The NeuroHIV Data Ecosystem is part of the broader network of NIH-supported data repositories that promote open science, data harmonization, and responsible data sharing. As researchers engage with our platform—whether accessing or contributing data—we encourage the use of complementary NIH resources to enhance data interoperability and discoverability.
Below, you’ll find links to key NIH-supported repositories and reference materials that can be used alongside the NeuroHIV Data Ecosystem. These resources provide additional context, tools, and infrastructure to support your data management and sharing efforts in alignment with NIH policies and best practices.
NIMH Data Archive (NDA)
The National Institute of Mental Health Data Archive (NDA) makes available human subjects data collected from hundreds of research projects across many scientific domains. NDA provides infrastructure for sharing research data, tools, methods, and analyses enabling collaborative science and discovery. De-identified human subjects data, harmonized to a common standard, are available to qualified researchers. Summary data are available to all.
dbGAP
The database of Genotypes and Phenotypes (dbGaP) was developed to archive and distribute the data and results from studies that have investigated the interaction of genotype and phenotype in Humans.
GEO
GEO is a public functional genomics data repository that archives open-access array- and sequence-based datasets. Tools are provided to help users query and download experiments and curated gene expression profiles.
GenBank
GenBank is the NIH genetic sequence database, an annotated collection of publicly available DNA sequences. GenBank captures, preserves, and presents comprehensive nucleotide sequence information and annotations from around the world and connects these data, where applicable, to associated scientific publications and the biological specimens from which the data were derived to preserve the scientific record and enable broad sharing of such data. GenBank preserves nucleotide sequence data to support science necessary for the study of human health, food safety and security, and biodiversity, and other important domains.
MassIVE
MassIVE is a community resource for Computational Mass Spectrometry to promote the global, free exchange of mass spectrometry data.
Sequence Read Archive (SRA)
Sequence Read Archive (SRA) data, available through multiple cloud providers and NCBI servers, is a broad scope publicly available repository of high throughput sequencing data. The archive accepts data from all branches of life as well as metagenomic and environmental surveys. SRA stores raw sequencing data and alignment information to enhance reproducibility and facilitate new discoveries through data analysis.