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 0.633. It has been cited 67 times.
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Base Score Contribution
0.633
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 →NIH HHS
Grant: R24 OD011883
NICHD NIH HHS
Grant: R01 HD103805
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
FWCI
4.10
Citation Percentile
1.0%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals
Additional file 1 of PDIVAS: Pathogenicity predictor for Deep-Intronic Variants causing Aberrant Splicing
Additional file 1 of PDIVAS: Pathogenicity predictor for Deep-Intronic Variants causing Aberrant Splicing
Additional file 1 of SpliceAI-visual: a free online tool to improve SpliceAI splicing variant interpretation
Additional file 1 of SpliceAI-visual: a free online tool to improve SpliceAI splicing variant interpretation
Squirls | v1 | ingest files
Squirls | v1 | ingest files