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...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
BioMed Central Ltd
2021
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| Subjects: | |
| Online Access: | View Fulltext in Publisher |