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...

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Detalles Bibliográficos
Autores principales: Wang, Xuewen, Huang, Meng, Budowle, Bruce, Ge, Jianye
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Genetics
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

Internet

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

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