine-mapping approach, which is computationally fast and requires only summary data, but depends on an assumption of a single causal variant per ...
Hutchinson, Anna+2 more
openaire +3 more sources
Rare and common variant discovery by whole-genome sequencing of 101 Thoroughbred racehorses
The Thoroughbred breed was formed by crossing Oriental horse breeds and British native horses and is currently used in horseracing worldwide. In this study, we constructed a single-nucleotide variant (SNV) database using data from 101 Thoroughbred ...
Teruaki Tozaki+7 more
doaj +1 more source
Genetic risk factors for Parkinson's disease (PD) risk and progression have been identified from genome-wide association studies (GWAS), as well as studies of familial forms of PD, implicating common variants at more than 90 loci and pathogenic or likely
Katerina Markopoulou+12 more
doaj +1 more source
Background: Despite hypertension being highly prevalent in individuals with African-ancestry, they are under-represented in large genome-wide association studies.
S. Singh+6 more
doaj +1 more source
Introduction: When analyzing data from large-scale genetic association studies, such as targeted or genome-wide resequencing studies, it is common to assume a single genetic model, such as dominant or additive, for all tests of association between a ...
Camille M. Moore+2 more
semanticscholar +1 more source