Barely Significant
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Enhanced detection and genotyping of disease-associated tandem repeats using HMMSTR and targeted long-read sequencing.

Nucleic Acids Res · 2025 · PMC11754662 · PMID 39676678

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may be significantno p-value reported
The ability to accurately genotype similarly sized alleles can aid in diagnosis of repeat expansions where the threshold between normal or intermediate and pathogenic length is small, as well as aid in improving ill defined thresholds that may be significant to clinical outcomes.

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