Pilot corpus: NIH-funded biomedical datasets. Any DOI can be scored on demand — network effects sharpen as coverage grows.

Deep phenotyping: symptom annotation made simple with SAMS

Nucleic Acids Research(2022)10.1093/nar/gkac329Source: DataRank Database

Deep phenotyping: symptom annotation made simple with SAMS is a research paper published in Nucleic Acids Research (2022). On theSindex it has a DataRank of 0. It has been cited 14 times.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access14 citations

Download PDF

Cite:

DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?

›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (6 grants)OA: goldTopics (24)IDs (PubMed, PMC)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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

Run a calibrated FAIR evaluation for this paper →

We only score data papers we can read in full — never from an abstract alone.

Authors (6)

Sebastian Proft ORCID,Evelyn Seelow ORCID,Tobias Schalau ORCID,Peter N. Robinson ORCID,Dominik Seelow ORCID

Live enrichment

PubMed:35524573 PMC:PMC9252818

NIH NHGRI

Grant: RM1HG010860

Deutsche Forschungsgemeinschaft

Grant: FOR2841 TP05

Deutsche Forschungsgemeinschaft

Grant: TP09

NIH HHS

Grant: R24 OD011883

National Institutes of Health

Grant: 5RM1HG010860-03

A phenomics-first resource for interpretation of variants

Deutsche Forschungsgemeinschaft

Grant: unidentified

unidentified

goldLicense: cc-by

publisherhttps://academic.oup.com/nar/article-pdf/50/W1/W677/44379695/gkac329.pdf

repositoryhttps://mouseion.jax.org/stfb2022/123

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/9252818

repositoryhttps://refubium.fu-berlin.de/handle/fub188/38553

repositoryhttps://doi.org/10.17169/refubium-38269

MeSH Terms

HumansGenomicsPhenotypeMutationSoftwareDatabases, GeneticChild

Keywords

JGMLife Sciences610600GenomicsHuman Phenotype Ontology (HPO)Deep phenotypingPhenotypeWeb Server IssueDatabases, GeneticMutationMedicine and Health SciencesHumansChildSoftwareSymptom Annotation Made Simple (SAMS)600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit