De novo assembly of 64 haplotype-resolved human genomes of diverse ancestry and integrated analysis of structural variation is a dataset published in bioRxiv (Cold Spring Harbor Laboratory) (2020). On theSindex it has a DataRank of 0.322, placing it in the top 52.8% of the data-sharing corpus. It has been cited 5 times, with 3 citing works in its 1-hop citation network.
Ranks in the top 53% for downstream scientific impact
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.
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Base Score Contribution
0.269
From this paper's citation signal
Citation Network Contribution
0.0537
From 3 citing papers with measurable signal
Ranked by each citer's contribution to N(p) — log1p(Cq) divided by its reference count — out of 3 citers.
Wellcome Trust
Grant: 104947
The International Genome Sample Resource.
National Institutes of Health
Grant: 5U24HG007497-07
Identifying and Characterizing the Full Spectrum of Haplotype-resolved Structural Variation in Human Genomes
National Institutes of Health
Grant: 5R01HD081256-10
Clinical Diagnostic Sequencing of Structural Variation
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: 1R15HG009565-01
A Computational Framework for Scalable Epistasis Analysis on High-Dimensional Genomic Data.
Wellcome Trust
Grant: 085532
Trace Archive and 1KG DCC.
National Institutes of Health
Grant: 5R35GM138212-03
Structural variation analysis with and without a reference genome
European Commission
Grant: 716290
Finding the genetic causes of contagious metastases under the sea
National Institutes of Health
Grant: 5R01HG002385-15
Sequence and Assembly of Segmental Duplications
National Institutes of Health
Grant: 3UM1HG008901-03S1
New York Center for Collaborative Research in Common Disease Genomics
National Institutes of Health
Grant: 1R01HG007068-01A1
Discovery and analysis of structural variation in whole genome sequences
National Institutes of Health
Grant: 5K99HG011041-02
The fitness effects of de novo structural variants
National Institutes of Health
Grant: 1OT3HL147154-01
NHLBI Data Stage Coordinating Center
European Commission
Grant: 773026
Relationship of Somatic Structural Variation Mosaicism to Aging and Disease Phenotypes
National Institutes of Health
Grant: 1U01HG010973-01
Representing structural haplotypes and complex genetic variation in pan-genome graphs
National Institutes of Health
Grant: 5R01HG002898-03
Natural genetic variation in the human genome
Fields of Study
Keywords
HGSVC2 project code contributions
HGSVC2 project code contributions
HGSVC2 project code contributions
Multiple sequence alignments of full-length L1 elements with evidence of retrotransposition activity.
Multiple sequence alignments of full-length L1 elements with evidence of retrotransposition activity.