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Registered report: Melanoma genome sequencing reveals frequent PREX2 mutations

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 exp...

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Autores principales: Chroscinski, Denise, Sampey, Darryl, Hewitt, Alex, Iorns, Elizabeth, Gunn, William, Tan, Fraser, Lomax, Joelle, Errington, Timothy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4270141/
https://www.ncbi.nlm.nih.gov/pubmed/25490935
http://dx.doi.org/10.7554/eLife.04180
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author Chroscinski, Denise
Sampey, Darryl
Hewitt, Alex
Iorns, Elizabeth
Gunn, William
Tan, Fraser
Lomax, Joelle
Errington, Timothy
author_facet Chroscinski, Denise
Sampey, Darryl
Hewitt, Alex
Iorns, Elizabeth
Gunn, William
Tan, Fraser
Lomax, Joelle
Errington, Timothy
author_sort Chroscinski, Denise
collection PubMed
description 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 (Berger et al., 2012). 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; Berger et al., 2012). 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. DOI: http://dx.doi.org/10.7554/eLife.04180.001
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spelling pubmed-42701412015-01-29 Registered report: Melanoma genome sequencing reveals frequent PREX2 mutations Chroscinski, Denise Sampey, Darryl Hewitt, Alex Iorns, Elizabeth Gunn, William Tan, Fraser Lomax, Joelle Errington, Timothy eLife Cell Biology 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 (Berger et al., 2012). 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; Berger et al., 2012). 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. DOI: http://dx.doi.org/10.7554/eLife.04180.001 eLife Sciences Publications, Ltd 2014-12-10 /pmc/articles/PMC4270141/ /pubmed/25490935 http://dx.doi.org/10.7554/eLife.04180 Text en Copyright © 2014, Chroscinski et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Chroscinski, Denise
Sampey, Darryl
Hewitt, Alex
Iorns, Elizabeth
Gunn, William
Tan, Fraser
Lomax, Joelle
Errington, Timothy
Registered report: Melanoma genome sequencing reveals frequent PREX2 mutations
title Registered report: Melanoma genome sequencing reveals frequent PREX2 mutations
title_full Registered report: Melanoma genome sequencing reveals frequent PREX2 mutations
title_fullStr Registered report: Melanoma genome sequencing reveals frequent PREX2 mutations
title_full_unstemmed Registered report: Melanoma genome sequencing reveals frequent PREX2 mutations
title_short Registered report: Melanoma genome sequencing reveals frequent PREX2 mutations
title_sort registered report: melanoma genome sequencing reveals frequent prex2 mutations
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4270141/
https://www.ncbi.nlm.nih.gov/pubmed/25490935
http://dx.doi.org/10.7554/eLife.04180
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