Integrated Genomic and Clinicopathologic Approach Distinguishes Pancreatic Grade 3 Neuroendocrine Tumor From Neuroendocrine Carcinoma and Identifies a Subset With Molecular Overlap

This publication has 48 references indexed in Scilit:

• Are G3 ENETS neuroendocrine neoplasms heterogeneous?
  Endocrine-Related Cancer, 2013
• DELLY: structural variant discovery by integrated paired-end and split-read analysis
  Bioinformatics, 2012
• Small Cell and Large Cell Neuroendocrine Carcinomas of the Pancreas are Genetically Similar and Distinct From Well-differentiated Pancreatic Neuroendocrine Tumors
  American Journal of Surgical Pathology, 2012
• A framework for variation discovery and genotyping using next-generation DNA sequencing data
  Nature Genetics, 2011
• DAXX / ATRX , MEN1 , and mTOR Pathway Genes Are Frequently Altered in Pancreatic Neuroendocrine Tumors
  Science, 2011
• A map of human genome variation from population-scale sequencing
  Nature, 2010
• The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
  Genome Research, 2010
• ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
  Nucleic Acids Research, 2010
• Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads
  Bioinformatics, 2009
• The Sequence Alignment/Map format and SAMtools
  Bioinformatics, 2009