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Archives of Disease in Childhood. Fetal and Neonatal Edition, ISSN 1359-2998, 12/2013, Volume 98, Issue 12, p. S236
Journal Article
Archives of disease in childhood - Education & practice edition, ISSN 1743-0585, 12/2013, Volume 98, Issue 6, pp. 236 - 238
Next generation sequencing (NGS), massively parallel or deep sequencing are related terms that describe a DNA sequencing technology which has revolutionised... 
Basic Science | PEDIATRICS | Technology | DNA | Genomics - instrumentation | Pediatrics | Humans | Mutation | Genome, Human | High-Throughput Nucleotide Sequencing - methods | Sequence Analysis, DNA - methods | Research in Practice | 1506
Journal Article
Cell, ISSN 0092-8674, 05/2012, Volume 149, Issue 5, pp. 979 - 993
Journal Article
Nature Genetics, ISSN 1061-4036, 12/2013, Volume 45, Issue 12, pp. 1479 - 1482
Journal Article
Cell, ISSN 0092-8674, 05/2012, Volume 149, Issue 5, pp. 994 - 1007
Journal Article
Nature, ISSN 0028-0836, 2012, Volume 486, Issue 7403, pp. 400 - +
Journal Article
Nature, ISSN 0028-0836, 09/2014, Volume 513, Issue 7518, pp. 422 - 5
Journal Article
Nature, ISSN 0028-0836, 01/2010, Volume 463, Issue 7279, pp. 360 - 363
Journal Article
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 Genetics, ISSN 1061-4036, 02/2015, Volume 47, Issue 3, pp. 257 - 262
Journal Article