Identifying gene disruptions in novel balanced de novo constitutional translocations in childhood cancer patients by whole-genome sequencing
- 1 October 2015
- journal article
- research article
- Published by Elsevier in Genetics in Medicine
- Vol. 17 (10) , 831-835
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Comprehensive molecular characterization of human colon and rectal cancerNature, 2012
- DCC constrains tumour progression via its dependence receptor activityNature, 2011
- CREST maps somatic structural variation in cancer genomes with base-pair resolutionNature Methods, 2011
- deFuse: An Algorithm for Gene Fusion Discovery in Tumor RNA-Seq DataPLOS Computational Biology, 2011
- Novel roles for Slits and netrins: axon guidance cues as anticancer targets?Nature Reviews Cancer, 2011
- Whole-Genome Sequencing in a Patient with Charcot–Marie–Tooth NeuropathyNew England Journal of Medicine, 2010
- MiR-218 Inhibits Invasion and Metastasis of Gastric Cancer by Targeting the Robo1 ReceptorPLOS Genetics, 2010
- BreakDancer: an algorithm for high-resolution mapping of genomic structural variationNature Methods, 2009
- High-Throughput Multiplex Sequencing to Discover Copy Number Variants in DrosophilaGenetics, 2009
- MODY-like diabetes associated with an apparently balanced translocation: possible involvement of MPP7 gene and cell polarity in the pathogenesis of diabetesMolecular Cytogenetics, 2009