Analysis workflow to assess de novo genetic variants from human whole-exome sequencing is a research paper published in STAR Protocols (2021). On theSindex it has a DataRank of 0.416. It has been cited 15 times.
Scored on demand from live citation data
Linked data & code
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
0.416
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 →National Institutes of Health
Grant: R00HL143036-02
National Institutes of Health
Grant: T32GM136651
National Institutes of Health
Grant: R01 NS111029-01A1
National Institutes of Health
Grant: R01 NS109358
National Institutes of Health
Grant: K12 228168
American Heart Association
Grant: K99HL143036
American Heart Association
Grant: 19PRE34380842
NHLBI NIH HHS
Grant: R00 HL143036
NCATS NIH HHS
Grant: UL1 TR001863
National Institutes of Health
Grant: 1R01NS111029-01A1
Human genetics and molecular mechanisms of congenital hydrocephalus
National Institutes of Health
Grant: 7R01NS109358-05
Modulation of Choroid Plexus Immuno-secretory Function to Restore Cerebrospinal Fluid Homeostasis in Hydrocephalus
National Institutes of Health
Grant: 1K99HL143036-01A1
Integrative Genomic Analysis of Congenital Heart Disease
National Institutes of Health
Grant: 3T32GM136651-02S2
Medical Scientist Training Program
Rudi Schulte Research Institute
FWCI
1.83
Citation Percentile
0.9%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals