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by Alioto, Tyler S and Buchhalter, Ivo and Derdak, Sophia and Hutter, Barbara and Eldridge, Matthew D and Hovig, Eivind and Heisler, Lawrence E and Beck, Timothy A and Simpson, Jared T and Tonon, Laurie and Sertier, Anne-Sophie and Patch, Ann-Marie and Jäger, Natalie and Ginsbach, Philip and Drews, Ruben and Paramasivam, Nagarajan and Kabbe, Rolf and Chotewutmontri, Sasithorn and Diessl, Nicolle and Previti, Christopher and Schmidt, Sabine and Brors, Benedikt and Feuerbach, Lars and Heinold, Michael and Gröbner, Susanne and Korshunov, Andrey and Tarpey, Patrick S and Butler, Adam P and Hinton, Jonathan and Jones, David and Menzies, Andrew and Raine, Keiran and Shepherd, Rebecca and Stebbings, Lucy and Teague, Jon W and Ribeca, Paolo and Giner, Francesc Castro and Beltran, Sergi and Raineri, Emanuele and Dabad, Marc and Heath, Simon C and Gut, Marta and Denroche, Robert E and Harding, Nicholas J and Yamaguchi, Takafumi N and Fujimoto, Akihiro and Nakagawa, Hidewaki and Quesada, Víctor and Valdés-Mas, Rafael and Nakken, Sigve and Vodák, Daniel and Bower, Lawrence and Lynch, Andrew G and Anderson, Charlotte L and Waddell, Nicola and Pearson, John V and Grimmond, Sean M and Peto, Myron and Spellman, Paul and He, Minghui and Kandoth, Cyriac and Lee, Semin and Zhang, John and Létourneau, Louis and Ma, Singer and Seth, Sahil and Torrents, David and Xi, Liu and Wheeler, David A and López-Otín, Carlos and Campo, Elías and Campbell, Peter J and Boutros, Paul C and Puente, Xose S and Gerhard, Daniela S and Pfister, Stefan M and McPherson, John D and Hudson, Thomas J and Schlesner, Matthias and Lichter, Peter and Eils, Roland and Jones, David T.W and Gut, Ivo G
Nature Communications, ISSN 2041-1723, 12/2015, Volume 6, Issue 1, p. 10001
As whole-genome sequencing for cancer genome analysis becomes a clinical tool, a full understanding of the variables affecting sequencing analysis output is... 
POINT MUTATIONS | EXOME | ACCURATE | VARIANT ANALYSIS | SIGNATURES | ALIGNMENT | MULTIDISCIPLINARY SCIENCES | FRAMEWORK | Mutation | Genome, Human | High-Throughput Nucleotide Sequencing - methods | Medulloblastoma - genetics | Humans | Leukemia, Lymphoid - genetics | Càncer | Medical genetics | Mutació (Biologia) | Genètica mèdica | Genètica humana | Human genetics | Mutation (Biology) | Cancer
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 5307 - 6
Sample pooling enabled by dedicated indexes is a common strategy for cost-effective and robust high-throughput sequencing. Index misassignment leading to... 
FRAMEWORK | MUTATIONS | GENOME ANALYSIS | CANCER | MULTIDISCIPLINARY SCIENCES | Next-generation sequencing | Contamination | Tumors | Cancer
Journal Article
Cell Reports, ISSN 2211-1247, 06/2017, Volume 19, Issue 10, pp. 2045 - 2059
Journal Article
Bioinformatics, ISSN 1367-4803, 05/2018, Volume 34, Issue 10, pp. 1778 - 1780
Abstract Summary Individual tumor genomes pose a major challenge for clinical interpretation due to their unique sets of acquired mutations. There is a general... 
BIOTECHNOLOGY & APPLIED MICROBIOLOGY | ANNOTATION | BIOCHEMICAL RESEARCH METHODS | MATHEMATICAL & COMPUTATIONAL BIOLOGY | GENETIC-VARIANTS | MUTATIONS | TOOL | Applications Notes
Journal Article
Journal Article
Applied Optics, ISSN 1559-128X, 09/2014, Volume 53, Issue 25, pp. 5606 - 5613
Epitaxial ZnSe thin films exhibiting two important defects, i.e., boundary roughness and thickness nonuniformity, prepared on GaAs substrates, are optically... 
LARGE-AREA | DEPOLARIZATION | BOUNDARIES | CHEMICAL-VAPOR-DEPOSITION | SUM-RULE | LIGHT-SCATTERING | DOUBLE-LAYERS | OPTICS | SURFACE-ROUGHNESS | II-VI COMPOUNDS | SPECTROSCOPIC ELLIPSOMETRY | Thin films | Atomic force microscopy | Usage | Optical properties | Matrices | Dielectric films | Reflectometer | Ellipsometry | Spectroscopy | Roughness | Zinc selenides | Constants | Mathematical models | Boundaries | Nonuniformity | Standards
Journal Article