-
Federal
Database of Short Genetic Variations (dbSNP)
U.S. Department of Health & Human Services —
Database of Short Genetic Variations (dbSNP) contains human single nucleotide variations, microsatellites, and small-scale insertions and deletions along with... -
Federal
NCBI Virus
U.S. Department of Health & Human Services —
NCBI Virus is an integrative, value-added resource designed to support retrieval, display and analysis of a curated collection of virus sequences and large sequence... -
Federal
GEO (Gene Expression Omnibus)
U.S. Department of Health & Human Services —
GEO (Gene Expression Omnibus) is a public functional genomics data repository supporting MIAME-compliant data submissions. There are also tools provided to help users... -
Federal
Database of Genotype and Phenotype (dbGaP)
U.S. Department of Health & Human Services —
Database of Genotype and Phenotype (dbGaP) was developed to archive and distribute the data and results from studies that have investigated the interaction of... -
Federal
Open Reading Frame Finder (ORF Finder)
U.S. Department of Health & Human Services —
A graphical analysis tool that finds all open reading frames in a user's sequence or in a sequence already in the database. -
Federal
OMIM (Online Mendelian Inheritance in Man)
U.S. Department of Health & Human Services —
Comprehensive, authoritative, and timely compendium of human genes and genetic phenotypes. -
Federal
Genetic Testing Registry (GTR)
U.S. Department of Health & Human Services —
Genetic Testing Registry (GTR) is a free, centralized voluntary registry of comprehensive genetic test information covering clinical and research tests for Mendelian... -
Federal
SPDI Variation Service
U.S. Department of Health & Human Services —
This genetic variation services interconvert and transform short genetic variants between HGVS expressions, VCF format, and the new SPDI (Sequence Position Deletion... -
Federal
Transcriptome Shotgun Assembly (TSA) Sequence Database and Submissions
U.S. Department of Health & Human Services —
TSA is an archive of computationally assembled transcript sequences from primary data such as ESTs and Next Generation Sequencing Technologies. The overlapping... -
Federal
Phenotype-Genotype Integrator (PheGenI)
U.S. Department of Health & Human Services —
Supports finding human phenotype/genotype relationships with queries by phenotype, chromosome location, gene, and SNP identifiers. Currently includes information from... -
Federal
HomoloGene
U.S. Department of Health & Human Services —
System for automated detection of homologs among the annotated genes of several completely sequenced eukaryotic genomes. -
Federal
BioProject
U.S. Department of Health & Human Services —
The BioProject database links to data that have been or will be deposited into archival databases maintained at members of the International Nucleotide Sequence... -
Federal
GRAF (Genetic Relationship and Fingerprinting)
U.S. Department of Health & Human Services —
GRAF (Genetic Relationship and Fingerprinting) is a C++ program that quickly finds the closely related subjects, infers subject ancestry, determines subject sexes... -
Federal
RefSeq: NCBI Reference Sequence Database
U.S. Department of Health & Human Services —
A comprehensive, integrated, non-redundant, well-annotated set of reference sequences including genomic, transcript, and protein.