Accuracy of short tandem repeats genotyping tools in whole exome sequencing data [version 1; peer review: 2 approved, 1 approved with reservations]

Background: Short tandem repeats are an important source of genetic variation. They are highly mutable and repeat expansions are associated dozens of human disorders, such as Huntington's disease and spinocerebellar ataxias. Technical advantages in sequencing technology have made it possible to...

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Bibliographic Details
Main Authors: Andreas Halman, Alicia Oshlack
Format: Article
Language:English
Published: F1000 Research Ltd 2020-03-01
Series:F1000Research
Online Access:https://f1000research.com/articles/9-200/v1