Accurate imputation of inversions in human genomes using different algorithms and data sources.

doi:10.1093/nargab/lqag094

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Community

Back to search

Article

Accurate imputation of inversions in human genomes using different algorithms and data sources.

NAR genomics and bioinformatics - 1 Sept 2026

Yakymenko Illya, Mompart Adrià, Cáceres Mario

Abstract excerpt

Complex genomic regions harbor different structural arrangements that can mutate quite rapidly, which makes determining their functional effects very difficult. Characterization of inversions originated by homologous mechanisms is especially challenging due to the presence of inverted repeats at the breakpoints and the fact that most of them are recurrent. Imputation is a useful method to infer missing genotypes,...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Algorithms
Share to Chromosome Inversion
Share to Genome, Human
Share to Genotype
Share to Polymorphism, Single Nucleotide

Source

Open in PubMed Open full text

Identifiers

PMID: 42643609
DOI: 10.1093/nargab/lqag094
PMCID: PMC13504282

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics