.png){kind=icon}
.png){kind=icon}
Return
Ensembl variation resources
.png){kind=icon}
OA
AI
DOI：10.1093/database/bay119.png)
.png){kind=icon}
.png){kind=icon}
Share.png){kind=icon}
Save
Abstract
En 中文
The major goal of sequencing humans and many other species is to understand the link between genomic variation, phenotype and disease. There are numerous valuable and well-established variation resources, but collating and making sense of non-homogeneous, often large-scale data sets from disparate sources remains a challenge. Without a systematic catalogue of these data and appropriate query and annotation tools, understanding the genome sequence of an individual and assessing their disease risk is impossible. In Ensembl, we substantially solve this problem: we develop methods to facilitate data integration and broad access; aggregate information in a consistent manner and make it available a variety of standard formats, both visually and programmatically; build analysis pipelines to compare variants to comprehensive genomic annotation sets; and make all tools and data publicly available.
Keywords:
ONLINE MENDELIAN INHERITANCE
SEQUENCE VARIANTS
DATABASE
GENOMES
ASSOCIATION
PROJECT
REPOSITORY
PHENOTYPE
PLATFORM
CATALOG
AI Summary
Key information extracted from the uploaded paper, including a brief overview, abstract, background, key highlights, visual analysis, and future outlook.
Journal
D
IF:
3.6
Papers:
1.7K
Citations:
6.1K