The mutational dynamics of short tandem repeats in large, multigenerational families
Abstract Background Short tandem repeats (STRs) compose approximately 3% of the genome, and mutations at STR loci have been linked to dozens of human diseases including amyotrophic lateral sclerosis, Friedreich ataxia, Huntington disease, and fragile X syndrome. Improving our understanding of these...
Main Authors: | Cody J. Steely, W. Scott Watkins, Lisa Baird, Lynn B. Jorde |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2022-12-01
|
Series: | Genome Biology |
Subjects: | |
Online Access: | https://doi.org/10.1186/s13059-022-02818-4 |
Similar Items
-
Mutation Studies of 31 Highly Mutated Y-chromosomal Short Tandem Repeat Systems in the Han Population of Northern China
by: Shicheng Hao, et al.
Published: (2024-06-01) -
Mutation analysis of 21 autosomal short tandem repeats in Han population from Hunan, China
by: Wei Xu, et al.
Published: (2019-04-01) -
Editorial: Could Speciation Across Evolution be Governed by Genetic Switch Codes at Short Tandem Repeats?
by: Mina Ohadi
Published: (2017-03-01) -
Evaluation of allelic alterations in short tandem repeats in papillary thyroid cancer
by: Zhen Dang, et al.
Published: (2020-04-01) -
Genome-wide detection of short tandem repeat expansions by long-read sequencing
by: Qian Liu, et al.
Published: (2020-12-01)