USAT: a bioinformatic toolkit to facilitate interpretation and comparative visualization of tandem repeat sequences

BACKGROUND: Tandem repeats (TR), highly variable genomic variants, are widely used in individual identification, disease diagnostics, and evolutionary studies. The recent advances in sequencing technologies and bioinformatic tools facilitate calling TR haplotypes genome widely. Both length-based and...

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Detalles Bibliográficos
Autores principales: Wang, Xuewen, Budowle, Bruce, Ge, Jianye
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9675219/
https://www.ncbi.nlm.nih.gov/pubmed/36402991
http://dx.doi.org/10.1186/s12859-022-05021-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9675219/
https://www.ncbi.nlm.nih.gov/pubmed/36402991
http://dx.doi.org/10.1186/s12859-022-05021-1

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