Related references
Note: Only part of the references are listed.Fast and SNP-tolerant detection of complex variants and splicing in short reads
Thomas D. Wu et al.
BIOINFORMATICS (2010)
Origins and functional impact of copy number variation in the human genome
Donald F. Conrad et al.
NATURE (2010)
Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing
Hansoo Park et al.
NATURE GENETICS (2010)
Copy Number Variation in Human Health, Disease, and Evolution
Feng Zhang et al.
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS (2009)
Sensitive and accurate detection of copy number variants using read depth of coverage
Seungtai Yoon 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)
Personalized copy number and segmental duplication maps using next-generation sequencing
Can Alkan et al.
NATURE GENETICS (2009)
High-resolution mapping of copy-number alterations with massively parallel sequencing
Derek Y. Chiang et al.
NATURE METHODS (2009)
The fine-scale and complex architecture of human copy-number variation
George H. Perry et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Copy number variation and evolution in humans and chimpanzees
George H. Perry et al.
GENOME RESEARCH (2008)
The complete genome of an individual by massively parallel DNA sequencing
David A. Wheeler et al.
NATURE (2008)
The diploid genome sequence of an Asian individual
Jun Wang et al.
NATURE (2008)
Accurate whole human genome sequencing using reversible terminator chemistry
David R. Bentley et al.
NATURE (2008)
The functional impact of structural variation in humans
Matthew E. Hurles et al.
TRENDS IN 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)
Challenges and standards in integrating surveys of structural variation
Stephen W. Scherer et al.
NATURE GENETICS (2007)
Methods and strategies for analyzing copy number variation using DNA microarrays
Nigel P. Carter
NATURE GENETICS (2007)
Global variation in copy number in the human genome
Richard Redon et al.
NATURE (2006)
Fine-scale structural variation of the human genome
E Tuzun et al.
NATURE GENETICS (2005)
Detection of large-scale variation in the human genome
AJ Iafrate et al.
NATURE GENETICS (2004)
Large-scale copy number polymorphism in the human genome
J Sebat et al.
SCIENCE (2004)
Representational oligonucleotide microarray analysis: A high-resolution method to detect genome copy number variation
R Lucito et al.
GENOME RESEARCH (2003)
Initial sequencing and analysis of the human genome
ES Lander et al.
NATURE (2001)
Share Paper
