Genome Fusion Detection: a novel method to detect fusion genes from SNP-array data
Published 2013 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Genome Fusion Detection: a novel method to detect fusion genes from SNP-array data
Authors
Keywords
-
Journal
BIOINFORMATICS
Volume 29, Issue 6, Pages 671-677
Publisher
Oxford University Press (OUP)
Online
2013-01-23
DOI
10.1093/bioinformatics/btt028
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Early landmark analysis of imatinib treatment in CML chronic phase: Less than 10% BCR-ABL by FISH at 3 months associated with improved long-term clinical outcome
- (2012) Lotta Ohm et al. AMERICAN JOURNAL OF HEMATOLOGY
- Overview of available methods for diverse RNA-Seq data analyses
- (2012) Geng Chen et al. Science China-Life Sciences
- Detection of Fused Genes in Eukaryotic Genomes using Gene deFuser: Analysis of the Tetrahymena thermophila genome
- (2011) Hannah MW Salim et al. BMC BIOINFORMATICS
- Detection of recurrent rearrangement breakpoints from copy number data
- (2011) Anna Ritz et al. BMC BIOINFORMATICS
- Lessons from a decade of integrating cancer copy number alterations with gene expression profiles
- (2011) N. Huang et al. BRIEFINGS IN BIOINFORMATICS
- Rapid High-Resolution Mapping of Balanced Chromosomal Rearrangements on Tiling CGH Arrays
- (2011) Harvey A. Greisman et al. JOURNAL OF MOLECULAR DIAGNOSTICS
- Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants
- (2011) Dalila Pinto et al. NATURE BIOTECHNOLOGY
- Evidence for compensatory upregulation of expressed X-linked genes in mammals, Caenorhabditis elegans and Drosophila melanogaster
- (2011) Xinxian Deng et al. NATURE GENETICS
- deFuse: An Algorithm for Gene Fusion Discovery in Tumor RNA-Seq Data
- (2011) Andrew McPherson et al. PLoS Computational Biology
- The potential for crizotinib in non-small cell lung cancer: a perspective review
- (2011) Yung-Jue Bang Therapeutic Advances in Medical Oncology
- Conditional random pattern model for copy number aberration detection
- (2010) Fuhai Li et al. BMC BIOINFORMATICS
- Distinct Genomic Alterations in Prostate Cancers in Chinese and Western Populations Suggest Alternative Pathways of Prostate Carcinogenesis
- (2010) X. Mao et al. CANCER RESEARCH
- Detection of DNA fusion junctions for BCR-ABL translocations by Anchored ChromPET
- (2010) Yoshiyuki Shibata et al. Genome Medicine
- PICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer data
- (2009) C. D. Greenman et al. BIOSTATISTICS
- Sorafenib Induces Apoptosis Specifically in Cells Expressing BCR/ABL by Inhibiting Its Kinase Activity to Activate the Intrinsic Mitochondrial Pathway
- (2009) T. Kurosu et al. CANCER RESEARCH
- Next-generation DNA sequencing of paired-end tags (PET) for transcriptome and genome analyses
- (2009) M. J. Fullwood et al. GENOME RESEARCH
- Transcriptome sequencing to detect gene fusions in cancer
- (2009) Christopher A. Maher et al. NATURE
- Origins and functional impact of copy number variation in the human genome
- (2009) Donald F. Conrad et al. NATURE
- The Fine-Scale and Complex Architecture of Human Copy-Number Variation
- (2008) George H. Perry et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs
- (2008) Joshua M Korn et al. NATURE GENETICS
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started