SVhet: towards accurate detection of germline heterozygous deletions using short reads
Abstract Background Accurate structural variant detection from short-read sequencing data remains challenged by false positives, particularly for heterozygous deletions where reduced allelic support and coverage-based detection methods are ambiguous. Existing SV genotyping and filtering approaches s...
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| Главные авторы: | , , |
|---|---|
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
BMC
2025-12-01
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| Серии: | BMC Bioinformatics |
| Предметы: | |
| Online-ссылка: | https://doi.org/10.1186/s12859-025-06342-7 |
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