NGS panel V1.1 for the routine deep sequencing-based diagnostic of somatic hotspot theranostic mutations on FFPE tumours: A prospective study of 500 cancer samples - Archive ouverte HAL Access content directly
Conference Papers European Journal of Cancer Year : 2013

NGS panel V1.1 for the routine deep sequencing-based diagnostic of somatic hotspot theranostic mutations on FFPE tumours: A prospective study of 500 cancer samples

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Life Sciences [q-bio] Cancer

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https://hal-univ-rennes1.archives-ouvertes.fr/hal-00935121

Submitted on : Thursday, January 23, 2014-10:24:05 AM

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hal-00935121 , version 1 (23-01-2014)

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  • HAL Id : hal-00935121 , version 1

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A. Lespagnol, B. Ndiaye, Annick Mosser, C. Chaplais, H. Gourdet, et al.. NGS panel V1.1 for the routine deep sequencing-based diagnostic of somatic hotspot theranostic mutations on FFPE tumours: A prospective study of 500 cancer samples. 17th ECCO / 38th ESMO / 32nd ESTRO European Cancer Congress on Reinforcing Multidisciplinarity, Sep 2013, Amsterdam, Netherlands. pp.S200-S200. ⟨hal-00935121⟩

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