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Datasets

88 datasets

HealthData.Gov

HHS COVID-19 Monthly Outcome Survey - Wave 07

The Monthly Outcome Survey (MOS) was designed to assess COVID-19 vaccine uptake as well as beliefs, intentions, and behaviors relevant to COVID-19 vaccination at a point in time. The survey fielded on a monthly basis…

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Updated Oct 29, 2026

HealthData.Gov

ProSplign

A utility for computing alignment of proteins to genomic nucleotide sequence based on a variation of the Needleman Wunsch global alignment algorithm and specifically accounts for introns and splice signals.

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Updated Oct 29, 2026

HealthData.Gov

Protein

The Protein database is a collection of sequences from several sources, including translations from annotated coding regions in GenBank, RefSeq and TPA, as well as records from SwissProt, PIR, PRF, and PDB. Protein…

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Updated Oct 29, 2026

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CDTree

CDTree is a stand-alone application for classifying protein sequences and investigating their evolutionary relationships. CDTree can import, analyze and update existing Conserved Domain (CDD) records and hierarchies,…

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Updated Oct 29, 2026

HealthData.Gov

GEO (Gene Expression Omnibus)

GEO (Gene Expression Omnibus) is a public functional genomics data repository supporting MIAME-compliant data submissions. There are also tools provided to help users query and download experiments and curated gene…

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Updated Oct 29, 2026

HealthData.Gov

SNOMED CT

SNOMED CT is one of a suite of designated standards for use in U.S. Federal Government systems for the electronic exchange of clinical health information and is also a required standard in interoperability…

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Updated Oct 29, 2026

HealthData.Gov

Retrovirus Resources

Information about retroviruses and specialized tools for the analysis of retroviral proteins and genomes. The tools on this page aid in the identification, study and analysis of retroviral genomes and proteins. For…

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Updated Oct 29, 2026

HealthData.Gov

Database of Genomic Structural Variation (dbVar)

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,…

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Updated Oct 29, 2026

HealthData.Gov

RxTerms

RxTerms is a drug interface terminology derived from RxNorm for prescription writing or medication history recording (e.g. in e-prescribing systems, PHRs). RxTerms is derived only from the non-proprietary content of…

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Updated Oct 29, 2026

HealthData.Gov

MEDLINE/PubMed Citations

PubMed is a free resource supporting the search and retrieval of biomedical and life sciences literature with the aim of improving health–both globally and personally. The PubMed database contains citations and…

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Updated Oct 29, 2026

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Protein Clusters

A collection of Reference Sequence (RefSeq) proteins, from the complete genomes of prokaryotes, plasmids, and organelles, that have been grouped and annotated based on sequence similarity and protein function.

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Updated Oct 29, 2026

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Database of Genotype and Phenotype (dbGaP)

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.

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Updated Oct 29, 2026

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Conserved Domain Database (CDD)

Conserved Domain Database (CDD) is a protein annotation resource that consists of a collection of well-annotated multiple sequence alignment models for ancient domains and full-length proteins.

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Updated Oct 29, 2026

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OLDMEDLINE Data

The OLDMEDLINE subset in PubMed® represents journal article citations from two print indexes: Cumulated Index Medicus (CIM) and the Current List of Medical Literature (CLML). Created by the National Library of Medicine®…

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Updated Oct 29, 2026

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HomoloGene

System for automated detection of homologs among the annotated genes of several completely sequenced eukaryotic genomes.

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Updated Oct 29, 2026

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Consensus CDS (CCDS)

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…

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Updated Oct 29, 2026

HealthData.Gov

Value Set Authority Center

The VSAC is a repository and authoring tool for public value sets created by external programs. Value sets are lists of codes and corresponding terms, from NLM-hosted standard clinical vocabularies (such as SNOMED CT®,…

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Updated Oct 29, 2026

HealthData.Gov

PubChem

PubChem contains the chemical structures of small organic molecules and information on their biological activities. PubChem includes substance information, compound structures, and bioactivity data in three primary…

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Updated Oct 29, 2026

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RefSeq: NCBI Reference Sequence Database

A comprehensive, integrated, non-redundant, well-annotated set of reference sequences including genomic, transcript, and protein.

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Updated Oct 29, 2026

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Third Party Annotation (TPA) Database

A database that contains sequences built from the existing primary sequence data in GenBank. The sequences and corresponding annotations are experimentally supported and have been published in a peer-reviewed scientific…

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Updated Oct 29, 2026

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