Murdoch University Research Repository

Welcome to the Murdoch University Research Repository

The Murdoch University Research Repository is an open access digital collection of research
created by Murdoch University staff, researchers and postgraduate students.

Learn more

Recent advances in the detection of repeat expansions with short-read next-generation sequencing

Bahlo, M., Bennett, M.F., Degorski, P., Tankard, R.MORCID: 0000-0002-8847-9401, Delatycki, M.B. and Lockhart, P.J. (2018) Recent advances in the detection of repeat expansions with short-read next-generation sequencing. F1000Research, 7 . F1000 Faculty Rev-736.

[img]
Preview
PDF - Published Version
Download (757kB) | Preview
Free to read: https://doi.org/10.12688/f1000research.13980.1
*No subscription required

Abstract

Short tandem repeats (STRs), also known as microsatellites, are commonly defined as consisting of tandemly repeated nucleotide motifs of 2-6 base pairs in length. STRs appear throughout the human genome, and about 239,000 are documented in the Simple Repeats Track available from the UCSC (University of California, Santa Cruz) genome browser. STRs vary in size, producing highly polymorphic markers commonly used as genetic markers. A small fraction of STRs (about 30 loci) have been associated with human disease whereby one or both alleles exceed an STR-specific threshold in size, leading to disease. Detection of repeat expansions is currently performed with polymerase chain reaction-based assays or with Southern blots for large expansions. The tests are expensive and time-consuming and are not always conclusive, leading to lengthy diagnostic journeys for patients, potentially including missed diagnoses. The advent of whole exome and whole genome sequencing has identified the genetic cause of many genetic disorders; however, analysis pipelines are focused primarily on the detection of short nucleotide variations and short insertions and deletions (indels). Until recently, repeat expansions, with the exception of the smallest expansion (SCA6), were not detectable in next-generation short-read sequencing datasets and would have been ignored in most analyses. In the last two years, four analysis methods with accompanying software (ExpansionHunter, exSTRa, STRetch, and TREDPARSE) have been released. Although a comprehensive comparative analysis of the performance of these methods across all known repeat expansions is still lacking, it is clear that these methods are a valuable addition to any existing analysis pipeline. Here, we detail how to assess short-read data for evidence of expansions, reviewing all four methods and outlining their strengths and weaknesses. Implementation of these methods should lead to increased diagnostic yield of repeat expansion disorders for known STR loci and has the potential to detect novel repeat expansions.

Item Type: Journal Article
Murdoch Affiliation: School of Engineering and Information Technology
Publisher: F1000 Research Ltd
Copyright: © 2018 Bahlo M et al.
URI: http://researchrepository.murdoch.edu.au/id/eprint/41288
Item Control Page Item Control Page

Downloads

Downloads per month over past year