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      Recent advances in cancer fusion transcript detection

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          Abstract

          Extensive investigation of gene fusions in cancer has led to the discovery of novel biomarkers and therapeutic targets. To date, most studies have neglected chromosomal rearrangement-independent fusion transcripts and complex fusion structures such as double or triple-hop fusions, and fusion-circRNAs. In this review, we untangle fusion-related terminology and propose a classification system involving both gene and transcript fusions. We highlight the importance of RNA-level fusions and how long-read sequencing approaches can improve detection and characterization. Moreover, we discuss novel bioinformatic tools to identify fusions in long-read sequencing data and strategies to experimentally validate and functionally characterize fusion transcripts.

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          Most cited references100

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          Minimap2: pairwise alignment for nucleotide sequences

          Heng Li (2018)
          Recent advances in sequencing technologies promise ultra-long reads of ∼100 kb in average, full-length mRNA or cDNA reads in high throughput and genomic contigs over 100 Mb in length. Existing alignment programs are unable or inefficient to process such data at scale, which presses for the development of new alignment algorithms.
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            The Landscape of Circular RNA in Cancer

            Circular RNAs (circRNAs) are an intriguing class of RNA due to their covalently closed structure, high stability, and implicated roles in gene regulation. Here, we used an exome capture RNA sequencing protocol to detect and characterize circRNAs across >2,000 cancer samples. When compared against Ribo-Zero and RNase R, capture sequencing significantly enhanced the enrichment of circRNAs and preserved accurate circular-to-linear ratios. Using capture sequencing, we built the most comprehensive catalog of circRNA species to date: MiOncoCirc, the first database to be composed primarily of circRNAs directly detected in tumor tissues. Using MiOncoCirc, we identified candidate circRNAs to serve as biomarkers for prostate cancer and were able to detect circRNAs in urine. We further detected a novel class of circular transcripts, termed read-through circRNAs, that involved exons originating from different genes. MiOncoCirc will serve as a valuable resource for the development of circRNAs as diagnostic or therapeutic targets across cancer types.
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              Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome

              The DNA sequencing technologies in use today produce either highly accurate short reads or less-accurate long reads. We report the optimization of circular consensus sequencing (CCS) to improve the accuracy of single-molecule real-time (SMRT) sequencing (PacBio) and generate highly accurate (99.8%) long high-fidelity (HiFi) reads with an average length of 13.5 kilobases (kb). We applied our approach to sequence the well-characterized human HG002/NA24385 genome and obtained precision and recall rates of at least 99.91% for single-nucleotide variants (SNVs), 95.98% for insertions and deletions 15 megabases (Mb) and concordance of 99.997%, substantially outperforming assembly with less-accurate long reads.
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                Author and article information

                Contributors
                Journal
                Brief Bioinform
                Brief Bioinform
                bib
                Briefings in Bioinformatics
                Oxford University Press
                1467-5463
                1477-4054
                January 2023
                16 December 2022
                16 December 2022
                : 24
                : 1
                : bbac519
                Affiliations
                epartment of Molecular & Cell Biology, College of Public Health, Medical & Vet Sciences, James Cook University , Douglas, QLD 4811, Australia
                Centre for Tropical Bioinformatics and Molecular Biology, Australian Institute of Tropical Health and Medicine , James Cook University, Cairns 4878, Australia
                Gene and Stem Cell Therapy Program Centenary Institute, The University of Sydney , Camperdown, NSW 2050, Australia
                Faculty of Medicine & Health, The University of Sydney , Camperdown, NSW 2006, Australia
                Centre for Tropical Bioinformatics and Molecular Biology, Australian Institute of Tropical Health and Medicine , James Cook University, Cairns 4878, Australia
                Gene and Stem Cell Therapy Program Centenary Institute, The University of Sydney , Camperdown, NSW 2050, Australia
                Faculty of Medicine & Health, The University of Sydney , Camperdown, NSW 2006, Australia
                epartment of Molecular & Cell Biology, College of Public Health, Medical & Vet Sciences, James Cook University , Douglas, QLD 4811, Australia
                Storr Liver Centre, Westmead Institute for Medical Research, Westmead Hospital and University of Sydney , Sydney, New South Wales, Australia
                epartment of Molecular & Cell Biology, College of Public Health, Medical & Vet Sciences, James Cook University , Douglas, QLD 4811, Australia
                Centre for Tropical Bioinformatics and Molecular Biology, Australian Institute of Tropical Health and Medicine , James Cook University, Cairns 4878, Australia
                Author notes
                Corresponding author. Ulf Schmitz, Department of Molecular and Cell Biology, College of Public Health, Medical and Vet Sciences, James Cook University, Douglas, QLD 4811, Australia. E-mail: ulf.schmitz@ 123456jcu.edu.au
                Author information
                https://orcid.org/0000-0001-5319-0387
                https://orcid.org/0000-0001-5130-5224
                https://orcid.org/0000-0001-5806-4662
                Article
                bbac519
                10.1093/bib/bbac519
                9851307
                36527429
                e76fbb47-125f-4b88-82c0-c01765db0737
                © The Author(s) 2022. Published by Oxford University Press.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 26 July 2022
                : 11 October 2022
                : 31 October 2022
                Page count
                Pages: 12
                Funding
                Funded by: Tropical Australian Academic Health Centre;
                Award ID: SF0000321
                Funded by: Cancer Council NSW, DOI 10.13039/501100001102;
                Award ID: RG20-12
                Funded by: National Health and Medical Research Council, DOI 10.13039/501100000925;
                Award ID: #1196405
                Categories
                Review
                AcademicSubjects/SCI01060

                Bioinformatics & Computational biology
                fusion rna,chimeric rna,third-generation sequencing,trans-splicing,transcriptional readthrough

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