Germline and somatic mutation profile in Cancer patients revealed by a medium-sized pan-Cancer panel

Molecular profiling for precision cancer therapies

(2020) Eoghan R. Malone et al.   Genome Medicine

SnapShot: TCGA-Analyzed Tumors

(2018) Amy Blum et al.   CELL

Tearing down the walls: FDA approves next generation sequencing (NGS) assays for actionable cancer genomic aberrations

(2018) Matteo Allegretti et al.   JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH

Analytical Validation of a Hybrid Capture–Based Next-Generation Sequencing Clinical Assay for Genomic Profiling of Cell-Free Circulating Tumor DNA

(2018) Travis A. Clark et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries

(2018) Freddie Bray et al.   CA-A CANCER JOURNAL FOR CLINICIANS

COSMIC: the Catalogue Of Somatic Mutations In Cancer

(2018) John G Tate et al.   NUCLEIC ACIDS RESEARCH

Analysis of 100,000 human cancer genomes reveals the landscape of tumor mutational burden

(2017) Zachary R. Chalmers et al.   Genome Medicine

Exploring cancer genomic data from the cancer genome atlas project

(2016) Ju-Seog Lee   BMB Reports

Evaluating the necessity of PCR duplicate removal from next-generation sequencing data and a comparison of approaches

(2016) Mark T. W. Ebbert et al.   BMC BIOINFORMATICS

Cancer statistics in China, 2015

(2016) Wanqing Chen et al.   CA-A CANCER JOURNAL FOR CLINICIANS

A global reference for human genetic variation

(2015) Richard A. Gibbs et al.   NATURE

Acquired EGFR C797S mutation mediates resistance to AZD9291 in non–small cell lung cancer harboring EGFR T790M

(2015) Kenneth S Thress et al.   NATURE MEDICINE

ClinVar: public archive of interpretations of clinically relevant variants

(2015) Melissa J. Landrum et al.   NUCLEIC ACIDS RESEARCH

Global cancer transitions according to the Human Development Index (2008–2030): a population-based study

(2012) Freddie Bray et al.   LANCET ONCOLOGY

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

(2010) A. McKenna et al.   GENOME RESEARCH

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

(2010) K. Wang et al.   NUCLEIC ACIDS RESEARCH

Fast and accurate short read alignment with Burrows-Wheeler transform

(2009) H. Li et al.   BIOINFORMATICS