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de novo variant calling identifies cancer mutation signatures in the 1000 Genomes Project

Human Mutation(2022)10.1002/humu.24455Source: DataRank Database

de novo variant calling identifies cancer mutation signatures in the 1000 Genomes Project is a research paper published in Human Mutation (2022). On theSindex it has a DataRank of 0. It has been cited 17 times.

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Open Access17 citations

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Enrichment:Funding (5 grants)OA: hybridTopics (18)IDs (PubMed, PMC)Annotations (1)SDGs (1)

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Authors (17)

Pankaj Vats ORCID,Elyn Fritz‐Waters,Stephanie Sarkar,Eleanor I. Sams,Evin M. Padhi ORCID

Live enrichment

PubMed:36054329 PMC:PMC9771978

NIMH NIH HHS

Grant: R01 MH126933

NIMH NIH HHS

Grant: R00 MH117165

National Institutes of Health

Grant: 4R00MH117165-02

Nature and contribution of noncoding, regulatory mutations in neurodevelopmental disorders

National Institutes of Health

Grant: 1R01MH126933-01A1

Noncoding mutations in neurodevelopmental disorders

National Institutes of Health

hybridLicense: cc-by-nc-nd

publisherhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/humu.24455

publisherhttps://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.24455

publisherhttps://onlinelibrary.wiley.com/doi/full-xml/10.1002/humu.24455

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/9771978

Europe_PMChttps://europepmc.org/articles/PMC9771978

Fields of Study

0301 basic medicine03 medical and health sciences

MeSH Terms

HumansNeoplasmsMutationAllelesWhole Genome Sequencing

Keywords

1000 Genomes ProjectSimons Simplex CollectionDe Novo VariantsCell Line ArtifactsGpu Accelerated WorkflowWhole Genome SequencingNeoplasmsMutationHumansResearch ArticlesAlleles

Sustainable Development Goals

SDG 3: 3. Good health

de novo variant calling identifies cancer mutation signatures in the 1000 Genomes Project

FAIR Checklist

Authors (17)

Funding (5 grants)

Open Access

Topics

Annotations (Europe PMC)