筛选
科学数据
统计数据
共检索到249条 ,权限内显示50条;
Data from: Population scale mapping of transposable element diversity reveals links to gene regulation and epigenomic variation
- 负责人：
- DOI：
- doi:10.5061/dryad.187b3
- 摘要：
- e not in linkage disequilibrium with nearby SNPs, implicating these variants as a source of novel genetic diversity. Many common TE variants were associated with significant
Data from: Frequency and distribution of 152 genetic disease variants in over 100,000 mixed breed and purebred dogs
- 负责人：
- Donner, Jonas
- DOI：
- doi:10.5061/dryad.dd91b
- 摘要：
- . Limited data on frequencies of genetic disease variants across breeds exists, and the disease heritage of mixed breed dogs remains poorly explored to dat
Data from: SSR-marker analysis of the intracultivar phenotypic variation discovered within 3 soybean cultivars
- 负责人：
- Yates, Jennifer L.
- DOI：
- doi:10.5061/dryad.7dn526gq
- 摘要：
- Benning had 34 variant alleles, and the seven lines from Cook had 34 variant alleles, therefore, possessing unique genetic fingerprints. Most of the int
Data from: Exome-chip association analysis of intracranial aneurysms
- 负责人：
- DOI：
- doi:10.5061/dryad.099bk53
- 摘要：
- Objective: To investigate to what extent low-frequency genetic variants (with minor allele frequencies <5%) affect the risk of intracranial ane
Data from: Identification of genetic defects in 33 probands with Stargardt disease by WES-based bioinformatics gene panel analysis
- 负责人：
- DOI：
- doi:10.5061/dryad.0qk7f
- 摘要：
- were selected from all known genes associated with hereditary retinal dystrophy and then confirmed by Sanger sequencing. Putative pathogenic variants
Data from: Unique features of germline variation in five Egyptian familial breast cancer families revealed by exome sequencing
- 负责人：
- DOI：
- doi:10.5061/dryad.p236p
- 摘要：
- ng whole exome sequencing, we investigated genetic predisposition in five Egyptian familial breast cancer families. No pathogenic variants in BRCA1, BRCA2 and other classic
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：
- on 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: The evolution of novel host use is unlikely to be constrained by tradeoffs or a lack of genetic variation
- 负责人：
- DOI：
- doi:10.5061/dryad.7b5m7
- 摘要：
- basis. We documented very few genetic variants with trade-offs that would inherently constrain diet breadth by preventing the optimization of performance
Data from: Genome-wide association meta-analysis of functional outcome after ischemic stroke
- 负责人：
- DOI：
- doi:10.5061/dryad.s38kf65
- 摘要：
- Objective: To discover common genetic variants associated with post-stroke outcomes using a genome-wide association (GWA) study. Methods
Data from: Loss of paraplegin drives spasticity rather than ataxia in a cohort of 241 patients with SPG7
- 负责人：
- DOI：
- doi:10.5061/dryad.sb4kr01
- 摘要：
- er cohort of patients with spastic paraplegia gene 7 (SPG7). Methods: We analyzed clinical and genetic data from 241 patients with SPG7, integrati
