Literature DB >> 35524567

TADeus2: a web server facilitating the clinical diagnosis by pathogenicity assessment of structural variations disarranging 3D chromatin structure.

Barbara Poszewiecka1, Victor Murcia Pienkowski2,3, Karol Nowosad4,5,6, Jérôme D Robin2, Krzysztof Gogolewski1, Anna Gambin1.   

Abstract

In recent years great progress has been made in identification of structural variants (SV) in the human genome. However, the interpretation of SVs, especially located in non-coding DNA, remains challenging. One of the reasons stems in the lack of tools exclusively designed for clinical SVs evaluation acknowledging the 3D chromatin architecture. Therefore, we present TADeus2 a web server dedicated for a quick investigation of chromatin conformation changes, providing a visual framework for the interpretation of SVs affecting topologically associating domains (TADs). This tool provides a convenient visual inspection of SVs, both in a continuous genome view as well as from a rearrangement's breakpoint perspective. Additionally, TADeus2 allows the user to assess the influence of analyzed SVs within flaking coding/non-coding regions based on the Hi-C matrix. Importantly, the SVs pathogenicity is quantified and ranked using TADA, ClassifyCNV tools and sampling-based P-value. TADeus2 is publicly available at https://tadeus2.mimuw.edu.pl.
© The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research.

Entities:  

Year:  2022        PMID: 35524567      PMCID: PMC9252839          DOI: 10.1093/nar/gkac318

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   19.160


  56 in total

1.  Structural variation and its effect on expression.

Authors:  Louise Harewood; Evelyne Chaignat; Alexandre Reymond
Journal:  Methods Mol Biol       Date:  2012

2.  Disruptions of topological chromatin domains cause pathogenic rewiring of gene-enhancer interactions.

Authors:  Darío G Lupiáñez; Katerina Kraft; Verena Heinrich; Peter Krawitz; Francesco Brancati; Eva Klopocki; Denise Horn; Hülya Kayserili; John M Opitz; Renata Laxova; Fernando Santos-Simarro; Brigitte Gilbert-Dussardier; Lars Wittler; Marina Borschiwer; Stefan A Haas; Marco Osterwalder; Martin Franke; Bernd Timmermann; Jochen Hecht; Malte Spielmann; Axel Visel; Stefan Mundlos
Journal:  Cell       Date:  2015-05-07       Impact factor: 41.582

3.  3DIV: A 3D-genome Interaction Viewer and database.

Authors:  Dongchan Yang; Insu Jang; Jinhyuk Choi; Min-Seo Kim; Andrew J Lee; Hyunwoong Kim; Junghyun Eom; Dongsup Kim; Inkyung Jung; Byungwook Lee
Journal:  Nucleic Acids Res       Date:  2018-01-04       Impact factor: 16.971

4.  Topological domains in mammalian genomes identified by analysis of chromatin interactions.

Authors:  Jesse R Dixon; Siddarth Selvaraj; Feng Yue; Audrey Kim; Yan Li; Yin Shen; Ming Hu; Jun S Liu; Bing Ren
Journal:  Nature       Date:  2012-04-11       Impact factor: 49.962

5.  Breakpoint Mapping of Symptomatic Balanced Translocations Links the EPHA6, KLF13 and UBR3 Genes to Novel Disease Phenotype.

Authors:  Victor Murcia Pienkowski; Marzena Kucharczyk; Małgorzata Rydzanicz; Barbara Poszewiecka; Katarzyna Pachota; Marlena Młynek; Piotr Stawiński; Agnieszka Pollak; Joanna Kosińska; Katarzyna Wojciechowska; Monika Lejman; Agata Cieślikowska; Dorota Wicher; Agnieszka Stembalska; Karolina Matuszewska; Anna Materna-Kiryluk; Anna Gambin; Krystyna Chrzanowska; Małgorzata Krajewska-Walasek; Rafał Płoski
Journal:  J Clin Med       Date:  2020-04-25       Impact factor: 4.241

6.  Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen).

Authors:  Erin Rooney Riggs; Erica F Andersen; Athena M Cherry; Sibel Kantarci; Hutton Kearney; Ankita Patel; Gordana Raca; Deborah I Ritter; Sarah T South; Erik C Thorland; Daniel Pineda-Alvarez; Swaroop Aradhya; Christa Lese Martin
Journal:  Genet Med       Date:  2019-11-06       Impact factor: 8.822

Review 7.  Unique roles of rare variants in the genetics of complex diseases in humans.

Authors:  Yukihide Momozawa; Keijiro Mizukami
Journal:  J Hum Genet       Date:  2020-09-18       Impact factor: 3.172

8.  Pervasive transcription of the human genome produces thousands of previously unidentified long intergenic noncoding RNAs.

Authors:  Matthew J Hangauer; Ian W Vaughn; Michael T McManus
Journal:  PLoS Genet       Date:  2013-06-20       Impact factor: 5.917

9.  Altered chromosomal topology drives oncogenic programs in SDH-deficient GISTs.

Authors:  William A Flavahan; Yotam Drier; Sarah E Johnstone; Matthew L Hemming; Daniel R Tarjan; Esmat Hegazi; Sarah J Shareef; Nauman M Javed; Chandrajit P Raut; Benjamin K Eschle; Prafulla C Gokhale; Jason L Hornick; Ewa T Sicinska; George D Demetri; Bradley E Bernstein
Journal:  Nature       Date:  2019-10-16       Impact factor: 49.962

10.  The mutational constraint spectrum quantified from variation in 141,456 humans.

Authors:  Konrad J Karczewski; Laurent C Francioli; Grace Tiao; Beryl B Cummings; Jessica Alföldi; Qingbo Wang; Ryan L Collins; Kristen M Laricchia; Andrea Ganna; Daniel P Birnbaum; Laura D Gauthier; Harrison Brand; Matthew Solomonson; Nicholas A Watts; Daniel Rhodes; Moriel Singer-Berk; Eleina M England; Eleanor G Seaby; Jack A Kosmicki; Raymond K Walters; Katherine Tashman; Yossi Farjoun; Eric Banks; Timothy Poterba; Arcturus Wang; Cotton Seed; Nicola Whiffin; Jessica X Chong; Kaitlin E Samocha; Emma Pierce-Hoffman; Zachary Zappala; Anne H O'Donnell-Luria; Eric Vallabh Minikel; Ben Weisburd; Monkol Lek; James S Ware; Christopher Vittal; Irina M Armean; Louis Bergelson; Kristian Cibulskis; Kristen M Connolly; Miguel Covarrubias; Stacey Donnelly; Steven Ferriera; Stacey Gabriel; Jeff Gentry; Namrata Gupta; Thibault Jeandet; Diane Kaplan; Christopher Llanwarne; Ruchi Munshi; Sam Novod; Nikelle Petrillo; David Roazen; Valentin Ruano-Rubio; Andrea Saltzman; Molly Schleicher; Jose Soto; Kathleen Tibbetts; Charlotte Tolonen; Gordon Wade; Michael E Talkowski; Benjamin M Neale; Mark J Daly; Daniel G MacArthur
Journal:  Nature       Date:  2020-05-27       Impact factor: 69.504

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