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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
Nature, ISSN 0028-0836, 01/2017, Volume 541, Issue 7637, pp. 359 - 364
Journal Article
NATURE COMMUNICATIONS, ISSN 2041-1723, 01/2017, Volume 8, Issue 1, pp. 13671 - 13671
Journal Article
PLoS Genetics, ISSN 1553-7390, 11/2011, Volume 7, Issue 11
  In nature, stressful environments often occur in combination or close succession, and thus the ability to prepare for impending stress likely provides a... 
Proteins | Medical research | Yeast | Microbiology | Stress
Journal Article
Nucleic Acids Research, ISSN 0305-1048, 05/2010, Volume 38, Issue 13, pp. e142 - e142
Next-generation sequencing has proven an extremely effective technology for molecular counting applications where the number of sequence reads provides a... 
FITNESS | DESIGN | BIOACTIVE COMPOUNDS | SCREEN | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENES | LIBRARY | PRIMERS | YEAST GENOME | MODE-OF-ACTION | Mutation | Saccharomyces cerevisiae - genetics | Sequence Analysis, DNA - methods | Polymerase Chain Reaction | Methods Online
Journal Article
Science, ISSN 0036-8075, 2014, Volume 344, Issue 6180, pp. 208 - 211
Journal Article
Journal Article
Cell, ISSN 0092-8674, 05/2018, Volume 173, Issue 4, pp. 1003 - 1013.e15
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Journal Article