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Accurate detection of somatic single-nucleotide variants from bulk RNA-seq data using RNA-MosaicHunter

Nucleic Acids Research(2025)10.1093/nar/gkaf1450Source: DataRank Database

Accurate detection of somatic single-nucleotide variants from bulk RNA-seq data using RNA-MosaicHunter is a research paper published in Nucleic Acids Research (2025). On theSindex it has a DataRank of 0. It has been cited 1 time.

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Open Access1 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (4 grants)Impact (FWCI 1.88)OA: goldTopics (26)IDs (PubMed, PMC, OpenAlex)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (8)

Yuchen Cheng,Jayoung Ku ORCID,Boxun Zhao ORCID,Junseok Park ORCID,Dachan Kim ORCID

Live enrichment

PubMed:41505106 PMC:PMC12781890 OpenAlex:https://openalex.org/W7119885985

National Institutes of Health

Grant: DP2AG072437

National Institutes of Health

Grant: R01AG070921

National Institutes of Health

Grant: R56AG079857

National Institutes of Health

Grant: R01AG088082

FWCI

1.88

Citation Percentile

0.9%

Citation Trend

2026

goldLicense: cc-by

journalhttps://doi.org/10.1093/nar/gkaf1450

publisherhttps://doi.org/10.1093/nar/gkaf1450

publisherhttps://academic.oup.com/nar/article-pdf/54/1/gkaf1450/66308118/gkaf1450.pdf

repositoryhttps://pubmed.ncbi.nlm.nih.gov/41505106

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC12781890/

Fields of Study

Genomics and Rare DiseasesCancer Genomics and DiagnosticsSingle-cell and spatial transcriptomicsHumansPolymorphism, Single NucleotideAlzheimer DiseaseRNA-SeqSoftwareComputational BiologyMutationSequence Analysis, RNA

MeSH Terms

RNA-SeqAlzheimer DiseaseHumansMutationSoftwareSequence Analysis, RNAComputational BiologyPolymorphism, Single Nucleotide

Keywords

Somatic cellGenotypeDNA sequencingProfiling (computer programming)Deep sequencingBenchmarkingGermline mutation