Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel is a dataset published in Nature Communications (2015). On theSindex it has a DataRank of 6.7, placing it in the top 2.8% of the data-sharing corpus. It has been cited 386 times, with 100 citing works in its 1-hop citation network. Its calibrated FAIR score is 54/100.
Ranks in the top 3% 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.
Full FAIR picture · advisory
This score predates the current agent — it came from the earlier rubric, which blended repository metadata into the number and asked the model for a rating rather than an evidenced verdict. Re-evaluate the paper to score it against the current standards-anchored criteria, where every verdict is backed by a quote from the full text.
DOI present
datacite=6, pmcid=True, pmid=True
no OpenAlex id
The paper provides a DOI and mentions accession codes (EGAS, EGAD) but does not describe machine-readable metadata such as structured data dictionaries or formal metadata schemas.
files/OA location present but not flagged OA
41 OA location(s)
The paper states that UK10K haplotypes are available from the European Genome-phenome Archive under managed access and provides a URL for data access, but does not detail a fully automated or standardized access protocol.
linked_datasets=0, datacite=6
accessions=0, trials=0
The paper uses standard formats like VCF and BAM and references common tools (e.g., SAMtools, BWA), but does not explicitly state use of standard ontologies or persistent identifiers for variables.
no license
downloads=0
no version chain
is_dataset
The paper includes a data-availability statement with an EGA accession, a Creative Commons license (CC BY 4.0), and describes methods for reproducibility, but lacks a clear statement on code availability or a formal reproducibility checklist.
Calibrated FAIR score — a parallel quality metric, independent of the DataRank citation score. See the full evaluation →
Base Score Contribution
0.894
From this paper's citation signal
Citation Network Contribution
5.8
From 100 citing papers with measurable signal
Ranked by each citer's contribution to N(p) — log1p(Cq) divided by its reference count — out of 100 citers.
Wellcome Trust
Grant: 095564
British Heart Foundation
Grant: RG/10/13/28570
Wellcome Trust
Grant: 098497
Medical Research Council
Grant: MC_PC_15018
Medical Research Council
Grant: MC_UU_12013/3
Causal analyses, statistical efficiency and phenotypic precision through study design: Genotype based sampling
Medical Research Council
Grant: MR/L010305/1
National Institute for Health Research (NIHR)
Grant: NF-SI-0510-10268
Wellcome Trust
Grant: WT091310
Medical Research Council
Grant: MC_UU_12012/5
Wellcome Trust
Grant: WT098051
Wellcome Trust
Grant: 098498
Medical Research Council
Grant: G0800509
National Institute for Health Research (NIHR)
Grant: NF-SI-0508-10198
National Institute for Health Research (NIHR)
Grant: NF-SI-0513-10109
British Heart Foundation
Grant: PG/13/66/30442
British Heart Foundation
Grant: RG/10/17/28553
Wellcome Trust
Grant: 091551
Wellcome Trust
Grant: 100140
European Research Council
Grant: 617306
ADVANCED STATISTICAL METHODS FOR HIGH-DIMENSIONAL GENETIC STUDIES
Medical Research Council
Grant: MC_UU_12015/1
National Institute for Health Research (NIHR)
Grant: NF-SI-0513-10008
Economic and Social Research Council
Grant: ES/M001660/1
Medical Research Council
Grant: MC_UU_12013/1
Medical Research Council
Grant: MC_UU_12013/4
Wellcome Trust
Grant: 095515
Wellcome Trust
Grant: 096599
Wellcome Trust
Grant: 102215
National Institute for Health Research (NIHR)
Grant: NIHR-RP-R3-12-013
Wellcome Trust
Grant: 100574
Wellcome Trust
Grant: 104036/Z/14/Z
Medical Research Council
Grant: MC_UU_12012/5/B
National Institute for Health Research (NIHR)
Grant: NF-SI-0507-10380
National Institute for Health Research (NIHR)
Grant: NF-SI-0514-10027
National Institute for Health Research (NIHR)
Grant: NF-SI-0514-10176
European Commission
Grant: 282510
A BLUEPRINT of Haematopoietic Epigenomes
Canadian Institutes of Health Research
Grant: unidentified
unidentified
European Commission
Grant: 257082
Epigenetics towards systems biology
Wellcome Trust
Grant: 091310
10,000 UK genome sequences: accessing the role of rare genetic variants in health and disease.
Wellcome Trust
Grant: 098051
Wellcome Trust Sanger Institute - generic account for deposition of all core- funded research papers
CIHR
National Institute for Health Research (NIHR)
CIHR
Department of Health
FWCI
27.46
Citation Percentile
1.0%
Citation Trend
Fields of Study
MeSH Terms
Keywords