STRetch: detecting and discovering pathogenic short tandem repeat expansions

Short tandem repeat (STR) expansions have been identified as the causal DNA mutation in dozens of Mendelian diseases. Most existing tools for detecting STR variation with short reads do so within the read length and so are unable to detect the majority of pathogenic expansions. Here we present STRet...

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Detalles Bibliográficos
Autores principales: Dashnow, Harriet, Lek, Monkol, Phipson, Belinda, Halman, Andreas, Sadedin, Simon, Lonsdale, Andrew, Davis, Mark, Lamont, Phillipa, Clayton, Joshua S., Laing, Nigel G., MacArthur, Daniel G., Oshlack, Alicia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Method
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6102892/
https://www.ncbi.nlm.nih.gov/pubmed/30129428
http://dx.doi.org/10.1186/s13059-018-1505-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6102892/
https://www.ncbi.nlm.nih.gov/pubmed/30129428
http://dx.doi.org/10.1186/s13059-018-1505-2

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