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TRcaller: a novel tool for precise and ultrafast tandem repeat variant genotyping in massively parallel sequencing reads
Calling tandem repeat (TR) variants from DNA sequences is of both theoretical and practical significance. Some bioinformatics tools have been developed for detecting or genotyping TRs. However, little study has been done to genotyping TR alleles from long-read sequencing data, and the accuracy of ge...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10390829/ https://www.ncbi.nlm.nih.gov/pubmed/37533432 http://dx.doi.org/10.3389/fgene.2023.1227176 |