Literature DB >> 23463597

GEnomes Management Application (GEM.app): a new software tool for large-scale collaborative genome analysis.

Michael A Gonzalez1, Rafael F Acosta Lebrigio, Derek Van Booven, Rick H Ulloa, Eric Powell, Fiorella Speziani, Mustafa Tekin, Rebecca Schüle, Stephan Züchner.   

Abstract

Novel genes are now identified at a rapid pace for many Mendelian disorders, and increasingly, for genetically complex phenotypes. However, new challenges have also become evident: (1) effectively managing larger exome and/or genome datasets, especially for smaller labs; (2) direct hands-on analysis and contextual interpretation of variant data in large genomic datasets; and (3) many small and medium-sized clinical and research-based investigative teams around the world are generating data that, if combined and shared, will significantly increase the opportunities for the entire community to identify new genes. To address these challenges, we have developed GEnomes Management Application (GEM.app), a software tool to annotate, manage, visualize, and analyze large genomic datasets (https://genomics.med.miami.edu/). GEM.app currently contains ∼1,600 whole exomes from 50 different phenotypes studied by 40 principal investigators from 15 different countries. The focus of GEM.app is on user-friendly analysis for nonbioinformaticians to make next-generation sequencing data directly accessible. Yet, GEM.app provides powerful and flexible filter options, including single family filtering, across family/phenotype queries, nested filtering, and evaluation of segregation in families. In addition, the system is fast, obtaining results within 4 sec across ∼1,200 exomes. We believe that this system will further enhance identification of genetic causes of human disease.
© 2013 Wiley Periodicals, Inc.

Entities:  

Mesh:

Year:  2013        PMID: 23463597      PMCID: PMC4345138          DOI: 10.1002/humu.22305

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  24 in total

1.  VarSifter: visualizing and analyzing exome-scale sequence variation data on a desktop computer.

Authors:  Jamie K Teer; Eric D Green; James C Mullikin; Leslie G Biesecker
Journal:  Bioinformatics       Date:  2011-12-30       Impact factor: 6.937

2.  Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia.

Authors:  Elodie Martin; Rebecca Schüle; Katrien Smets; Agnès Rastetter; Amir Boukhris; José L Loureiro; Michael A Gonzalez; Emeline Mundwiller; Tine Deconinck; Marc Wessner; Ludmila Jornea; Andrés Caballero Oteyza; Alexandra Durr; Jean-Jacques Martin; Ludger Schöls; Chokri Mhiri; Foudil Lamari; Stephan Züchner; Peter De Jonghe; Edor Kabashi; Alexis Brice; Giovanni Stevanin
Journal:  Am J Hum Genet       Date:  2013-01-17       Impact factor: 11.025

3.  Evolution and functional impact of rare coding variation from deep sequencing of human exomes.

Authors:  Jacob A Tennessen; Abigail W Bigham; Timothy D O'Connor; Wenqing Fu; Eimear E Kenny; Simon Gravel; Sean McGee; Ron Do; Xiaoming Liu; Goo Jun; Hyun Min Kang; Daniel Jordan; Suzanne M Leal; Stacey Gabriel; Mark J Rieder; Goncalo Abecasis; David Altshuler; Deborah A Nickerson; Eric Boerwinkle; Shamil Sunyaev; Carlos D Bustamante; Michael J Bamshad; Joshua M Akey
Journal:  Science       Date:  2012-05-17       Impact factor: 47.728

4.  Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era.

Authors:  Nadine Norton; Peggy D Robertson; Mark J Rieder; Stephan Züchner; Evadnie Rampersaud; Eden Martin; Duanxiang Li; Deborah A Nickerson; Ray E Hershberger
Journal:  Circ Cardiovasc Genet       Date:  2012-02-15

5.  Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia.

Authors:  Christelle Tesson; Magdalena Nawara; Mustafa A M Salih; Rodrigue Rossignol; Maha S Zaki; Mohammed Al Balwi; Rebecca Schule; Cyril Mignot; Emilie Obre; Ahmed Bouhouche; Filippo M Santorelli; Christelle M Durand; Andrés Caballero Oteyza; Khalid H El-Hachimi; Abdulmajeed Al Drees; Naima Bouslam; Foudil Lamari; Salah A Elmalik; Mohammad M Kabiraj; Mohammed Z Seidahmed; Typhaine Esteves; Marion Gaussen; Marie-Lorraine Monin; Gabor Gyapay; Doris Lechner; Michael Gonzalez; Christel Depienne; Fanny Mochel; Julie Lavie; Ludger Schols; Didier Lacombe; Mohamed Yahyaoui; Ibrahim Al Abdulkareem; Stephan Zuchner; Atsushi Yamashita; Ali Benomar; Cyril Goizet; Alexandra Durr; Joseph G Gleeson; Frederic Darios; Alexis Brice; Giovanni Stevanin
Journal:  Am J Hum Genet       Date:  2012-11-21       Impact factor: 11.025

6.  The Human Gene Mutation Database (HGMD) and its exploitation in the fields of personalized genomics and molecular evolution.

Authors:  Peter D Stenson; Edward V Ball; Matthew Mort; Andrew D Phillips; Katy Shaw; David N Cooper
Journal:  Curr Protoc Bioinformatics       Date:  2012-09

7.  dSarm/Sarm1 is required for activation of an injury-induced axon death pathway.

Authors:  Jeannette M Osterloh; Jing Yang; Timothy M Rooney; A Nicole Fox; Robert Adalbert; Eric H Powell; Amy E Sheehan; Michelle A Avery; Rachel Hackett; Mary A Logan; Jennifer M MacDonald; Jennifer S Ziegenfuss; Stefan Milde; Ying-Ju Hou; Carl Nathan; Aihao Ding; Robert H Brown; Laura Conforti; Michael Coleman; Marc Tessier-Lavigne; Stephan Züchner; Marc R Freeman
Journal:  Science       Date:  2012-06-07       Impact factor: 47.728

8.  Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12.

Authors:  Gladys Montenegro; Adriana P Rebelo; James Connell; Rachel Allison; Carla Babalini; Michela D'Aloia; Pasqua Montieri; Rebecca Schüle; Hiroyuki Ishiura; Justin Price; Alleene Strickland; Michael A Gonzalez; Lisa Baumbach-Reardon; Tine Deconinck; Jia Huang; Giorgio Bernardi; Jeffery M Vance; Mark T Rogers; Shoji Tsuji; Peter De Jonghe; Margaret A Pericak-Vance; Ludger Schöls; Antonio Orlacchio; Evan Reid; Stephan Züchner
Journal:  J Clin Invest       Date:  2012-01-09       Impact factor: 14.808

9.  Exome sequencing identifies the cause of a mendelian disorder.

Authors:  Sarah B Ng; Kati J Buckingham; Choli Lee; Abigail W Bigham; Holly K Tabor; Karin M Dent; Chad D Huff; Paul T Shannon; Ethylin Wang Jabs; Deborah A Nickerson; Jay Shendure; Michael J Bamshad
Journal:  Nat Genet       Date:  2009-11-13       Impact factor: 38.330

10.  Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss.

Authors:  Oscar Diaz-Horta; Duygu Duman; Joseph Foster; Aslı Sırmacı; Michael Gonzalez; Nejat Mahdieh; Nikou Fotouhi; Mortaza Bonyadi; Filiz Başak Cengiz; Ibis Menendez; Rick H Ulloa; Yvonne J K Edwards; Stephan Züchner; Susan Blanton; Mustafa Tekin
Journal:  PLoS One       Date:  2012-11-30       Impact factor: 3.240

View more
  54 in total

Review 1.  Axons to Exons: the Molecular Diagnosis of Rare Neurological Diseases by Next-Generation Sequencing.

Authors:  Jodi Warman Chardon; Chandree Beaulieu; Taila Hartley; Kym M Boycott; David A Dyment
Journal:  Curr Neurol Neurosci Rep       Date:  2015-09       Impact factor: 5.081

Review 2.  Human genotype-phenotype databases: aims, challenges and opportunities.

Authors:  Anthony J Brookes; Peter N Robinson
Journal:  Nat Rev Genet       Date:  2015-11-10       Impact factor: 53.242

3.  A novel p.Leu(381)Phe mutation in presenilin 1 is associated with very early onset and unusually fast progressing dementia as well as lysosomal inclusions typically seen in Kufs disease.

Authors:  Natalia Dolzhanskaya; Michael A Gonzalez; Fiorella Sperziani; Shannon Stefl; Jeffrey Messing; Guang Y Wen; Emil Alexov; Stephan Zuchner; Milen Velinov
Journal:  J Alzheimers Dis       Date:  2014       Impact factor: 4.472

4.  Innovative genomic collaboration using the GENESIS (GEM.app) platform.

Authors:  Michael Gonzalez; Marni J Falk; Xiaowu Gai; Richard Postrel; Rebecca Schüle; Stephan Zuchner
Journal:  Hum Mutat       Date:  2015-08-12       Impact factor: 4.878

5.  Adult-onset painful axonal polyneuropathy caused by a dominant NAGLU mutation.

Authors:  Martine Tétreault; Michael Gonzalez; Marie-Josée Dicaire; Pierre Allard; Kalle Gehring; Diane Leblanc; Nadine Leclerc; Ronald Schondorf; Jean Mathieu; Stephan Zuchner; Bernard Brais
Journal:  Brain       Date:  2015-03-28       Impact factor: 13.501

6.  A novel mutation in VCP causes Charcot-Marie-Tooth Type 2 disease.

Authors:  Michael A Gonzalez; Shawna M Feely; Fiorella Speziani; Alleene V Strickland; Matt Danzi; Chelsea Bacon; Youjin Lee; Tsui-Fen Chou; Susan H Blanton; Conrad C Weihl; Stephan Zuchner; Michael E Shy
Journal:  Brain       Date:  2014-08-14       Impact factor: 13.501

7.  Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2.

Authors:  Alexander M Rossor; Emily C Oates; Hannah K Salter; Yang Liu; Sinead M Murphy; Rebecca Schule; Michael A Gonzalez; Mariacristina Scoto; Rahul Phadke; Caroline A Sewry; Henry Houlden; Albena Jordanova; Iyailo Tournev; Teodora Chamova; Ivan Litvinenko; Stephan Zuchner; David N Herrmann; Julian Blake; Janet E Sowden; Gyuda Acsadi; Michael L Rodriguez; Manoj P Menezes; Nigel F Clarke; Michaela Auer Grumbach; Simon L Bullock; Francesco Muntoni; Mary M Reilly; Kathryn N North
Journal:  Brain       Date:  2014-12-14       Impact factor: 13.501

8.  Motor protein mutations cause a new form of hereditary spastic paraplegia.

Authors:  Andrés Caballero Oteyza; Esra Battaloğlu; Levent Ocek; Tobias Lindig; Jennifer Reichbauer; Adriana P Rebelo; Michael A Gonzalez; Yasar Zorlu; Burcak Ozes; Dagmar Timmann; Benjamin Bender; Günther Woehlke; Stephan Züchner; Ludger Schöls; Rebecca Schüle
Journal:  Neurology       Date:  2014-05-07       Impact factor: 9.910

9.  MORC2 mutations cause axonal Charcot-Marie-Tooth disease with pyramidal signs.

Authors:  Obaid M Albulym; Marina L Kennerson; Matthew B Harms; Alexander P Drew; Anna H Siddell; Michaela Auer-Grumbach; Alan Pestronk; Anne Connolly; Robert H Baloh; Stephan Zuchner; Stephen W Reddel; Garth A Nicholson
Journal:  Ann Neurol       Date:  2016-01-13       Impact factor: 10.422

10.  Mutations in phospholipase DDHD2 cause autosomal recessive hereditary spastic paraplegia (SPG54).

Authors:  Michael Gonzalez; Sheela Nampoothiri; Cornelia Kornblum; Andrés Caballero Oteyza; Jochen Walter; Ioanna Konidari; William Hulme; Fiorella Speziani; Ludger Schöls; Stephan Züchner; Rebecca Schüle
Journal:  Eur J Hum Genet       Date:  2013-03-13       Impact factor: 4.246

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.