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HAT: de novo variant calling for highly accurate short-read and long-read sequencing data

Bioinformatics(2024)10.1093/bioinformatics/btad775Source: DataRank Database

HAT: de novo variant calling for highly accurate short-read and long-read sequencing data is a research paper published in Bioinformatics (2024). On theSindex it has a DataRank of 0. It has been cited 12 times.

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Scored on demand from live citation data

Open Access12 citations

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (5 grants)OA: goldTopics (28)IDs (PubMed, PMC)Annotations (1)SDGs (1)

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 (2)

Tychele N. Turner ORCID,Jeffrey K. Ng

Live enrichment

PubMed:38175776 PMC:PMC10777354

National Institutes of Health

Grant: R00MH117165

National Institutes of Health

Grant: R01MH126933

Simons Foundation

Grant: #734069

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

goldLicense: cc-by

publisherhttps://academic.oup.com/bioinformatics/advance-article-pdf/doi/10.1093/bioinformatics/btad775/55024474/btad775.pdf

publisherhttps://academic.oup.com/bioinformatics/article-pdf/40/1/btad775/55265022/btad775.pdf

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC10777354/pdf/btad775.pdf

repositoryhttps://digitalcommons.wustl.edu/oa_4/2893

Europe_PMChttps://europepmc.org/articles/PMC10777354

Fields of Study

0301 basic medicine03 medical and health sciences

MeSH Terms

AnimalsHaresHumansTurtlesSequence Analysis, DNAGenome, HumanHigh-Throughput Nucleotide SequencingExomeWhole Genome Sequencing

Keywords

Original PaperGenomeWhole Genome SequencingGenome, HumanICTS (Institute of Clinical and Translational Sciences)High-Throughput Nucleotide SequencingDNASequence Analysis, DNAHaresArticleTurtlesMedicine and Health SciencesAnimalsHumansExomeSequence AnalysisHuman

Sustainable Development Goals

SDG 3: 3. Good health

HAT: de novo variant calling for highly accurate short-read and long-read sequencing data

FAIR Checklist

Authors (2)

Funding (5 grants)

Open Access

Topics

Annotations (Europe PMC)