SPARC/dbGaP Quick-Reference

Under the NIH Genomic Data Sharing (GDS) Policy, read-level human genomic data must be deposited in a controlled-access repository such as dbGaP. If data does not require controlled access, it can be deposited in SPARC. Responsibility for regulatory compliance remains with the data submitter and Principal Investigator.

This information is provided for general demonstration purposes and is not a substitute for regulatory guidance. Ultimate responsibility for compliance with all applicable mandates — including the NIH Genomic Data Sharing Policy — rests solely with the investigator and Principal Investigator.


Table 1. SPARC and dbGaP Repositories at a Glance

SPARC — Open-access repositorydbGaP — Controlled-access repository
Pennsieve / sparc.science
Non-identifying derived data, metadata, code, protocols
NIH GDS Policy
Human read-level, alignment, variant, and phenotype data

Table 2. Deposit in SPARC

Open-access · Derived, processed, and non-identifying data

Data categoryExamples / contentTypical files / extensions
Derived / processed transcriptomics (bulk RNA-seq)Gene expression summaries (non-identifying)counts.tsv / .csv
tpm.tsv / .csv
DEG_results.tsv / .csv
GSEA / GO / KEGG_results.tsv / .csv
Derived / processed single-cell & single-nucleus RNA-seqCell × gene matrices, cell-type labels, marker genesmatrix.mtx(.gz)
features.tsv(.gz)
barcodes.tsv(.gz)
*_feature_bc_matrix.h5
cell_annotations.csv
markers.csv
Derived ATAC / accessibility outputsPeaks and summarized accessibilitypeaks.bed
peak_matrix.mtx / .h5
motif_enrichment.tsv
summary plots (.pdf / .png)
Visium spatial (Space Ranger summaries)Spot × gene matrices + spatial metadatafiltered_feature_bc_matrix/*
raw_feature_bc_matrix/*
spatial/scalefactors_json.json
tissue_positions*.csv
.cloupe
web_summary.html
Xenium summariesCell × gene matrices, segmentations, QC, de-identified imagescell_feature_matrix/* (MEX/H5/Zarr)
cell_boundaries.parquet
nucleus_boundaries.parquet
QC html / csv
de-ID images (PNG / TIFF / OME-TIFF / JP2)
QC reports (no reads)Pipeline summaries and metricsweb_summary.html
metrics_summary.csv
multiqc_report.html
QC reports (.pdf)
Analysis code & workflowsReproducibility artifacts.R / .py / .ipynb
Dockerfile
environment.yml / requirements.txt
workflow configs (.yaml / .json)
Non-genomic modalities (de-identified)Imaging, histology, microscopy; physiology / ephysSee SPARC accepted file formats
DocumentationMethods, protocols, README, crosswalkREADME.md
protocol docs (.docx / .pdf)
SDS metadata files

Table 3. Deposit in dbGaP

Controlled-access · Human read-level, alignment, variant, and phenotype data

Data categoryExamples / contentTypical files / extensions
Read-level sequencingRaw reads + base quality scores*.fastq / .fq / .fastq.gz / .fq.gz
BCL run folders
Alignments / near-rawAligned or unaligned reads*.bam + index (.bai / .csi)
*.cram + index (.crai)
uBAM (unaligned .bam)
VariantsGenotype / variant calls*.vcf / .vcf.gz + index (.tbi / .csi)
*.g.vcf / .g.vcf.gz + index (.tbi / .csi)
Nanopore / PacBio rawLong-read raw signal or subreadsNanopore: .fast5 / .pod5
PacBio: subreads.bam / *.bax.h5
Participant-level phenotypes & consentsIndividual-level clinical / phenotype data + consent termsConsent documents (.pdf / .docx / .xlsx)
⚠️ Note: This table is a non-exhaustive quick-reference. Companion and index files (.bai, .csi, .tbi, .crai) that enable interpretation or reconstruction of underlying controlled-access genomic data are also subject to controlled-access deposition requirements. For ambiguous cases, consult your NIH Genomic Program Administrator (GPA) before depositing.



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