A harmonized public resource of deeply sequenced diverse human genomes is a dataset published in bioRxiv (Cold Spring Harbor Laboratory) (2023). On theSindex it has a DataRank of 1.6, placing it in the top 12.7% of the data-sharing corpus. It has been cited 48 times, with 40 citing works in its 1-hop citation network.
Ranks in the top 13% 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
0.584
From this paper's citation signal
Citation Network Contribution
1.1
From 32 citing papers with measurable signal
Ranked by each citer's contribution to N(p) — log1p(Cq) divided by its reference count — out of 40 citers.
National Institutes of Health
Grant: 1R01DE031261-01
Integration of polygenic risk and facial morphometrics to decipher the genetic susceptibility of orofacial clefting
National Institutes of Health
Grant: 1R01MH115957-01A1
Scalable tool and comprehensive maps to interpret structural variation across the neuropsychiatric spectrum
National Institutes of Health
Grant: 5R37MH107649-07
Statistical methods to localize disease heritability and identify biological mechanisms
National Institutes of Health
Grant: 4R00MH117229-03
Generalizing polygenic risk prediction methods across populations for insights into psychiatric disease
Novo Nordisk Foundation
Grant: unidentified
unidentified
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