Publikationen von F. Mertes

G. D. Poznik, Y. Xue, F. L. Mendez, T. F. Willems, A. Massaia, M. A. Wilson Sayres, Consortium The 1000 Genomes Projekt, H. Lehrach, R. Sudbrak, M. W. Albrecht, V. Amstislavskiy, T. A. Borodina, M. Lienhard, F. Mertes, M. Sultan, B. Timmermann, and M.-L. Yaspo, "Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences," Nature Genetics 48 (6), 593-599 (2016).

Steven McGinn, David Bauer, Thomas Bretfort, Florian Mertes, Hans Lehrach, and Sascha Sauer, "New technologies for DNA analysis - a review of the READNA Project.," New biotechnology 33 (3), 311-330 (2016).

Florian Mertes, Björn Lichtner, Heiner Kuhl, Mirjam Blattner , Jörg Otte, Wasco Wruck, Bernd Timmermann, Hans Lehrach, and James Adjaye, "Combined ultra-low input mRNA and whole-genome sequencing of human embryonic stem cells," BMC Genomics 16, 16:925 (2015).

V. Colonna, Q. Ayub, Y. Chen, L. Pagani, P. Luisi, M. Pybus, E. Garrison, Y. Xue, C. Tyler-Smith, Consortium 1000 Genomes Project, R. Sudbrak, M. Albrecht, V. Amstislavskiy, T. A. Borodina, A. Dahl, A. Davydov, R. Herwig, P. Marquardt, F. Mertes, W. Nietfeld, D. Parkhomchuk, A. V. Soldatov, B. Timmermann, M. Tolzmann, H. Lehrach, and M. L. Yaspo, "Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences," Genome Biology: Biology for the Post-Genomic Era 15 (6), R88 (2014).

O. Delaneau, J. Marchini, Consortium 1000 Genomes Project, H. Lehrach, R. Sudbrak, V. S. Amstislavskiy, M. Lienhard, F. Mertes, M. Sultan, B. Timmermann, M. L. Yaspo, and R. Herwig, "Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel," Nature Communications 5, 5:3934 (2014).

E. Khurana, Y. Fu, V. Colonna, X. J. Mu, H. M. Kang, T. Lappalainen, A. Sboner, L. Lochovsky, J. Chen, A. Harmanci, J. Das, A. Abyzov, S. Balasubramanian, K. Beal, D. Chakravarty, D. Challis, Y. Chen, D. Clarke, L. Clarke, F. Cunningham, U. S. Evani, P. Flicek, R. Fragoza, E. Garrison, R. Gibbs, Z. H. Gumus, J. Herrero, N. Kitabayashi, Y. Kong, K. Lage, V. Liluashvili, S. M. Lipkin, D. G. MacArthur, G. Marth, D. Muzny, T. H. Pers, G. R. Ritchie, J. A. Rosenfeld, C. Sisu, X. Wei, M. Wilson, Y. Xue, F. Yu, Consortium 1000 Genomes Project, H. Lehrach, R. Sudbrak, M. W. Albrecht, V. Amstislavskiy, T. A. Borodina, M. Lienhard, F. Mertes, M. Sultan, B. Timmermann, M. L. Yaspo, E. T. Dermitzakis, H. Yu, M. A. Rubin, C. Tyler-Smith, and M. Gerstein, "Integrative annotation of variants from 1092 humans: application to cancer genomics," Science 342 (6154), 1235587-1235587 (2013).

Goncalo R. Abecasis, Adam Auton, Lisa D. Brooks, Mark A. DePristo, Richard M. Durbin, Robert E. Handsaker, Hyun Min Kang, Gabor T. Marth, Gil A. McVean, The 1000 Genomes Project Consortium, Ralf Sudbrak, Marcus Albrecht, Vyacheslav Amstislavskiy, Tatiana A. Borodina, Alexey Davydov, Ralf Herwig, Matthias Lienhard, Florian Mertes, Marc Sultan, Bernd Timmermann, Marie L. Yaspo, and Hans Lehrach, "An integrated map of genetic variation from 1,092 human genomes," Nature 491 (7422), 56-65 (2012).

Robert Querfurth, Axel Fischer, Michal R. Schweiger, Hans Lehrach, and Florian Mertes, "Creation and application of immortalized bait libraries for targeted enrichment and next-generation sequencing," Biotechniques 52 (6), 375-380 (2012).

The 1000 Genomes Project Consortium, Ralf Sudbrak, Marcus Albrecht, Vyacheslav Amstislavskiy, Tatiana A. Borodina, Andreas Dahl, Alexey Davydov, Ralf Herwig, Peter Marquardt, Florian Mertes, Wilfried Nietfeld, Dmitri Parkhomchuk, Aleksey Soldatov, Bernd Timmermann, Marius Tolzmann, and Hans Lehrach, "The 1000 Genomes Project: data management and community access," Nature methods 9 (5), 459-462 (2012).

D. G. MacArthur, S. Balasubramanian, A. Frankish, Consortium 1000 Genomes Project, R. Sudbrak, M. W. Albrecht , V. Amstislavskiy, T. A. Borodina, Andreas Dahl, A. Davydov, R. Herwig, P. Marquardt, F. Mertes, W. Nietfeld, D. Parkhomchuk, A. Soldatov, B. Timmermann, M. Tolzmann, and H. Lehrach, "A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes," Science 335 (6070), 823-828 (2012).

F. Mertes, A. Elsharawy, S. Sauer, J. M. van Helvoort, P. J. van der Zaag, A. Franke, M. Nilsson, H. Lehrach, and A. J. Brookes, "Targeted enrichment of genomic DNA regions for next-generation sequencing," Brief Funct Genomics 10 (6), 374-86 (2011).

F. Mertes, K. Biens, H. Lehrach, M. Wagner, and A. Dahl, "High-throughput Universal Probe Salmonella Serotyping (UPSS) by nanoPCR.," J Microbiol Methods 83 (2), 217-223 (2010).

A. Dahl, F. Mertes, B. Timmermann, and H. Lehrach, "The application of massively parallel sequencing technologies in diagnostics," F1000 Biology Reports 2, 2:59-2:59 (2010).

A. Dahl, F. Mertes, U. Marchfelder, S. Boerno, A. Fischer, M. Schweiger, and H. Lehrach, "Bewertung der SOLiD-Sequenzierungsplattform aus Nutzerperspektive," Laborwelt 11 (1), 8-10 (2010).

Lei Mao, Claus Zabel, Marion Herrmann, Tobias Nolden, Florian Mertes, Laetitia Magnol, Caroline Chabert, Daniela Hartl, Yann Herault, Jean Maurice Delabar, Thomas Manke, Heinz Himmelbauer, and Joachim Klose, "Proteomic shifts in embryonic stem cells with gene dose modifications suggest the presence of balancer proteins in protein regulatory networks," PLoS One 2 (11), e1218-e1218 (2007).

Florian Mertes, Ojoplano – Identifizierung und Charakterisierung eines neuen Gens in Säugetieren sowie Etablierung einer konditionalen Knockout-Maus für Untersuchungen zur Funktion, PhD Thesis, Technische Universität, 2008.