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Accessible high-throughput single-cell whole-genome sequencing with paired chromatin accessibility

Cell Reports Methods(2023)10.1016/j.crmeth.2023.100625Source: DataRank Database

Accessible high-throughput single-cell whole-genome sequencing with paired chromatin accessibility is a research paper published in Cell Reports Methods (2023). On theSindex it has a DataRank of 0. It has been cited 9 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access9 citations

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Enrichment:Funding (7 grants)Impact (FWCI 1.04)OA: goldTopics (43)IDs (PubMed, PMC, OpenAlex)Annotations (2)

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 (11)

Travis W. Moore,Brendan L. O’Connell ORCID,Ruth V. Nichols ORCID,John Muschler ORCID,Dove Keith ORCID

Live enrichment

PubMed:37918402 PMC:PMC10694488 OpenAlex:https://openalex.org/W4388141144

National Institute of General Medical Sciences

Grant: 5T32GM142619-02

Program in Biomedical Sciences

National Cancer Institute

Grant: R33CA269015

National Cancer Institute

Grant: IMAT R33

NIGMS NIH HHS

Grant: T32 GM142619

NIGMS NIH HHS

Grant: R35 GM147698

National Institutes of Health

Grant: 1R33CA269015-01

Accessible high-throughput single-cell genome sequencing

National Institutes of Health

FWCI

1.04

Citation Percentile

0.8%

Citation Trend

2024

2025

2026

goldLicense: cc-by-nc-nd

journalhttps://doi.org/10.1016/j.crmeth.2023.100625

publisherhttps://doi.org/10.1016/j.crmeth.2023.100625

publisherhttps://api.elsevier.com/content/article/PII:S2667237523002898?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S2667237523002898?httpAccept=text/plain

repositoryhttps://pubmed.ncbi.nlm.nih.gov/37918402

Fields of Study

Cancer Genomics and DiagnosticsSingle-cell and spatial transcriptomicsGenomic variations and chromosomal abnormalities0206 medical engineering02 engineering and technology

MeSH Terms

ChromatinNucleosomesGenomeSequence Analysis, DNAHigh-Throughput Nucleotide Sequencing

Keywords

WorkflowThroughputComputational biologyComputer scienceGenomeDNA sequencingMultiplexingGenomicsChromatinSample (material)BiologyGeneticsDNAGeneDatabaseChemistryTelecommunicationsCancer BiologyChromatin AccessibilitySingle-cell GenomicsCopy-number AlterationsCp: BiotechnologyCp: GeneticsScienceQHigh-Throughput Nucleotide SequencingQD415-436Sequence Analysis, DNABiochemistryNucleosomesReportTP248.13-248.65Biotechnology