Related references
Note: Only part of the references are listed.Massive Genomic Rearrangement Acquired in a Single Catastrophic Event during Cancer Development
Philip J. Stephens et al.
CELL (2011)
Chromosome Catastrophes Involve Replication Mechanisms Generating Complex Genomic Rearrangements
Pengfei Liu et al.
CELL (2011)
Dindel: Accurate indel calls from short-read data
Cornelis A. Albers et al.
GENOME RESEARCH (2011)
Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis
Ivonne Jarick et al.
HUMAN MOLECULAR GENETICS (2011)
Sequence-based characterization of structural variation in the mouse genome
Binnaz Yalcin et al.
NATURE (2011)
Mapping copy number variation by population-scale genome sequencing
Ryan E. Mills et al.
NATURE (2011)
The genomic complexity of primary human prostate cancer
Michael F. Berger et al.
NATURE (2011)
Mouse genomic variation and its effect on phenotypes and gene regulation
Thomas M. Keane et al.
NATURE (2011)
APPLICATIONS OF NEXT-GENERATION SEQUENCING Genome structural variation discovery and genotyping
Can Alkan et al.
NATURE REVIEWS GENETICS (2011)
Break-Induced Replication Is Highly Inaccurate
Angela Deem et al.
PLOS BIOLOGY (2011)
Copy number variant detection in inbred strains from short read sequence data
Jared T. Simpson et al.
BIOINFORMATICS (2010)
A Human Genome Structural Variation Sequencing Resource Reveals Insights into Mutational Mechanisms
Jeffrey M. Kidd et al.
CELL (2010)
De novo rates and selection of large copy number variation
Andy Itsara et al.
GENOME RESEARCH (2010)
Genome-wide mapping and assembly of structural variant breakpoints in the mouse genome
Aaron R. Quinlan et al.
GENOME RESEARCH (2010)
Large, rare chromosomal deletions associated with severe early-onset obesity
Elena G. Bochukova et al.
NATURE (2010)
Origins and functional impact of copy number variation in the human genome
Donald F. Conrad et al.
NATURE (2010)
Functional impact of global rare copy number variation in autism spectrum disorders
Dalila Pinto et al.
NATURE (2010)
Mutation spectrum revealed by breakpoint sequencing of human germline CNVs
Donald F. Conrad et al.
NATURE GENETICS (2010)
Diversity of Human Copy Number Variation and Multicopy Genes
Peter H. Sudmant et al.
SCIENCE (2010)
Enhanced structural variant and breakpoint detection using SVMerge by integration of multiple detection methods and local assembly
Kim Wong et al.
GENOME BIOLOGY (2010)
Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads
Kai Ye et al.
BIOINFORMATICS (2009)
LookSeq: A browser-based viewer for deep sequencing data
Heinrich Magnus Manske et al.
GENOME RESEARCH (2009)
Mapping and sequencing of structural variation from eight human genomes (Reprinted from Nature, vol 453, pg 56-64, 2008)
Jeffrey M. Kidd et al.
NATURE GENETICS (2009)
Copy number variation at 1q21.1 associated with neuroblastoma
Sharon J. Diskin et al.
NATURE (2009)
The DNA replication FoSTeS/MMBIR mechanism can generate genomic, genic and exonic complex rearrangements in humans
Feng Zhang et al.
NATURE GENETICS (2009)
Computational methods for discovering structural variation with next-generation sequencing
Paul Medvedev et al.
NATURE METHODS (2009)
BreakDancer: an algorithm for high-resolution mapping of genomic structural variation
Ken Chen et al.
NATURE METHODS (2009)
Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans
Bin Xu et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Extending genome-wide association studies to copy-number variation
Steven A. McCarroll
HUMAN MOLECULAR GENETICS (2008)
Mapping and sequencing of structural variation from eight human genomes
Jeffrey M. Kidd et al.
NATURE (2008)
Paired-end mapping reveals extensive structural variation in the human genome
Jan O. Korbel et al.
SCIENCE (2007)
Copy-number variation and association studies of human disease
Steven A. McCarroll et al.
NATURE GENETICS (2007)
Global variation in copy number in the human genome
Richard Redon et al.
NATURE (2006)
Genome-wide genetic association of complex traits in heterogeneous stock mice
William Valdar et al.
NATURE GENETICS (2006)
Genetic dissection of a behavioral quantitative trait locus shows that Rgs2 modulates anxiety in mice
B Yalcin et al.
NATURE GENETICS (2004)
Shotgun sequence assembly and recent segmental duplications within the human genome
XW She et al.
NATURE (2004)
DNA repair mediated by endonuclease-independent LINE-1 retrotransposition
TA Morrish et al.
NATURE GENETICS (2002)