A sequence of SVA retrotransposon insertions in ASIP shaped human pigmentation is a research paper published in Nature Genetics (2024). On theSindex it has a DataRank of 0.434. It has been cited 17 times.
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DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?
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Base Score Contribution
0.434
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 →U.S. Department of Health & Human Services | National Institutes of Health
Grant: T32 HG002295
U.S. Department of Health & Human Services | National Institutes of Health
Grant: F32 HL160061
U.S. Department of Health & Human Services | National Institutes of Health
Grant: K25 HL150334
U.S. Department of Health & Human Services | National Institutes of Health
Grant: R01 HG006855
U.S. Department of Health & Human Services | National Institutes of Health
Grant: DP2 ES030554
U.S. Department of Health & Human Services | National Institutes of Health
Grant: R56 HG012698
U.S. Department of Health & Human Services | National Institutes of Health
Grant: R01 HG013110
National Institutes of Health
Grant: 1K25HL150334-01
Exploring the role of genomic repeats in cardiovascular disease heritability
National Institutes of Health
Grant: 5F32HL160061-02
Exploring the role of genomic copy number variation in cardiovascular disease risk
National Institutes of Health
Grant: 5R01HG013110-02
Leveraging biobank-scale whole-genome sequencing for polygenic risk prediction
National Institutes of Health
Grant: 5R01HG006855-02
Multi-allelic copy number variation of the human genome
National Institutes of Health
Grant: 5T32HG002295-23
Training in Bioinformatics and Integrative Genomics
National Institutes of Health
Grant: 1DP2ES030554-01
Revealing somatic genome alterations and their clinical sequelae: Ultrasensitive computational detection of mosaic structural variants
National Institutes of Health
Grant: 1R56HG012698-01A1
Identifying structural variants influencing human health in population cohorts
Broad Institute
Burroughs Wellcome Fund
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