Browsing Other ICR Research by author "Lise, Stefano"
Now showing items 1-2 of 2
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Identification of single nucleotide variants using position-specific error estimation in deep sequencing data
Kleftogiannis, D; Punta, M; Jayaram, A; Sandhu, S; Wong, S; et al. (2018-11-23)<h4>Background</h4> Targeted deep sequencing is a highly effective technology to identify known and novel single nucleotide variants (SNVs) with many applications in translational medicine, disease monitoring and cancer ... -
Identification of single nucleotide variants using position-specific error estimation in deep sequencing data.
Kleftogiannis, D; Punta, M; Jayaram, A; Sandhu, S; Wong, SQ; et al. (BMC, 2019-08-02)BACKGROUND: Targeted deep sequencing is a highly effective technology to identify known and novel single nucleotide variants (SNVs) with many applications in translational medicine, disease monitoring and cancer profiling. ...