Benchmarking Whole Exome Sequencing in the German Network for Personalized Medicine

Author:

Menzel Michael,Martis-Thiele Mihaela,Goldschmid Hannah,Ott Alexander,Romanovsky Eva,Siemanowski-Hrach Janna,Seillier Lancelot,Brüchle Nadina Ortiz,Maurer Angela,Lehmann Kjong-Van,Begemann Matthias,Elbracht Miriam,Meyer Robert,Dintner Sebastian,Claus Rainer,Meier-Kolthoff Jan,Blanc Eric,Möbs Markus,Joosten Maria,Benary Manuela,Basitta Patrick,Hölscher Florian,Tischler Verena,Groß Thomas,Kutz Oliver,Prause Rebecca,William Doreen,Horny Kai,Goering Wolfgang,Sivalingam Sugirthan,Borkhardt Arndt,Blank Cornelia,Junk Stefanie,Yasin Layal,Moskalev Evgeny A.,Carta Maria Giulia,Ferrazzi Fulvia,Tögel Lars,Wolter Steffen,Adam Eugen,Matysiak Uta,Rosenthal Tessa,Dönitz Jürgen,Lehmann Ulrich,Schmidt Gunnar,Bartels Stephan,Hofmann Winfried,Hirsch Steffen,Dikow Nicola,Göbel Kirsten,Banan Rouzbeh,Hamelmann Stefan,Fink Annette,Ball Markus,Neumann Olaf,Rehker Jan,Kloth Michael,Murtagh Justin,Hartmann Nils,Jurmeister Phillip,Mock Andreas,Kumbrink Jörg,Jung Andreas,Mayr Eva-Maria,Jacob Anne,Trautmann Marcel,Kirmse Santina,Falkenberg Kim,Ruckert Christian,Hirsch Daniela,Immel Alexander,Dietmaier Wolfgang,Haack Tobias,Marienfeld Ralf,Fürstberger Axel,Niewöhner Jakob,Gerstenmaier Uwe,Eberhardt Timo,Greif Phillip,Appenzeller Silke,Maurus Katja,Doll Julia,Jelting Yvonne,Jonigk Danny,Märkl Bruno,Beule Dieter,Horst David,Wulf Anna-Lena,Aust Daniela,Werner Martin,Reuter-Jessen Kirsten,Ströbel Philipp,Auber Bernd,Sahm Felix,Merkelbach-Bruse Sabine,Siebolts Udo,Roth Wilfried,Lassmann Silke,Klauschen Frederick,Gaisa Nadine T.,Weichert Wilko,Evert Matthias,Armeanu-Ebinger Sorin,Ossowski Stephan,Schroeder Christopher,Schaaf Christian P.,Malek Nisar,Schirmacher Peter,Kazdal Daniel,Pfarr Nicole,Budczies Jan,Stenzinger Albrecht

Publisher

Elsevier BV

Reference23 articles.

1. Multicentric pilot study to standardize clinical whole exome sequencing (WES) for cancer patients;Menzel;NPJ Precis Oncol,2023

2. Pan-cancer analysis of genomic scar patterns caused by homologous repair deficiency (HRD);Rempel;Npj Precis Oncol,2022

3. Optimizing panel-based tumor mutational burden (TMB) measurement;Budczies;Annals of oncology: official journal of the European Society for Medical Oncology,2019

4. Comparison of actionable events detected in cancer genomes by whole-genome sequencing, in silico whole-exome and mutation panels;Ramarao-Milne;ESMO Open,2022

5. Feasibility of high-throughput sequencing in clinical routine cancer care: lessons from the cancer pilot project of the France Genomic Medicine 2025 plan;Auzanneau;ESMO Open,2020

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