A haplotype map of the human genome
A haplotype map of the human genome is a dataset published in Nature (2005). On theSindex it has a DataRank of 29.2, placing it in the top 0.8% of the data-sharing corpus. It has been cited 5,917 times, with 200 citing works in its 1-hop citation network. Its calibrated FAIR score is 78/100.
Abstract
Inherited genetic variation has a critical but as yet largely uncharacterized role in human disease. Here we report a public database of common variation in the human genome: more than one million single nucleotide polymorphisms (SNPs) for which accurate and complete genotypes have been obtained in 269 DNA samples from four populations, including ten 500-kilobase regions in which essentially all information about common DNA variation has been extracted. These data document the generality of recombination hotspots, a block-like structure of linkage disequilibrium and low haplotype diversity, leading to substantial correlations of SNPs with many of their neighbours. We show how the HapMap resource can guide the design and analysis of genetic association studies, shed light on structural variation and recombination, and identify loci that may have been subject to natural selection during human evolution.
›Data sources & pipeline
FAIR Checklist
Context only (not used in score)- Has DOI
- Indexed in repositories
- Open Access
- DataCite relations
- Linked datasets
- Dataset classification
FAIR checklist signals are shown for context only and do not affect DataRank scoring.
Calibrated FAIR score — a parallel quality metric, independent of the DataRank citation score. See the full evaluation →
DataRank Breakdown
Base Score Contribution
1.3
From this paper's citation signal
Citation Network Contribution
27.9
From 200 citing papers with measurable signal
Top 5 citers driving the network score
Ranked by citation count — the same ordering the engine uses when summing log1p(Cq) over citers.
- The Sequence of the Human GenomeScience200113,648 citationsDataRank 18.7Top 7%
- Principal components analysis corrects for stratification in genome-wide association studiesNature Genetics200610,642 citationsDataRank 1.4
- A map of human genome variation from population-scale sequencingNature20108,067 citationsDataRank 32.4Top 1%
- Initial sequencing and comparative analysis of the mouse genomeNature20027,236 citationsDataRank 16.2Top 10%
- Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot projectNature20075,248 citationsDataRank 15.6Top 12%
Why this DataRank?
DataRank blends this paper's own citation count with the influence of the papers that cite it. Here, roughly 4% comes from its base citations and 96% from the citation network (200 citing papers contributed measurable signal).
- Base score B(p)
- log1p(citation_count) — grows sub-linearly, so a paper with 1,000 citations is not 10× a paper with 100.
- Network N(p)
- Σ over citers of log1p(Cq) ÷ max(outdegreeq, 1). Being cited by a highly-cited paper with few references counts most.
- Damping factor d = 0.85
- DataRank = (1−d)·B(p) + d·N(p) — the two cards above are each already multiplied by their share.
- Self-citations excluded
- Citers sharing any OpenAlex author ID with this paper are filtered out before the network sum.
Citers are pulled from OpenAlex sorted by cited_by_count:descand capped per paper, so when the cap binds we keep the highest-signal references and the score is reproducible across reruns.
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