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News
May 1
Our paper Reliable detection of subclonal
single-nucleotide variants in tumor cell populations appeared in Nature Communications today (see also ETH Life). In this work, we present the deepSNV algorithm and demonstrate its capability to detect subclonal mutations present in only 1/10,000 cells.
Gerstung et al. (2012) Nat Commun 3:811. DOI: 10.1038/ncomms1814.
| 16 May 2012 | Detecting tumour cells individually |
| 5-10 Jun 2011 | Ascona Workshop |
| 20 Nov 2010 | ETH Day: Golden Owl |
| 15 Jun 2009 | Abbott Swiss HIV Cohort Grant |
| 18 Apr 2009 | Algoritmen alom |
| 25 Apr 2008 | DNA jigsaw puzzle |
| 30 Nov 2007 | Computational Biology Workshop |
| 9 Nov 2007 | Computable cancer |
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