CV

     
09/2014–present PhD Student Computational Biology Group, Charité, Berlin.
05/2012–08/2014 Bioinformatician CeGaT, Tübingen
2009–2012 Master of Science in Bioinformatics University of Tübingen
2006–2009 Bachelor of Science in Bioinformatics University of Tübingen

Selected publications

See my Google Schloar profile for a complete list.

  • Jäger M, Schubach M, Zemojtel T, Reinert K, Church DM, Robinson PN. Alternate-locus aware variant calling in whole genome sequencing. Genome Medicine 2016;8:130
  • Smedley D, Schubach M, Jacobsen JOB, Köhler S, Zemojtel T, Spielmann M, Jäger M, Hochheiser H, Washington NL, McMurry JA, Haendel MA, Mungall CJ, Lewis SE, Groza T, Valentini G, Robinson PN. A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease. The American Journal of Human Genetics. 2016;99(3):595-606.
  • Smedley D, Jacobsen JOB, Jäger M, Köhler S, Holtgrewe M, Schubach M, Siragusa E, Zemojtel T, Buske OJ, Washington NL, Bone WP, Haendel MA, Robinson PN. Next-generation diagnostics and disease-gene discovery with the Exomiser. Nature protocols. 2015;10(12):2004–15.
  • Glöckle N, Kohl S, Mohr J, Scheurenbrand T, Sprecher A, Weisschuh N, Bernd A, Rudolph G, Schubach M, Poloschek C, Zrenner E, Biskup S, Berger W, Wissinger B, Neidhardt J. Panel-based Next Generation Sequencing as a reliable and efficient technique to detect mutations in unselected patients with retinal dystrophies. European Journal of Human Genetics. 2013;22(1):99–104.
  • Lemke JR, Riesch E, Scheurenbrand T, Schubach M, Wilhelm C, Steiner I, Hansen J, Courage C, Gallati S, Bürki S, Strozzi S, Goeggel Simonetti B, Grunt S, Steinlin M, Alber M, Wolff M, Klopstock T, Prott EC, Lorenz R, Spaich C, Rona S, Lakshminarasimhan M, Kröll J, Dorn T, Krämer G, Synofzik M, Becker F, Weber YG, Lerche H, Böhm D, Biskup S. Targeted next generation sequencing as a diagnostic tool in epileptic disorders. Epilepsia. 2012;53(8):1387–98.
  • Mitra S, Schubach M, Huson DH. Short clones or long clones? A simulation study on the use of paired reads in metagenomics. BMC Bioinformatics. 2010;11(S1):S12.

Awards

  • Poster award at the Arbeitsgemeinschaft Gendiagnostik (AGD) Annual Meeting 2016 in Potsdam. Title: “Genomiser, a framework to identify Mendelian regulatory mutations”

Contact

Max Schubach
Charité - Universitätsmedizin Berlin
Campus Virchow Klinikum
Institut für Medizinische Genetik und Humangenetik
Augustenburger Platz 1
13353 Berlin
Germany

Phone: +49/30/450 566006
Email: max.schubach at charite.de
Edit