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Inversion polymorphism in a complete human genome assembly

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.10.06.511148Source: DataRank Database

Inversion polymorphism in a complete human genome assembly is a research paper published in bioRxiv (Cold Spring Harbor Laboratory) (2022). On theSindex it has a DataRank of 0. It has been cited 5 times.

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Open Access5 citations

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (4 grants)OA: greenTopics (30)IDs (PubMed, OpenAlex)

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Authors (12)

William T. Harvey ORCID,Allison N. Rozanski ORCID,Jana Ebler ORCID,Wolfram Höps,Hufsah Ashraf ORCID

Live enrichment

PubMed:23304386 OpenAlex:https://openalex.org/W4302774270

National Institutes of Health

Grant: 5U24HG007497-07

Identifying and Characterizing the Full Spectrum of Haplotype-resolved Structural Variation in Human Genomes

National Institutes of Health

Grant: 5R01HG002385-15

Sequence and Assembly of Segmental Duplications

National Institutes of Health

Grant: 5R01HG010169-07

Sequence resolution of complex human genome structural variation

National Institutes of Health

Grant: 1U01HG010973-01

Representing structural haplotypes and complex genetic variation in pan-genome graphs

greenLicense: cc-by-nc-nd

repositoryhttps://www.biorxiv.org/content/biorxiv/early/2022/10/06/2022.10.06.511148.full.pdf

publisherhttps://syndication.highwire.org/content/doi/10.1101/2022.10.06.511148

repositoryhttps://doi.org/10.1101/2022.10.06.511148

https://doi.org/10.1186/s13059-023-02919-8

Fields of Study

Genomic variations and chromosomal abnormalitiesGenomics and Phylogenetic StudiesChromosomal and Genetic Variations0301 basic medicine0303 health sciences03 medical and health sciences

Keywords

GenomeHuman genomeReference genomeBiologyComputational biologyGeneticsTelomereStructural variationGeneT2T-CHM13Cancer ResearchGenomic structural variationPolymorphism, GeneticQH301-705.5Genome, HumanTopic 1: Genes, Cells and Cell-Based MedicineInversionShort ReportPericentromericQH426-470Chromosome InversionHumansBiology (General)Pathogenic copy number variant