STRetch: detecting and discovering pathogenic short tandem repeat expansions-Reference-Cited by-同舟云学术

STRetch: detecting and discovering pathogenic short tandem repeat expansions

Published:2018-08-21 Issue:1 Volume:19 Page:
ISSN:1474-760X
Container-title:Genome Biology
language:en
Short-container-title:Genome Biol

Author:

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^ORCID

Funder

National Health and Medical Research Council

Publisher

Springer Science and Business Media LLC

Link

http://link.springer.com/content/pdf/10.1186/s13059-018-1505-2.pdf

Reference43 articles.

1. The 1000 Genomes Project Consortium, Abecasis GR, Altshuler D, Auton A, Brooks LD, Durbin RM, et al. A map of human genome variation from population-scale sequencing. Nature. 2010;467:1061–73.

2. Gemayel R, Vinces MD, Legendre M, Verstrepen KJ. Variable tandem repeats accelerate evolution of coding and regulatory sequences. Annu Rev Genet. 2010;44:445–77.

3. Orr HT, Zoghbi HY. Trinucleotide repeat disorders. Annu Rev Neurosci. 2007;30:575–621.

4. Hamada H, Seidman M, Howard BH, Gorman CM. Enhanced gene expression by the poly (dT-dG). poly (dC-dA) sequence. Mol Cell Biol. 1984;4:2622–30.

5. Li YY-CC, Korol AB, Fahima T, Beiles A, Nevo E. Microsatellites: genomic distribution, putative functions and mutational mechanisms: a review. Mol Ecol. 2002;11:2453–65.

Cited by 116 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A comparison of software for analysis of rare and common short tandem repeat (STR) variation using human genome sequences from clinical and population-based samples;PLOS ONE;2024-04-01

2. Sequence composition changes in short tandem repeats: heterogeneity, detection, mechanisms and clinical implications;Nature Reviews Genetics;2024-03-11

3. Sequencing and characterizing short tandem repeats in the human genome;Nature Reviews Genetics;2024-02-16

4. LUSTR: a new customizable tool for calling genome-wide germline and somatic short tandem repeat variants;BMC Genomics;2024-01-26

5. A phenome-wide association study of tandem repeat variation in 168,554 individuals from the UK Biobank;2024-01-23