ArticleGenome research2026
Read-level genotyping of short tandem repeats using long reads and single-nucleotide variation with STRkit.
Article in Genome research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Toward the clinical application of long-read sequencing in repeat-expansion disorders.Nature genetics · 2026Review
- Genome-wide detection and clinical prioritization of tandem repeat outliers using long-read sequencing.medRxiv : the preprint server for health sciences · 2026Article
- Detection of short tandem repeats in the cattle genome: a comparison of bioinformatic tools.BMC genomics · 2026Article
- A comprehensive assessment of tandem repeat genotyping methods for Nanopore long-read genomes.bioRxiv : the preprint server for biology · 2026Article
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Authors and funding
3 authors.
Funding
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Abstract
Variation in short tandem repeats (STRs) is implicated in Mendelian disease and complex traits but can be difficult to resolve with short-read genome sequencing. We present STRkit, a software package for genotyping STRs using long-read sequencing (LRS) that uses proximate single-nucleotide variants to improve genotyping accuracy without a priori haplotype information. We show that STRkit has unique strengths versus other methods: It can use data from both major LRS technologies (Pacific Biosciences HiFi [PacBio] and Oxford Nanopore Technologies [ONT]) to output both allele- and read-level copy number and sequence; it performs best in benchmarking with F1 scores of 0.9631 and 0.9544 with PacBio and ONT data, respectively; it achieves higher rates of Mendelian consistency than other genotyping tools; and it is open source software. STRkit's features open up new possibilities for association testing, assessing patterns of STR inheritance and better understanding the functional effects of these notable repeat elements.
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