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2-kupl: mapping-free variant detection from DNA-seq data of matched samples
BACKGROUND: The detection of genome variants, including point mutations, indels and structural variants, is a fundamental and challenging computational problem. We address here the problem of variant detection between two deep-sequencing (DNA-seq) samples, such as two human samples from an individua...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8180056/ https://www.ncbi.nlm.nih.gov/pubmed/34090332 http://dx.doi.org/10.1186/s12859-021-04185-6 |