Initial sequencing and comparative analysis of the mouse genome
Initial sequencing and comparative analysis of the mouse genome is a dataset published in Nature (2002). On theSindex it has a DataRank of 16.2, placing it in the top 10.3% of the data-sharing corpus. It has been cited 7,236 times, with 142 citing works in its 1-hop citation network. Its calibrated FAIR score is 65/100.
Abstract
The sequence of the mouse genome is a key informational tool for understanding the contents of the human genome and a key experimental tool for biomedical research. Here, we report the results of an international collaboration to produce a high-quality draft sequence of the mouse genome. We also present an initial comparative analysis of the mouse and human genomes, describing some of the insights that can be gleaned from the two sequences. We discuss topics including the analysis of the evolutionary forces shaping the size, structure and sequence of the genomes; the conservation of large-scale synteny across most of the genomes; the much lower extent of sequence orthology covering less than half of the genomes; the proportions of the genomes under selection; the number of protein-coding genes; the expansion of gene families related to reproduction and immunity; the evolution of proteins; and the identification of intraspecies polymorphism.
›Data sources & pipeline
FAIR Checklist
Context only (not used in score)- Has DOI
- Open Access
- 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
14.9
From 142 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.
- Initial sequencing and analysis of the human genomeNature200124,542 citationsDataRank 17.1Top 10%
- An integrated encyclopedia of DNA elements in the human genomeNature201219,311 citationsDataRank 23.8Top 3%
- tRNAscan-SE: A Program for Improved Detection of Transfer RNA Genes in Genomic SequenceNucleic Acids Research199715,868 citationsDataRank 1.5
- The Sequence of the Human GenomeScience200113,648 citationsDataRank 18.7Top 7%
- Mutations of the BRAF gene in human cancerNature200210,637 citationsDataRank 1.4
Why this DataRank?
DataRank blends this paper's own citation count with the influence of the papers that cite it. Here, roughly 8% comes from its base citations and 92% from the citation network (142 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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