bioRxivCell BiologyPreprint
The HuBMAP Framework for Advancing Data FAIRness
Stephen A. FisheriD, Josef HardiiD, Richard S. MorganiD, Erik C. NordgreniD, Peter M. Kant, Brendan John HonickiD, Jean G. RosarioiD, Martin J. O’ConnoriD, Philip D. BloodiD, HuBMAP DCWG Members, Jonathan C. SilversteiniD, Mark A. MuseniD
Abstract
Since publication of the FAIR Guiding Principles in 2016, the scientific community has increasingly sought to make experimental data findable, accessible, interoperable, and reusable. Operationalizing the FAIR principles in routine scientific workflows remains challenging without a standardized, workable infrastructure. With over 10,000 datasets from over 40 institutions, spanning more than 50 diverse assay types ranging from single-cell sequencing technologies to 2D and 3D spatial omics, the U.S. National Institutes of Health (NIH) Human Bio-Molecular Atlas Program (HuBMAP) consortium has been ideally situated to create a FAIR ecosystem. With the goal of achieving data "FAIRness," HuBMAP developed and implemented well-defined, community-endorsed metadata reporting standards across the research lifecycle. These reporting standards include detailed schemas, harmonized across a multitude of assays, that define the metadata associated with a dataset and the organization of the corresponding data files. These standards ensure documentation of the data collection process, of the data themselves, and of the manner in which the data are packaged for sharing, while remaining compliant with the Health Insurance Portability and Accountability Act (HIPAA). The use of these reporting standards, in tandem with technology to foster adherence, allows HuBMAP to fulfill its goal of generating FAIR data for open dissemination through its Data Portal and Human Reference Atlas. The procedures and simple workflow adopted by HuBMAP investigators serve as a model for other scientific communities aiming to maximize the value of varied datasets addressing a shared research question. The HuBMAP end-to-end, metadata-centered workflow has been replicated and enhanced by the NIH Cellular Senescence Network (SenNet) consortium and is readily available through open-source technology for others to utilize.
- assay: spatial transcriptomics
- assay: bulk RNA-seq
- assay: ATAC-seq
- assay: Hi-C
- research focus: database / resource
- research focus: benchmarking
- research focus: cell type annotation
- research focus: clustering
- approach: experimental assay
- Citations
- 1
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