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