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 …

Background The maturing field of genomics is rapidly increasing the number of sequenced
genomes and producing more information from those previously sequenced. Much of this …

Abstract The Ensembl project (https://www. ensembl. org) makes key genomic data sets
available to the entire scientific community without restrictions. Ensembl seeks to be a …

Most genomic variants associated with phenotypic traits or disease do not fall within gene
coding regions, but in regulatory regions, rendering their interpretation difficult. We collected …

Abstract The Ensembl (https://www. ensembl. org) is a system for generating and distributing
genome annotation such as genes, variation, regulation and comparative genomics across …

Ensembl (http://www. ensembl. org/) is a bioinformatics project to organize biological
information around the sequences of large genomes. It is a comprehensive source of stable …

The Ensembl project has been aggregating, processing, integrating and redistributing
genomic datasets since the initial releases of the draft human genome, with the aim of …

Abstract Ensembl Genomes (http://www. ensemblgenomes. org) is an integrating resource
for genome-scale data from non-vertebrate species, complementing the resources for …

Abstract The Ensembl project (https://www. ensembl. org) annotates genomes and
disseminates genomic data for vertebrate species. We create detailed and comprehensive …

The EnsMart system (www. ensembl. org/EnsMart) provides a generic data warehousing
solution for fast and flexible querying of large biological data sets and integration with third …