Literature DB >> 36262335

The third international hackathon for applying insights into large-scale genomic composition to use cases in a wide range of organisms.

Kimberly Walker1, Divya Kalra1, Rebecca Lowdon2, Guangyi Chen3,4, David Molik5, Daniela C Soto6, Fawaz Dabbaghie3,7, Ahmad Al Khleifat8, Medhat Mahmoud1, Luis F Paulin1, Muhammad Sohail Raza9, Susanne P Pfeifer10, Daniel Paiva Agustinho11, Elbay Aliyev12, Pavel Avdeyev13, Enrico R Barrozo14, Sairam Behera1, Kimberley Billingsley15, Li Chuin Chong16, Deepak Choubey17, Wouter De Coster18,19, Yilei Fu20, Alejandro R Gener21, Timothy Hefferon22, David Morgan Henke23, Wolfram Höps24, Anastasia Illarionova25, Michael D Jochum14, Maria Jose26, Rupesh K Kesharwani1, Sree Rohit Raj Kolora27, Jędrzej Kubica28, Priya Lakra29, Damaris Lattimer30, Chia-Sin Liew31, Bai-Wei Lo32, Chunhsuan Lo33, Anneri Lötter34, Sina Majidian35, Suresh Kumar Mendem36, Rajarshi Mondal37, Hiroko Ohmiya38, Nasrin Parvin37, Carolina Peralta39, Chi-Lam Poon40, Ramanandan Prabhakaran41, Marie Saitou42, Aditi Sammi43, Philippe Sanio44, Nicolae Sapoval20, Najeeb Syed12, Todd Treangen20, Gaojianyong Wang45, Tiancheng Xu20, Jianzhi Yang46, Shangzhe Zhang47, Weiyu Zhou48, Fritz J Sedlazeck1, Ben Busby49.   

Abstract

In October 2021, 59 scientists from 14 countries and 13 U.S. states collaborated virtually in the Third Annual Baylor College of Medicine & DNANexus Structural Variation hackathon. The goal of the hackathon was to advance research on structural variants (SVs) by prototyping and iterating on open-source software. This led to nine hackathon projects focused on diverse genomics research interests, including various SV discovery and genotyping methods, SV sequence reconstruction, and clinically relevant structural variation, including SARS-CoV-2 variants. Repositories for the projects that participated in the hackathon are available at https://github.com/collaborativebioinformatics. Copyright:
© 2022 Walker K et al.

Entities:  

Keywords:  Cancer; Covid-19; Hackathon; Long-reads; NGS; Structural variants; Tomatoes; Viral integration; k-mer

Mesh:

Year:  2022        PMID: 36262335      PMCID: PMC9557141          DOI: 10.12688/f1000research.110194.1

Source DB:  PubMed          Journal:  F1000Res        ISSN: 2046-1402


  122 in total

Review 1.  Expandable DNA repeats and human disease.

Authors:  Sergei M Mirkin
Journal:  Nature       Date:  2007-06-21       Impact factor: 49.962

2.  Spike mutation D614G alters SARS-CoV-2 fitness.

Authors:  Jessica A Plante; Yang Liu; Jianying Liu; Hongjie Xia; Bryan A Johnson; Kumari G Lokugamage; Xianwen Zhang; Antonio E Muruato; Jing Zou; Camila R Fontes-Garfias; Divya Mirchandani; Dionna Scharton; John P Bilello; Zhiqiang Ku; Zhiqiang An; Birte Kalveram; Alexander N Freiberg; Vineet D Menachery; Xuping Xie; Kenneth S Plante; Scott C Weaver; Pei-Yong Shi
Journal:  Nature       Date:  2020-10-26       Impact factor: 49.962

3.  Comparative analysis of de novo assemblers for variation discovery in personal genomes.

Authors:  Shulan Tian; Huihuang Yan; Eric W Klee; Michael Kalmbach; Susan L Slager
Journal:  Brief Bioinform       Date:  2018-09-28       Impact factor: 11.622

4.  Emergence of genomic diversity and recurrent mutations in SARS-CoV-2.

Authors:  Lucy van Dorp; Mislav Acman; Damien Richard; Liam P Shaw; Charlotte E Ford; Louise Ormond; Christopher J Owen; Juanita Pang; Cedric C S Tan; Florencia A T Boshier; Arturo Torres Ortiz; François Balloux
Journal:  Infect Genet Evol       Date:  2020-05-05       Impact factor: 3.342

5.  Intra-Host Diversity of SARS-Cov-2 Should Not Be Neglected: Case of the State of Victoria, Australia.

Authors:  Alix Armero; Nicolas Berthet; Jean-Christophe Avarre
Journal:  Viruses       Date:  2021-01-19       Impact factor: 5.048

6.  Fast and accurate short read alignment with Burrows-Wheeler transform.

Authors:  Heng Li; Richard Durbin
Journal:  Bioinformatics       Date:  2009-05-18       Impact factor: 6.937

7.  Human viruses: discovery and emergence.

Authors:  Mark Woolhouse; Fiona Scott; Zoe Hudson; Richard Howey; Margo Chase-Topping
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2012-10-19       Impact factor: 6.237

8.  DELLY: structural variant discovery by integrated paired-end and split-read analysis.

Authors:  Tobias Rausch; Thomas Zichner; Andreas Schlattl; Adrian M Stütz; Vladimir Benes; Jan O Korbel
Journal:  Bioinformatics       Date:  2012-09-15       Impact factor: 6.937

Review 9.  Alignment-free sequence comparison: benefits, applications, and tools.

Authors:  Andrzej Zielezinski; Susana Vinga; Jonas Almeida; Wojciech M Karlowski
Journal:  Genome Biol       Date:  2017-10-03       Impact factor: 13.583

10.  Heterogeneity in HIV and cellular transcription profiles in cell line models of latent and productive infection: implications for HIV latency.

Authors:  Sushama Telwatte; Sara Morón-López; Dvir Aran; Peggy Kim; Christine Hsieh; Sunil Joshi; Mauricio Montano; Warner C Greene; Atul J Butte; Joseph K Wong; Steven A Yukl
Journal:  Retrovirology       Date:  2019-11-11       Impact factor: 4.602

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