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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.
We currently have no open PhD position.
We regularly recruit from the Life Science Zurich Graduate School PhD programs in Systems Biology and Systems Biology of Complex Diseases.
We always offer projects related to our research activities. Please consult the Research pages for a general overview and contact us directly.
For an overview of Master's theses previously done in our group see the Master's theses page.
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