Interpretable prioritization of splice variants in diagnostic next-generation sequencing is a research paper published in The American Journal of Human Genetics (2021). On theSindex it has a DataRank of 0.425. It has been cited 16 times.
Scored on demand from live citation data
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
0.425
From this paper's citation signal
Citation Network Contribution
0
Citation network not refreshed for this result
This paper's DataRank is currently driven only by its base citation score. Citation network data was not refreshed for this result.
Learn more about DataRank methodology →NHGRI NIH HHS
Grant: U24 HG011449
NICHD NIH HHS
Grant: R01 HD103805
NIH HHS
Grant: R24 OD011883
National Institutes of Health
Grant: 1R01HD103805-01
Increasing the Yield and Utility of Pediatric Genomic Medicine with Exomiser
European Commission
Grant: 779257
Solving the unsolved Rare Diseases
National Institutes of Health
Grant: 2R24OD011883-05A1
The Monarch Initiative: Linking Diseases to Model Organism Resources
Fields of Study
Keywords