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Data from: Population scale mapping of transposable element diversity reveals links to gene regulation and epigenomic variation
负责人:
关键词:
Arabidopsis;genomics;DNA methylation;Transposable elements;epigenetics
DOI:
doi:10.5061/dryad.187b3
摘要:
ified 23,095 TE presence/absence variants between 216 Arabidopsis accessions. Most TE variants were rare, and we find these rare variants associa
Data from: The standing pool of genomic structural variation in a natural population of Mimulus guttatus
负责人:
关键词:
structural variation;natural selection;population genomics;Mimulus nasutus;indel;Mimulus guttatus
DOI:
doi:10.5061/dryad.41dq8
摘要:
tion in a species, and understanding how these different forms of genetic variation interact with natural selection. Recent work has shown that structural variants
Data from: Frequency and distribution of 152 genetic disease variants in over 100,000 mixed breed and purebred dogs
负责人:
Donner, Jonas
关键词:
dog canine Mendelian disease genotypes panel screening
DOI:
doi:10.5061/dryad.dd91b
摘要:
in the generated data. We identified the most prevalent, and rare, disease susceptibility variants across the general dog population while providing the fir
Data from: Gene-wise association of variants in four lysosomal storage disorder genes in neuropathologically confirmed Lewy Body disease
负责人:
关键词:
rare variants;Lysosomal Storage Disorder;Gene wise association;Lewy Body Disease
DOI:
doi:10.5061/dryad.61c8t
摘要:
(n = 4), PD (n = 9) and control brains (n = 17), comparing GBA mutation carriers to non-carriers. Results: In a ‘gene-wise’ analysis, variants in GBA, SMPD1
Data from: Genome-wide meta-analysis of sciatica in Finnish population
负责人:
关键词:
DOI:
doi:10.5061/dryad.tq5f0
摘要:
e led to enrichment of certain rare and low frequency variants. We performed here the first genome-wide association (GWAS) and meta-analysis of scia
Data from: Assessing gene-environment interactions for common and rare variants with binary traits using gene-trait similarity regression
负责人:
关键词:
GLMM;Binary traits;Rare variant association;gene-environment interaction;Marker-set interaction analysis;Variance-Component Methods
DOI:
doi:10.5061/dryad.742gv
摘要:
s, and interactions are sensitive to misspecification of the main effects model. These issues are exacerbated when working with binary phenotypes and rare variants
Data from: Joint prediction of multiple quantitative traits using a Bayesian multivariate antedependence model
负责人:
关键词:
whole-genome prediction simulation data
DOI:
doi:10.5061/dryad.dd60v
摘要:
to deal with missing phenotypes and resequence data with rare variants, offering a feasible way to jointly predict phenotypes for multiple complex tra
Data from: Whole genome sequencing and rare variant analysis in essential tremor families
负责人:
关键词:
Essential tremor;Susceptibility Gene;calcium channel;copy number variants;Homo Sapiens;rare variants;SLIT3;families;axon guidance;risk factor;whole genome sequencing;CACNA1G
DOI:
doi:10.5061/dryad.td8d20v
摘要:
of functional rare coding and non-coding variants may explain the heritability of ET. We performed WGS in eight ET families (n=40 individuals) enrolled
Data from: The association between mitochondrial genetic variation and reduced colony fitness in an invasive wasp
负责人:
关键词:
mtDNA variation;Mitochondrial DNA;colony fitness;Vespula vulgaris;invasive species
DOI:
doi:10.5061/dryad.17jn0fq
摘要:
mitochondrial function was detected. We discuss how detected variants may alter secondary structures, gene expression or mito-nuclear interactions, or could
Data from: Admixture and the organization of genetic diversity in a butterfly species complex revealed through common and rare genetic variants
负责人:
关键词:
Genomics\/Proteomics;hybridization;Lycaeides;speciation;Population Genetics - Empirical
DOI:
doi:10.5061/dryad.pq93h
摘要:
analyses indicate that multiple distinct admixed lineages or populations exist. We find that most genetic variants in Lycaeides are rare

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