An open access pilot freely sharing cancer genomic data from participants in Texas

Acquire: an open-source comprehensive cancer biobanking system

(2015) H. Dowst et al.   BIOINFORMATICS

Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline

(2014) Jeffrey G Reid et al.   BMC BIOINFORMATICS

Biobanking 3.0: Evidence based and customer focused biobanking

(2014) Daniel Simeon-Dubach et al.   CLINICAL BIOCHEMISTRY

Genomic cloud computing: legal and ethical points to consider

(2014) Edward S Dove et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

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

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

Detection of a Recurrent DNAJB1-PRKACA Chimeric Transcript in Fibrolamellar Hepatocellular Carcinoma

(2014) J. N. Honeyman et al.   SCIENCE

Open Access Data Sharing in Genomic Research

(2014) Stacey Pereira et al.   Genes

Participants' Recall and Understanding of Genomic Research and Large-Scale Data Sharing

(2013) Jill Oliver Robinson et al.   Journal of Empirical Research on Human Research Ethics

Comprehensive molecular characterization of clear cell renal cell carcinoma

(2013)   NATURE

Identifying Personal Genomes by Surname Inference

(2013) M. Gymrek et al.   SCIENCE

The Complexities of Genomic Identifiability

(2013) L. L. Rodriguez et al.   SCIENCE

An integrative variant analysis suite for whole exome next-generation sequencing data

(2012) Danny Challis et al.   BMC BIOINFORMATICS

Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes

(2012) Andrew V. Biankin et al.   NATURE

qpure: A Tool to Estimate Tumor Cellularity from Genome-Wide Single-Nucleotide Polymorphism Profiles

(2012) Sarah Song et al.   PLoS One

A public resource facilitating clinical use of genomes

(2012) Madeleine P. Ball et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Charting a course for genomic medicine from base pairs to bedside

(2011) Eric D. Green et al.   NATURE

Targeted enrichment beyond the consensus coding DNA sequence exome reveals exons with higher variant densities

(2011) Matthew N Bainbridge et al.   GENOME BIOLOGY

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

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

Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads

(2009) K. Ye et al.   BIOINFORMATICS

A SNP discovery method to assess variant allele probability from next-generation resequencing data

(2009) Y. Shen et al.   GENOME RESEARCH

Resolving Individuals Contributing Trace Amounts of DNA to Highly Complex Mixtures Using High-Density SNP Genotyping Microarrays

(2008) Nils Homer et al.   PLoS Genetics