HIV-1, Human Protein Interaction DatabaseĪ database of known interactions of HIV-1 proteins with proteins from human hosts. At the GRC website (), the public can view genomic regions currently under review, report genome-related problems and contact the GRC. In addition, the GRC seeks to provide alternate assemblies for complex or structurally variant genomic loci. The GRC works to correct misrepresented loci and to close remaining assembly gaps. Members consist of The Genome Center at Washington University, the Wellcome Trust Sanger Institute, the European Bioinformatics Institute (EBI) and the National Center for Biotechnology Information (NCBI). The Genome Reference Consortium (GRC) maintains responsibility for the human and mouse reference genomes. All three main domains of life (bacteria, archaea, and eukaryota) are represented, as well as many viruses, phages, viroids, plasmids, and organelles. The genomes represent both completely sequenced organisms and those for which sequencing is in progress. GenomeĬontains sequence and map data from the whole genomes of over 1000 organisms. In addition to archiving variation discovery, dbVar also stores associations of defined variants with phenotype information.
Clc sequence viewer restriction map archive#
The dbVar database has been developed to archive information associated with large scale genomic variation, including large insertions, deletions, translocations and inversions. Database of Genomic Structural Variation (dbVar) This resource describes project scope, material, and objectives and provides a mechanism to retrieve datasets that are often difficult to find due to inconsistent annotation, multiple independent submissions, and the varied nature of diverse data types which are often stored in different databases. BioProject (formerly Genome Project)Ī collection of genomics, functional genomics, and genetics studies and links to their resulting datasets. A database providing information on the structure of assembled genomes, assembly names and other meta-data, statistical reports, and links to genomic sequence data.
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