Literature DB >> 33893808

MutationTaster2021.

Robin Steinhaus1,2, Sebastian Proft1,2, Markus Schuelke3,4, David N Cooper5, Jana Marie Schwarz3, Dominik Seelow1,2.   

Abstract

Here we present an update to MutationTaster, our DNA variant effect prediction tool. The new version uses a different prediction model and attains higher accuracy than its predecessor, especially for rare benign variants. In addition, we have integrated many sources of data that only became available after the last release (such as gnomAD and ExAC pLI scores) and changed the splice site prediction model. To more easily assess the relevance of detected known disease mutations to the clinical phenotype of the patient, MutationTaster now provides information on the diseases they cause. Further changes represent a major overhaul of the interfaces to increase user-friendliness whilst many changes under the hood have been designed to accelerate the processing of uploaded VCF files. We also offer an API for the rapid automated query of smaller numbers of variants from within other software. MutationTaster2021 integrates our disease mutation search engine, MutationDistiller, to prioritise variants from VCF files using the patient's clinical phenotype. The novel version is available at https://www.genecascade.org/MutationTaster2021/. This website is free and open to all users and there is no login requirement.
© The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research.

Entities:  

Year:  2021        PMID: 33893808     DOI: 10.1093/nar/gkab266

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  16 in total

1.  FABIAN-variant: predicting the effects of DNA variants on transcription factor binding.

Authors:  Robin Steinhaus; Peter N Robinson; Dominik Seelow
Journal:  Nucleic Acids Res       Date:  2022-05-26       Impact factor: 19.160

2.  Rare Variants in Novel Candidate Genes Associated With Nonsyndromic Patent Ductus Arteriosus Identified With Whole-Exome Sequencing.

Authors:  Ying Gao; Dan Wu; Bo Chen; Yinghui Chen; Qi Zhang; Pengjun Zhao
Journal:  Front Genet       Date:  2022-06-06       Impact factor: 4.772

3.  A Novel Frame-Shift Mutation in SCNN1B Identified in a Chinese Family Characterized by Early-Onset Hypertension.

Authors:  Yi-Ting Lu; Xin-Chang Liu; Ze-Ming Zhou; Di Zhang; Lin Sun; Ying Zhang; Peng Fan; Lin Zhang; Ya-Xin Liu; Fang Luo; Xian-Liang Zhou
Journal:  Front Cardiovasc Med       Date:  2022-06-14

4.  Screening of the TMEM151A Gene in Patients With Paroxysmal Kinesigenic Dyskinesia and Other Movement Disorders.

Authors:  Ling-Yan Ma; Lin Han; Meng Niu; Lu Chen; Ya-Zhen Yu; Tao Feng
Journal:  Front Neurol       Date:  2022-05-30       Impact factor: 4.086

5.  Clinical and genetic spectrum of a large cohort of patients with δ-sarcoglycan muscular dystrophy.

Authors:  Jorge Alonso-Pérez; Lidia González-Quereda; Claudio Bruno; Chiara Panicucci; Afagh Alavi; Shahriar Nafissi; Yalda Nilipour; Edmar Zanoteli; Lucas Michielon de Augusto Isihi; Béla Melegh; Kinga Hadzsiev; Nuria Muelas; Juan J Vílchez; Mario Emilio Dourado; Naz Kadem; Gultekin Kutluk; Muhammad Umair; Muhammad Younus; Elena Pegorano; Luca Bello; Thomas O Crawford; Xavier Suárez-Calvet; Ana Töpf; Michela Guglieri; Chiara Marini-Bettolo; Pia Gallano; Volker Straub; Jordi Díaz-Manera
Journal:  Brain       Date:  2022-04-18       Impact factor: 15.255

6.  TELO-SCOPE study: a randomised, double-blind, placebo-controlled, phase 2 trial of danazol for short telomere related pulmonary fibrosis.

Authors:  John A Mackintosh; Maria Pietsch; Viviana Lutzky; Debra Enever; Sandra Bancroft; Simon H Apte; Maxine Tan; Stephanie T Yerkovich; Joanne L Dickinson; Hilda A Pickett; Hiran Selvadurai; Christopher Grainge; Nicole S Goh; Peter Hopkins; Ian Glaspole; Paul N Reynolds; Jeremy Wrobel; Adam Jaffe; Tamera J Corte; Daniel C Chambers
Journal:  BMJ Open Respir Res       Date:  2021-12

7.  Fast and Easy Nanopore Sequencing Workflow for Rapid Genetic Testing of Familial Hypercholesterolemia.

Authors:  Muhidien Soufi; Simon Bedenbender; Volker Ruppert; Bilgen Kurt; Bernhard Schieffer; Juergen R Schaefer
Journal:  Front Genet       Date:  2022-02-09       Impact factor: 4.599

8.  Identification, analysis of deleterious SNPs of the human GSR gene and their effects on the structure and functions of associated proteins and other diseases.

Authors:  Bharti Vyas; Ratul Bhowmik; Mymoona Akhter; Farhan Jalees Ahmad
Journal:  Sci Rep       Date:  2022-03-31       Impact factor: 4.379

9.  VHL-P138R and VHL-L163R Novel Variants: Mechanisms of VHL Pathogenicity Involving HIF-Dependent and HIF-Independent Actions.

Authors:  Cecilia Mathó; María Celia Fernández; Jenner Bonanata; Xian-De Liu; Ayelen Martin; Ana Vieites; Gabriela Sansó; Marta Barontini; Eric Jonasch; E Laura Coitiño; Patricia Alejandra Pennisi
Journal:  Front Endocrinol (Lausanne)       Date:  2022-03-21       Impact factor: 5.555

10.  Complex Autism Spectrum Disorder with Epilepsy, Strabismus and Self-Injurious Behaviors in a Patient with a De Novo Heterozygous POLR2A Variant.

Authors:  Daniel R Evans; Ying Qiao; Brett Trost; Kristina Calli; Sally Martell; Steven J M Jones; Stephen W Scherer; M E Suzanne Lewis
Journal:  Genes (Basel)       Date:  2022-03-07       Impact factor: 4.096

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