Performance evaluation of structural variation detection using DNBSEQ whole-genome sequencing
Abstract Background DNBSEQ platforms have been widely used for variation detection, including single-nucleotide variants (SNVs) and short insertions and deletions (INDELs), which is comparable to Illumina. However, the performance and even characteristics of structural variations (SVs) detection usi...
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| Principais autores: | , , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BMC
2025-03-01
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| Serier: | BMC Genomics |
| Fag: | |
| Online adgang: | https://doi.org/10.1186/s12864-025-11494-0 |
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