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
Top 12%
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