A design prototype by Datopian, not an official website
Find a Commonwealth ResourceHealthData.Gov
Background Horizontal gene transfer (HGT) played an important role in shaping microbial genomes. In addition to genes under sporadic selection, HGT also affects housekeeping genes and those involved in information…
Updated Oct 29, 2026
HealthData.Gov
A public domain quality assurance software package that facilitates the assessment of multiplex short tandem repeat (STR) DNA profiles based on laboratory-specific protocols.
Updated Oct 29, 2026
HealthData.Gov
Gene integrates information from a wide range of species. A record may include nomenclature, Reference Sequences (RefSeqs), maps, pathways, variations, phenotypes, and links to genome-, phenotype-, and locus-specific…
Updated Oct 29, 2026
HealthData.Gov
NIH Genetic sequence database; an annotated collection of all publicly available DNA sequences.
Updated Oct 29, 2026
HealthData.Gov
NCBI Datasets is one-stop shop for finding, browsing, and downloading genomic data. Find and download taxonomy, genome, gene, transcript, protein data, including installation of NCBI Datasets command-line tools.
Updated Oct 29, 2026
HealthData.Gov
GRAF (Genetic Relationship and Fingerprinting) is a C++ program that quickly finds the closely related subjects, infers subject ancestry, determines subject sexes using genotypes and compares the results derived from…
Updated Oct 29, 2026
HealthData.Gov
Comprehensive, authoritative, and timely compendium of human genes and genetic phenotypes.
Updated Oct 29, 2026
HealthData.Gov
Database of Genomic Structural Variation (dbVar) is NCBI's database of human genomic Structural Variation — large variants >50 bp including insertions, deletions, duplications, inversions, mobile elements,…
Updated Oct 29, 2026
HealthData.Gov
This site is for browsing WGS (Whole Genome Shotgun) genomes, TSA (Transcriptome Shotgun Assemblies) and TLS (Targeted Locus Study) sets. WGS sequences are incomplete genomes that have been sequenced by a whole genome…
Updated Oct 29, 2026
HealthData.Gov
Quickly identifying segments of a nucleic acid sequence that may be of vector origin.
Updated Oct 29, 2026
HealthData.Gov
Supports finding human phenotype/genotype relationships with queries by phenotype, chromosome location, gene, and SNP identifiers. Currently includes information from dbGaP, the National Human Genome Research Institute…
Updated Oct 29, 2026
HealthData.Gov
Database of Genotype and Phenotype (dbGaP) was developed to archive and distribute the data and results from studies that have investigated the interaction of genotype and phenotype in Humans.
Updated Oct 29, 2026
HealthData.Gov
The Consensus CDS (CCDS) project is a collaborative effort to identify a core set of human and mouse protein coding regions that are consistently annotated and of high quality. The long term goal is to support…
Updated Oct 29, 2026
HealthData.Gov
The BioProject database links to data that have been or will be deposited into archival databases maintained at members of the International Nucleotide Sequence Database Consortium (INSDC, which comprises the DNA…
Updated Oct 29, 2026
HealthData.Gov
A graphical analysis tool that finds all open reading frames in a user's sequence or in a sequence already in the database.
Updated Oct 29, 2026
HealthData.Gov
MedGen is NCBI's portal to information about conditions and phenotypes related to Medical Genetics. Terms from the NIH Genetic Testing Registry (GTR), UMLS, HPO, Orphanet, ClinVar and other sources are aggregated into…
Updated Oct 29, 2026
HealthData.Gov
The PopSet database is a collection of related DNA sequences derived from population, phylogenetic, mutation and ecosystem studies that have been submitted to GenBank.
Updated Oct 29, 2026
HealthData.Gov
ClinVar aggregates information about genomic variation and its relationship to human health.
Updated Oct 29, 2026
HealthData.Gov
An automated analytical system for producing organized views of the transcriptome from a growing number of organisms. UniGene was retired in July 2019; however, you will continue to be able to access archived data.
Updated Oct 29, 2026
HealthData.Gov
The Sequence Read Archive (SRA) stores sequencing data from the next generation of sequencing platforms including Roche 454 GS System®, Illumina Genome Analyzer®, Life Technologies AB SOLiD System®, Helicos Biosciences…
Updated Oct 29, 2026
