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svCapture: efficient and specific detection of very low frequency structural variant junctions by error-minimized capture sequencing
Error-corrected sequencing of genomic targets enriched by probe-based capture has become a standard approach for detecting single-nucleotide variants (SNVs) and small insertion/deletions (indels) present at very low variant allele frequencies. Less attention has been given to comparable strategies f...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10167630/ https://www.ncbi.nlm.nih.gov/pubmed/37181851 http://dx.doi.org/10.1093/nargab/lqad042 |