Copy number changes of clinically actionable genes in melanoma, non-small cell lung cancer and colorectal cancer-A survey across 822 routine diagnostic cases

Distinctive Spatiotemporal Stability of Somatic Mutations in Metastasized Microsatellite-stable Colorectal Cancer

(2015) Moritz Jesinghaus et al.   AMERICAN JOURNAL OF SURGICAL PATHOLOGY

Genomic Classification of Cutaneous Melanoma

(2015) Rehan Akbani et al.   CELL

Genetic heterogeneity in synchronous colorectal cancers impacts genotyping approaches and therapeutic strategies

(2015) Moritz Jesinghaus et al.   GENES CHROMOSOMES & CANCER

Mutations in genes encoding PI3K-AKT and MAPK signaling define anogenital papillary hidradenoma

(2015) Nicole Pfarr et al.   GENES CHROMOSOMES & CANCER

High-throughput diagnostic profiling of clinically actionable gene fusions in lung cancer

(2015) Nicole Pfarr et al.   GENES CHROMOSOMES & CANCER

Activating PIK3CA mutations coexist with BRAF or NRAS mutations in a limited fraction of melanomas

(2015) Antonella Manca et al.   Journal of Translational Medicine

A copy number variation map of the human genome

(2015) Mehdi Zarrei et al.   NATURE REVIEWS GENETICS

Somatic gene copy number alterations in colorectal cancer: new quest for cancer drivers and biomarkers

(2015) H Wang et al.   ONCOGENE

Semiconductor-Based Sequencing of Formalin-Fixed, Paraffin-Embedded Colorectal Cancer Samples

(2015) A. Stenzinger et al.   ONCOLOGIST

Computational methods for detecting copy number variations in cancer genome using next generation sequencing: principles and challenges

(2015) Biao Liu et al.   Oncotarget

Targeted ultra-deep sequencing reveals recurrent and mutually exclusive mutations of cancer genes in blastic plasmacytoid dendritic cell neoplasm

(2015) Albrecht Stenzinger et al.   Oncotarget

The Molecular Pathology of Melanoma: An Integrated Taxonomy of Melanocytic Neoplasia

(2014) Boris C. Bastian   Annual Review of Pathology-Mechanisms of Disease

Copy number variation detection using next generation sequencing read counts

(2014) Heng Wang et al.   BMC BIOINFORMATICS

Clinical massively parallel next-generation sequencing analysis of 409 cancer-related genes for mutations and copy number variations in solid tumours

(2014) R R Singh et al.   BRITISH JOURNAL OF CANCER

Copy number variants in clinical next-generation sequencing data can define the relationship between simultaneous tumors in an individual patient

(2014) Jennifer K. Sehn et al.   EXPERIMENTAL AND MOLECULAR PATHOLOGY

COSMIC: exploring the world's knowledge of somatic mutations in human cancer

(2014) Simon A. Forbes et al.   NUCLEIC ACIDS RESEARCH

Identification of Druggable Cancer Driver Genes Amplified across TCGA Datasets

(2014) Ying Chen et al.   PLoS One

High-Throughput Sequencing and Copy Number Variation Detection Using Formalin Fixed Embedded Tissue in Metastatic Gastric Cancer

(2014) Seokhwi Kim et al.   PLoS One

Molecular Diagnostic Profiling of Lung Cancer Specimens with a Semiconductor-Based Massive Parallel Sequencing Approach

(2013) Volker Endris et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Pan-cancer patterns of somatic copy number alteration

(2013) Travis I Zack et al.   NATURE GENETICS

Detection of structural DNA variation from next generation sequencing data: a review of informatic approaches

(2013) Haley J. Abel et al.   Cancer Genetics

Functional genomic analysis of chromosomal aberrations in a compendium of 8000 cancer genomes

(2012) T.-M. Kim et al.   GENOME RESEARCH

Quantitative Analysis of Diagnostic Guidelines for HER2-Status Assessment

(2012) Albrecht Stenzinger et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Accurate and exact CNV identification from targeted high-throughput sequence data

(2011) Alex S Nord et al.   BMC GENOMICS

Amplification of the PDGFRA, KIT and KDR genes in glioblastoma: a population-based study

(2011) Sumihito Nobusawa et al.   NEUROPATHOLOGY

BRAF Gene Amplification Can Promote Acquired Resistance to MEK Inhibitors in Cancer Cells Harboring the BRAF V600E Mutation

(2010) R. B. Corcoran et al.   Science Signaling

Gene copy number variation and common human disease

(2009) M Fanciulli et al.   CLINICAL GENETICS

Origins and functional impact of copy number variation in the human genome

(2009) Donald F. Conrad et al.   NATURE

Copy number variations and cancer

(2009) Adam Shlien et al.   Genome Medicine

Functional Copy-Number Alterations in Cancer

(2008) Barry S. Taylor et al.   PLoS One