🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge
Demo corpus. Scores are computed on a select set of biomedical paper/datasets and may be inaccurate for papers outside this corpus — DataRank relies on network effects that improve with scale. We aim to expand this into a fully open resource pending additional funding.

PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

Genome Research(2007)10.1101/gr.6861907Source: DataRank Database
Top 12%
18.5DataRank
18.5Top 12%
Open Access
1896 citations · base score 7.5
datarank_citation_only_1hop_v4Methodology
Data sources & pipeline
Pipeline:CrossRefSciBERTdoi-metadataOpenAlexDataRank
Enrichment:Pending
FAIR ChecklistContext only (not used in score)
FFindable
Has DOI
AAccessible
Open Access
IInteroperable
RReusable

FAIR checklist signals are shown for context only and do not affect DataRank scoring.

DataRank Breakdown

Base Component 6%Network Component 94%

Base Score Contribution

1.1

From this paper's citation signal

Citation Network Contribution

17.4

From 175 citing papers with measurable signal

Learn more about DataRank methodology →

Authors (10)

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