Registered report: Melanoma genome sequencing reveals frequent PREX2 mutations

Author:

Chroscinski Denise1,Sampey Darryl2,Hewitt Alex3,

Affiliation:

1. Noble Life Sciences, Gaithersburg, United States

2. BioFactura, Frederick, United States

3. Department of Clinical Genetics, University of Melbourne, Melbourne, Australia

Abstract

The Reproducibility Project: Cancer Biology seeks to address growing concerns about reproducibility in scientific research by conducting replications of 50 papers in the field of cancer biology published between 2010 and 2012. This Registered Report describes the proposed replication plan of key experiments from ‘Melanoma genome sequencing reveals frequent PREX2 mutations’ by Berger and colleagues, published in Nature in 2012 (<xref ref-type="bibr" rid="bib1">Berger et al., 2012</xref>). The key experiments that will be replicated are those reported in Figure 3B and Supplementary Figure S6. In these experiments, Berger and colleagues show that somatic PREX2 mutations identified through whole-genome sequencing of human melanoma can contribute to enhanced lethality of tumor xenografts in nude mice (Figure 3B, S6B, and S6C; <xref ref-type="bibr" rid="bib1">Berger et al., 2012</xref>). The Reproducibility Project: Cancer Biology is a collaboration between the Center for Open Science and Science Exchange, and the results of the replications will be published by eLife.

Funder

Laura and John Arnold Foundation

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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