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BCFtools/liftover: an accurate and comprehensive tool to convert genetic variants across genome assemblies

Bioinformatics(2024)10.1093/bioinformatics/btae038Source: DataRank Database

BCFtools/liftover: an accurate and comprehensive tool to convert genetic variants across genome assemblies is a research paper published in Bioinformatics (2024). On theSindex it has a DataRank of 0. It has been cited 106 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access106 citations

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (3 grants)Impact (FWCI 42.61)OA: goldTopics (21)IDs (PubMed, PMC, OpenAlex)Annotations (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 (8)

Nicole B. Rockweiler ORCID,Bryan R. Gorman ORCID,Tim B. Bigdeli ORCID,M T Pato,Carlos N. Pato ORCID

Live enrichment

PubMed:38261650 PMC:PMC10832354 OpenAlex:https://openalex.org/W4391131250

National Institutes of Health

Grant: R01HG006855

National Institutes of Health

Grant: R01MH104964

National Institutes of Health

Grant: R01MH123451

FWCI

42.61

Citation Percentile

1.0%

Citation Trend

2024

2025

2026

goldLicense: cc-by

journalhttps://academic.oup.com/bioinformatics/advance-article-pdf/doi/10.1093/bioinformatics/btae038/56336087/btae038.pdf

publisherhttps://academic.oup.com/bioinformatics/advance-article-pdf/doi/10.1093/bioinformatics/btae038/56336087/btae038.pdf

publisherhttps://academic.oup.com/bioinformatics/article-pdf/40/2/btae038/56530632/btae038.pdf

journalhttps://doi.org/10.1093/bioinformatics/btae038

repositoryhttps://pubmed.ncbi.nlm.nih.gov/38261650

Fields of Study

Genomics and Rare DiseasesGenomics and Phylogenetic StudiesGenetic Associations and Epidemiology

MeSH Terms

AllelesSoftwareGenomicsINDEL MutationGenome-Wide Association Study

Keywords

Reference genomeGenomeIndelComputer scienceGenome projectComputational biologyGenomicsAnnotationData miningGeneticsBiologyGeneSingle-nucleotide polymorphism

BCFtools/liftover: an accurate and comprehensive tool to convert genetic variants across genome assemblies

FAIR Checklist

Authors (8)

Funding (3 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)