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Rapid Visualisation of Microarray Copy Number Data for the Detection of Structural Variations Linked to a Disease Phenotype

PLoS ONE(2012)10.1371/journal.pone.0043466Source: DataRank Database

Rapid Visualisation of Microarray Copy Number Data for the Detection of Structural Variations Linked to a Disease Phenotype is a research paper published in PLoS ONE (2012). On theSindex it has a DataRank of 0.165. It has been cited 2 times.

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0.165DataRank · unranked

Scored on demand from live citation data

2 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (2 grants)Impact (FWCI 0.38)OA: goldTopics (50)IDs (PubMed, PMC, OpenAlex)Annotations (1)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (0/2)

Interoperable (0/2)

Reusable (0/3)

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DataRank Breakdown

Base Score 100%Citation Network 0%

Base Score Contribution

0.165

From this paper's citation signal

Citation Network Contribution

Citation network not refreshed for this result

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Authors (11)

Christine P. Diggle,Kamron Khan,Chris Inglehearn,Martin McKibbin ORCID,David T. Bonthron ORCID

Live enrichment

PubMed:22912880 PMC:PMC3422275 OpenAlex:https://openalex.org/W2082810381

Engineering and Physical Sciences Research Council

Grant: EP/I000623/1

Cancer Research UK

Grant: 600130

FWCI

0.38

Citation Percentile

0.7%

Citation Trend

2013

2014

goldLicense: cc-by

journalhttps://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0043466&type=printable

publisherhttps://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0043466&type=printable

journalhttps://doi.org/10.1371/journal.pone.0043466

repositoryhttps://pubmed.ncbi.nlm.nih.gov/22912880

repositoryhttp://eprints.whiterose.ac.uk/89196/1/Rapid%20visualisation%20of%20microarray%20copy%20number%20data%20for%20the%20detection%20of%20structural%20variations%20linked%20to%20a%20disease%20phenotype..pdf

Fields of Study

Genomic variations and chromosomal abnormalitiesPrenatal Screening and DiagnosticsGenomics and Rare DiseasesAniridiaChromosome AberrationsChromosome MappingDNA Copy Number VariationsFamily HealthFemaleGenetic Association StudiesGenetic Predisposition to DiseaseGenome, HumanHumansLoss of HeterozygosityMaleOligonucleotide Array Sequence AnalysisPedigreePhenotypePolymorphism, Single NucleotideReproducibility of ResultsSoftware

MeSH Terms

Chromosome AberrationsChromosome MappingFamily HealthFemaleHumansMalePedigreePhenotypeSoftwareReproducibility of ResultsAniridiaGenome, HumanLoss of HeterozygosityGenetic Predisposition to DiseaseOligonucleotide Array Sequence AnalysisPolymorphism, Single NucleotideGenetic Association StudiesDNA Copy Number Variations

Keywords

Copy-number variationBiologyCopy number analysisStructural variationGeneticsGenomePhenotypeOligonucleotideComparative genomic hybridizationComputational biologyGene

Rapid Visualisation of Microarray Copy Number Data for the Detection of Structural Variations Linked to a Disease Phenotype

FAIR Checklist

DataRank Breakdown

Authors (11)

Funding (2 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)