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Allele detection using k-mer-based sequencing error profiles
MOTIVATION: For genotype and haplotype inference, typically, sequencing reads aligned to a reference genome are used. The alignments identify the genomic origin of the reads and help to infer the absence or presence of sequence variants in the genome. Since long sequencing reads often come with high...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Oxford University Press
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10625474/ https://www.ncbi.nlm.nih.gov/pubmed/37928341 http://dx.doi.org/10.1093/bioadv/vbad149 |