Lista de obras -

A landscape of driver mutations in melanoma

artículo científico publicado en 2012

A pan-cancer analysis of transcriptome changes associated with somatic mutations in U2AF1 reveals commonly altered splicing events

artículo científico publicado en 2014

Comparative analysis of RNA sequencing methods for degraded or low-input samples

artículo científico publicado en 2013

Complementary genomic approaches highlight the PI3K/mTOR pathway as a common vulnerability in osteosarcoma

artículo científico publicado en 2014

Evolution and impact of subclonal mutations in chronic lymphocytic leukemia

artículo científico publicado en 2013

Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity

artículo científico publicado en 2013

Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer

artículo científico publicado en 2012

Genome-scale DNA methylation maps of pluripotent and differentiated cells

artículo científico publicado en 2008

Genomic sequencing of colorectal adenocarcinomas identifies a recurrent VTI1A-TCF7L2 fusion

artículo científico publicado en 2011

Inhibitor-sensitive FGFR2 and FGFR3 mutations in lung squamous cell carcinoma

artículo científico publicado en 2013

Initial genome sequencing and analysis of multiple myeloma

artículo científico publicado en 2011

Integrative analysis of the melanoma transcriptome

artículo científico publicado en 2010

Mapping the hallmarks of lung adenocarcinoma with massively parallel sequencing

artículo científico publicado en 2012

Massively parallel sequencing of human urinary exosome/microvesicle RNA reveals a predominance of non-coding RNA.

artículo científico publicado en 2014

Medulloblastoma exome sequencing uncovers subtype-specific somatic mutations

artículo científico publicado en 2012

Mutational heterogeneity in cancer and the search for new cancer-associated genes

artículo científico publicado en 2013

PRADA: pipeline for RNA sequencing data analysis

artículo científico publicado en 2014

Punctuated evolution of prostate cancer genomes

artículo científico publicado en 2013

RNA-SeQC: RNA-seq metrics for quality control and process optimization

artículo científico publicado en 2012

RNA-Seq methods for imperfect samples: development, evaluation and applications

artículo científico publicado en 2011

SF3B1 and other novel cancer genes in chronic lymphocytic leukemia

artículo científico publicado en 2011

Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples

artículo científico publicado en 2013

Somatic mutation of CDKN1B in small intestine neuroendocrine tumors

artículo científico publicado en 2013

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

artículo científico publicado en 2010

The genetic landscape of high-risk neuroblastoma

artículo científico publicado en 2013

The genomic landscape of pediatric Ewing sarcoma

artículo científico publicado en 2014

Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine

artículo científico publicado en 2014

Lista de obras de

A landscape of driver mutations in melanoma

A pan-cancer analysis of transcriptome changes associated with somatic mutations in U2AF1 reveals commonly altered splicing events

Comparative analysis of RNA sequencing methods for degraded or low-input samples

Complementary genomic approaches highlight the PI3K/mTOR pathway as a common vulnerability in osteosarcoma

Evolution and impact of subclonal mutations in chronic lymphocytic leukemia

Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity

Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer

Genome-scale DNA methylation maps of pluripotent and differentiated cells

Genomic sequencing of colorectal adenocarcinomas identifies a recurrent VTI1A-TCF7L2 fusion

Inhibitor-sensitive FGFR2 and FGFR3 mutations in lung squamous cell carcinoma

Initial genome sequencing and analysis of multiple myeloma

Integrative analysis of the melanoma transcriptome

Mapping the hallmarks of lung adenocarcinoma with massively parallel sequencing

Massively parallel sequencing of human urinary exosome/microvesicle RNA reveals a predominance of non-coding RNA.

Medulloblastoma exome sequencing uncovers subtype-specific somatic mutations

Mutational heterogeneity in cancer and the search for new cancer-associated genes

PRADA: pipeline for RNA sequencing data analysis

Punctuated evolution of prostate cancer genomes

RNA-SeQC: RNA-seq metrics for quality control and process optimization

RNA-Seq methods for imperfect samples: development, evaluation and applications

SF3B1 and other novel cancer genes in chronic lymphocytic leukemia

Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples

Somatic mutation of CDKN1B in small intestine neuroendocrine tumors

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

The genetic landscape of high-risk neuroblastoma

The genomic landscape of pediatric Ewing sarcoma

Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine