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

TRIO RVEMVS: A Bayesian framework for rare variant association analysis with expectation-maximization variable selection using family trio data

PLoS ONE(2024)10.1371/journal.pone.0314502Source: DataRank Database

TRIO RVEMVS: A Bayesian framework for rare variant association analysis with expectation-maximization variable selection using family trio data is a research paper published in PLoS ONE (2024). On theSindex it has a DataRank of 0.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access0 citations

Download PDF

Cite:

Linked data & code

refsnp

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 (2 grants)Impact (FWCI 0.00)OA: goldTopics (55)IDs (PubMed, PMC, OpenAlex)Annotations (1)SDGs (1)

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)

Matthew D. Koslovsky ORCID,Margaret C. Steiner ORCID,Kusha Mohammadi ORCID,Chenguang Zhang ORCID,Michael D. Swartz ORCID

Live enrichment

PubMed:39630689 PMC:PMC11616829 OpenAlex:https://openalex.org/W4405023775

NIH/NICHD

Grant: R03HD083674

National Institutes of Health

Grant: 5R03HD083674-02

A Novel Trio-based Bayesian Method to Identify Rare Variants for Birth Defects

FWCI

0.00

Citation Percentile

0.2%

goldLicense: cc-by

journalhttps://doi.org/10.1371/journal.pone.0314502

GOLDhttps://doi.org/10.1371/journal.pone.0314502

publisherhttps://doi.org/10.1371/journal.pone.0314502

publisherhttps://dx.plos.org/10.1371/journal.pone.0314502

repositoryhttps://pubmed.ncbi.nlm.nih.gov/39630689

Fields of Study

Genetic Associations and EpidemiologyGenomic variations and chromosomal abnormalitiesCleft Lip and Palate ResearchMedicineComputer Science0301 basic medicine0303 health sciences03 medical and health sciencesHumansBayes TheoremPedigreeGene FrequencyModels, GeneticLinkage DisequilibriumGenetic Predisposition to DiseaseGenetic VariationPolymorphism, Single NucleotideComputer Simulation

MeSH Terms

Bayes TheoremComputer SimulationGene FrequencyHumansModels, GeneticPedigreeGenetic VariationLinkage DisequilibriumGenetic Predisposition to DiseasePolymorphism, Single Nucleotide

Keywords

Minor allele frequencyGeneticsTransmission disequilibrium testSelection (genetic algorithm)PopulationBiologyAllele frequencyAlleleMedicineComputer scienceGeneArtificial intelligenceModels, GeneticScienceQR610Genetic VariationBayes TheoremPolymorphism, Single NucleotideLinkage DisequilibriumPedigreeGene FrequencyHumansGenetic Predisposition to DiseaseComputer SimulationResearch Article

Sustainable Development Goals

SDG 0: Good health and well-being