Literature DB >> 35493723

FastViFi: Fast and accurate detection of (Hybrid) Viral DNA and RNA.

Sara Javadzadeh1, Utkrisht Rajkumar1, Nam Nguyen2, Shahab Sarmashghi3, Jens Luebeck4, Jingbo Shang1, Vineet Bafna1.   

Abstract

DNA viruses are important infectious agents known to mediate a large number of human diseases, including cancer. Viral integration into the host genome and the formation of hybrid transcripts are also associated with increased pathogenicity. The high variability of viral genomes, however requires the use of sensitive ensemble hidden Markov models that add to the computational complexity, often requiring > 40 CPU-hours per sample. Here, we describe FastViFi, a fast 2-stage filtering method that reduces the computational burden. On simulated and cancer genomic data, FastViFi improved the running time by 2 orders of magnitude with comparable accuracy on challenging data sets. Recently published methods have focused on identification of location of viral integration into the human host genome using local assembly, but do not extend to RNA. To identify human viral hybrid transcripts, we additionally developed ensemble Hidden Markov Models for the Epstein Barr virus (EBV) to add to the models for Hepatitis B (HBV), Hepatitis C (HCV) viruses and the Human Papillomavirus (HPV), and used FastViFi to query RNA-seq data from Gastric cancer (EBV) and liver cancer (HBV/HCV). FastViFi ran in <10 minutes per sample and identified multiple hybrids that fuse viral and human genes suggesting new mechanisms for oncoviral pathogenicity. FastViFi is available at https://github.com/sara-javadzadeh/FastViFi.
© The Author(s) 2022. Published by Oxford University Press on behalf of NAR Genomics and Bioinformatics.

Entities:  

Year:  2022        PMID: 35493723      PMCID: PMC9041341          DOI: 10.1093/nargab/lqac032

Source DB:  PubMed          Journal:  NAR Genom Bioinform        ISSN: 2631-9268


  41 in total

1.  High-throughput RNA sequencing-based virome analysis of 50 lymphoma cell lines from the Cancer Cell Line Encyclopedia project.

Authors:  Subing Cao; Michael J Strong; Xia Wang; Walter N Moss; Monica Concha; Zhen Lin; Tina O'Grady; Melody Baddoo; Claire Fewell; Rolf Renne; Erik K Flemington
Journal:  J Virol       Date:  2014-10-29       Impact factor: 5.103

2.  Extrachromosomal DNA in HPV-Mediated Oropharyngeal Cancer Drives Diverse Oncogene Transcription.

Authors:  John Pang; Nam Nguyen; Jens Luebeck; Vineet Bafna; Joseph Califano; Laurel Ball; Andrey Finegersh; Shuling Ren; Takuya Nakagawa; Mitchell Flagg; Sayed Sadat; Paul S Mischel; Guorong Xu; Kathleen Fisch; Theresa Guo; Gabrielle Cahill; Bharat Panuganti
Journal:  Clin Cancer Res       Date:  2021-09-21       Impact factor: 13.801

3.  Comprehensive genomic characterization of head and neck squamous cell carcinomas.

Authors: 
Journal:  Nature       Date:  2015-01-29       Impact factor: 49.962

Review 4.  Integration of Human Papillomavirus Genomes in Head and Neck Cancer: Is It Time to Consider a Paradigm Shift?

Authors:  Iain M Morgan; Laurence J DiNardo; Brad Windle
Journal:  Viruses       Date:  2017-08-03       Impact factor: 5.048

Review 5.  A Review of HPV-Related Head and Neck Cancer.

Authors:  Kazuhiro Kobayashi; Kenji Hisamatsu; Natsuko Suzui; Akira Hara; Hiroyuki Tomita; Tatsuhiko Miyazaki
Journal:  J Clin Med       Date:  2018-08-27       Impact factor: 4.241

6.  A systematic sequencing-based approach for microbial contaminant detection and functional inference.

Authors:  Sung-Joon Park; Satoru Onizuka; Masahide Seki; Yutaka Suzuki; Takanori Iwata; Kenta Nakai
Journal:  BMC Biol       Date:  2019-09-13       Impact factor: 7.431

7.  Skmer: assembly-free and alignment-free sample identification using genome skims.

Authors:  Shahab Sarmashghi; Kristine Bohmann; M Thomas P Gilbert; Vineet Bafna; Siavash Mirarab
Journal:  Genome Biol       Date:  2019-02-13       Impact factor: 13.583

8.  Aberrant integration of Hepatitis B virus DNA promotes major restructuring of human hepatocellular carcinoma genome architecture.

Authors:  Jonas Demeulemeester; Paula Otero; Clemency Jolly; Daniel García-Souto; Urtzi Garaigorta; Peter J Campbell; Hidewaki Nakagawa; Peter Van Loo; Eva G Álvarez; Ana Pequeño-Valtierra; Jorge Zamora; Marta Tojo; Javier Temes; Adrian Baez-Ortega; Bernardo Rodriguez-Martin; Ana Oitaben; Alicia L Bruzos; Mónica Martínez-Fernández; Kerstin Haase; Sonia Zumalave; Rosanna Abal; Jorge Rodríguez-Castro; Aitor Rodriguez-Casanova; Angel Diaz-Lagares; Yilong Li; Keiran M Raine; Adam P Butler; Iago Otero; Atsushi Ono; Hiroshi Aikata; Kazuaki Chayama; Masaki Ueno; Shinya Hayami; Hiroki Yamaue; Kazuhiro Maejima; Miguel G Blanco; Xavier Forns; Carmen Rivas; Juan Ruiz-Bañobre; Sofía Pérez-Del-Pulgar; Raúl Torres-Ruiz; Sandra Rodriguez-Perales; Jose M C Tubio
Journal:  Nat Commun       Date:  2021-11-25       Impact factor: 14.919

9.  SEPATH: benchmarking the search for pathogens in human tissue whole genome sequence data leads to template pipelines.

Authors:  Abraham Gihawi; Ghanasyam Rallapalli; Rachel Hurst; Colin S Cooper; Richard M Leggett; Daniel S Brewer
Journal:  Genome Biol       Date:  2019-10-22       Impact factor: 13.583

10.  GRIDSS2: comprehensive characterisation of somatic structural variation using single breakend variants and structural variant phasing.

Authors:  Daniel L Cameron; Jonathan Baber; Charles Shale; Jose Espejo Valle-Inclan; Nicolle Besselink; Arne van Hoeck; Roel Janssen; Edwin Cuppen; Peter Priestley; Anthony T Papenfuss
Journal:  Genome Biol       Date:  2021-07-12       Impact factor: 13.583

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.