Literature DB >> 29462260

Introducing whole-genome sequencing into routine cancer care: the Genomics England 100 000 Genomes Project.

C Turnbull1.   

Abstract

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Year:  2018        PMID: 29462260     DOI: 10.1093/annonc/mdy054

Source DB:  PubMed          Journal:  Ann Oncol        ISSN: 0923-7534            Impact factor:   32.976


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  16 in total

Review 1.  Emerging Role of Genomics and Cell-Free DNA in Breast Cancer.

Authors:  Lorenzo Gerratana; Andrew A Davis; Ami N Shah; Chenyu Lin; Carla Corvaja; Massimo Cristofanilli
Journal:  Curr Treat Options Oncol       Date:  2019-06-29

2.  Mapping the Read2/CTV3 controlled clinical terminologies to Phecodes in UK Biobank primary care electronic health records: implementation and evaluation.

Authors:  Spiros Denaxas; Ge Liu; Qiping Feng; Ghazaleh Fatemifar; Lisa Bastarache; Eric V Kerchberger; Aroon D Hingorani; Tom Lumbers; Josh F Peterson; Wei-Qi Wei; Harry Hemingway
Journal:  AMIA Annu Symp Proc       Date:  2022-02-21

3.  Substitution mutational signatures in whole-genome-sequenced cancers in the UK population.

Authors:  Andrea Degasperi; Xueqing Zou; Tauanne Dias Amarante; Andrea Martinez-Martinez; Gene Ching Chiek Koh; João M L Dias; Laura Heskin; Lucia Chmelova; Giuseppe Rinaldi; Valerie Ya Wen Wang; Arjun S Nanda; Aaron Bernstein; Sophie E Momen; Jamie Young; Daniel Perez-Gil; Yasin Memari; Cherif Badja; Scott Shooter; Jan Czarnecki; Matthew A Brown; Helen R Davies; Serena Nik-Zainal
Journal:  Science       Date:  2022-04-22       Impact factor: 63.714

4.  Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic Pipelines.

Authors:  Kyle Ellrott; Matthew H Bailey; Gordon Saksena; Kyle R Covington; Cyriac Kandoth; Chip Stewart; Julian Hess; Singer Ma; Kami E Chiotti; Michael McLellan; Heidi J Sofia; Carolyn Hutter; Gad Getz; David Wheeler; Li Ding
Journal:  Cell Syst       Date:  2018-03-28       Impact factor: 10.304

5.  Genetics in mainstream medicine: Finally within grasp to influence healthcare globally.

Authors:  Swaroop Aradhya; Robert L Nussbaum
Journal:  Mol Genet Genomic Med       Date:  2018-05-28       Impact factor: 2.183

6.  FIREVAT: finding reliable variants without artifacts in human cancer samples using etiologically relevant mutational signatures.

Authors:  Hyunbin Kim; Andy Jinseok Lee; Jongkeun Lee; Hyonho Chun; Young Seok Ju; Dongwan Hong
Journal:  Genome Med       Date:  2019-12-17       Impact factor: 11.117

7.  Genotyping structural variants in pangenome graphs using the vg toolkit.

Authors:  Glenn Hickey; David Heller; Jean Monlong; Jonas A Sibbesen; Jouni Sirén; Jordan Eizenga; Eric T Dawson; Erik Garrison; Adam M Novak; Benedict Paten
Journal:  Genome Biol       Date:  2020-02-12       Impact factor: 13.583

8.  The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children.

Authors:  Jacqueline A Odgis; Katie M Gallagher; Sabrina A Suckiel; Katherine E Donohue; Michelle A Ramos; Nicole R Kelly; Gabrielle Bertier; Christina Blackburn; Kaitlyn Brown; Lena Fielding; Jessenia Lopez; Karla Lopez Aguiniga; Estefany Maria; Jessica E Rodriguez; Monisha Sebastin; Nehama Teitelman; Dana Watnick; Nicole M Yelton; Avinash Abhyankar; Noura S Abul-Husn; Aaron Baum; Laurie J Bauman; Jules C Beal; Toby Bloom; Charlotte Cunningham-Rundles; George A Diaz; Siobhan Dolan; Bart S Ferket; Vaidehi Jobanputra; Patricia Kovatch; Thomas V McDonald; Patricia E McGoldrick; Rosamond Rhodes; Michael L Rinke; Mimsie Robinson; Arye Rubinstein; Lisa H Shulman; Christian Stolte; Steven M Wolf; Elissa Yozawitz; Randi E Zinberg; John M Greally; Bruce D Gelb; Carol R Horowitz; Melissa P Wasserstein; Eimear E Kenny
Journal:  Trials       Date:  2021-01-14       Impact factor: 2.279

9.  Genome analysis and knowledge-driven variant interpretation with TGex.

Authors:  Dvir Dahary; Yaron Golan; Yaron Mazor; Ofer Zelig; Ruth Barshir; Michal Twik; Tsippi Iny Stein; Guy Rosner; Revital Kariv; Fei Chen; Qiang Zhang; Yiping Shen; Marilyn Safran; Doron Lancet; Simon Fishilevich
Journal:  BMC Med Genomics       Date:  2019-12-30       Impact factor: 3.063

10.  High-Throughput Sequencing in Respiratory, Critical Care, and Sleep Medicine Research. An Official American Thoracic Society Workshop Report.

Authors:  Craig P Hersh; Ian M Adcock; Juan C Celedón; Michael H Cho; David C Christiani; Blanca E Himes; Naftali Kaminski; Rasika A Mathias; Deborah A Meyers; John Quackenbush; Susan Redline; Katrina A Steiling; Holly K Tabor; Martin D Tobin; Mark M Wurfel; Ivana V Yang; Gerard H Koppelman
Journal:  Ann Am Thorac Soc       Date:  2019-01
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