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Closing the gaps, and improving somatic structural variant analysis and benchmarking using CHM13-T2T

Genome Research(2025)10.1101/gr.279352.124Source: DataRank Database

Closing the gaps, and improving somatic structural variant analysis and benchmarking using CHM13-T2T is a research paper published in Genome Research (2025). On theSindex it has a DataRank of 0. It has been cited 7 times.

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0DataRank · unranked

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Open Access7 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (5 grants)OA: bronzeTopics (20)IDs (PubMed, PMC)

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Findable (1/2)

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Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (7)

Jeremy Fan,Kieran O’Neill ORCID,Erin Pleasance ORCID,Vanessa Porter ORCID,Steven J.M. Jones ORCID

Live enrichment

PubMed:40097200 PMC:PMC12047239

NIH

Grant: UM1DA058229

NIH

Grant: 1UG3NS132105-01

NIH

Grant: 1U01HG011758-01

NHGRI NIH HHS

Grant: U01 HG011758

NINDS NIH HHS

Grant: UG3 NS132105

bronze

publisherhttp://genome.cshlp.org/content/early/2025/03/17/gr.279352.124.full.pdf

publisherhttps://syndication.highwire.org/content/doi/10.1101/gr.279352.124

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC12047239/

Europe_PMChttps://europepmc.org/articles/PMC12047239

Europe_PMChttps://europepmc.org/articles/PMC12047239?pdf=render

Fields of Study

HumansBenchmarkingGenome, HumanGenomic Structural VariationHigh-Throughput Nucleotide SequencingNeoplasmsCell Line, TumorSequence Analysis, DNAMolecular Sequence AnnotationComputational Biology

MeSH Terms

Cell Line, TumorHumansNeoplasmsSequence Analysis, DNAComputational BiologyGenome, HumanBenchmarkingGenomic Structural VariationMolecular Sequence AnnotationHigh-Throughput Nucleotide Sequencing