ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden is a dataset published in medRxiv (2022). On theSindex it has a DataRank of 0.120, placing it in the top 71.5% of the data-sharing corpus. It has been cited 1 time, with 1 citing works in its 1-hop citation network.
Ranks in the top 71% for downstream scientific impact
DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?
FAIR checklist signals are shown for context only and do not affect DataRank scoring.
We only score data papers we can read in full — never from an abstract alone.
Base Score Contribution
0.104
From this paper's citation signal
Citation Network Contribution
0.0159
From 1 citing papers with measurable signal
Ranked by each citer's contribution to N(p) — log1p(Cq) divided by its reference count — out of 1 citer.
National Institutes of Health
Grant: 5P01AI138962-02
Inherited T cell defects: Diagnosis, Mechanisms and Treatments
National Science Foundation
Grant: 1752814
Graduate Research Fellowship Program (GRFP)
National Institutes of Health
Grant: 3U19HD077627-04S1
Sequencing of Newborn Blood Spot DNA to Improve and Expand Newborn Screening
National Institutes of Health
Grant: 5U41HG007346-03
Center for Critical Assessment of Genome Interpretation
National Science Foundation
Grant: 2109912
NSF Postdoctoral Fellowship in Biology FY 2021: Are variants under selection for disease resistance predictive of disease susceptibility across taxa?
National Institutes of Health
Grant: 5U24HG007346-08
Center for Critical Assessment of Genome Interpretation
Fields of Study
Keywords
Sustainable Development Goals