Please use this identifier to cite or link to this item: https://doi.org/10.1186/s13073-022-01085-z
Title: REViewer: haplotype-resolved visualization of read alignments in and around tandem repeats
Authors: Dolzhenko, E
Weisburd, B
Ibañez, K
Rajan-Babu, IS
Anyansi, C
Bennett, MF
Billingsley, K
Carroll, A
Clamons, S
Danzi, MC
Deshpande, V
Ding, J
Fazal, S
Halman, A
Jadhav, B
Qiu, Y
Richmond, PA
Saunders, CT
Scheffler, K
van Vugt, JJFA
Zwamborn, RRAJ
Chong, SS 
Friedman, JM
Tucci, A 
Rehm, HL
Eberle, MA
Keywords: Repeat expansions
Short tandem repeats
Short-read sequencing data
Visualization
Alleles
Amyotrophic Lateral Sclerosis
Exome
Fragile X Mental Retardation Protein
Haplotypes
High-Throughput Nucleotide Sequencing
Humans
Tandem Repeat Sequences
Issue Date: 1-Dec-2022
Publisher: Springer Science and Business Media LLC
Citation: Dolzhenko, E, Weisburd, B, Ibañez, K, Rajan-Babu, IS, Anyansi, C, Bennett, MF, Billingsley, K, Carroll, A, Clamons, S, Danzi, MC, Deshpande, V, Ding, J, Fazal, S, Halman, A, Jadhav, B, Qiu, Y, Richmond, PA, Saunders, CT, Scheffler, K, van Vugt, JJFA, Zwamborn, RRAJ, Chong, SS, Friedman, JM, Tucci, A, Rehm, HL, Eberle, MA (2022-12-01). REViewer: haplotype-resolved visualization of read alignments in and around tandem repeats. Genome Medicine 14 (1) : 84-. ScholarBank@NUS Repository. https://doi.org/10.1186/s13073-022-01085-z
Abstract: Background: Expansions of short tandem repeats are the cause of many neurogenetic disorders including familial amyotrophic lateral sclerosis, Huntington disease, and many others. Multiple methods have been recently developed that can identify repeat expansions in whole genome or exome sequencing data. Despite the widely recognized need for visual assessment of variant calls in clinical settings, current computational tools lack the ability to produce such visualizations for repeat expansions. Expanded repeats are difficult to visualize because they correspond to large insertions relative to the reference genome and involve many misaligning and ambiguously aligning reads. Results: We implemented REViewer, a computational method for visualization of sequencing data in genomic regions containing long repeat expansions and FlipBook, a companion image viewer designed for manual curation of large collections of REViewer images. To generate a read pileup, REViewer reconstructs local haplotype sequences and distributes reads to these haplotypes in a way that is most consistent with the fragment lengths and evenness of read coverage. To create appropriate training materials for onboarding new users, we performed a concordance study involving 12 scientists involved in short tandem repeat research. We used the results of this study to create a user guide that describes the basic principles of using REViewer as well as a guide to the typical features of read pileups that correspond to low confidence repeat genotype calls. Additionally, we demonstrated that REViewer can be used to annotate clinically relevant repeat interruptions by comparing visual assessment results of 44 FMR1 repeat alleles with the results of triplet repeat primed PCR. For 38 of these alleles, the results of visual assessment were consistent with triplet repeat primed PCR. Conclusions: Read pileup plots generated by REViewer offer an intuitive way to visualize sequencing data in regions containing long repeat expansions. Laboratories can use REViewer and FlipBook to assess the quality of repeat genotype calls as well as to visually detect interruptions or other imperfections in the repeat sequence and the surrounding flanking regions. REViewer and FlipBook are available under open-source licenses at https://github.com/illumina/REViewer and https://github.com/broadinstitute/flipbook respectively.
Source Title: Genome Medicine
URI: https://scholarbank.nus.edu.sg/handle/10635/234474
ISSN: 1756-994X
DOI: 10.1186/s13073-022-01085-z
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