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Method

Alu/Alu-mediated rearrangements" > Predicting human genes susceptible to genomic instability associated with Alu/Alu-mediated rearrangements

  • First Published June 15, 2018
Method

Optimizing sparse sequencing of single cells for highly multiplex copy number profiling

  • First Published April 9, 2015
Research

Deletions of recessive disease genes: CNV contribution to carrier states and disease-causing alleles

  • First Published May 16, 2013
Research

NAHR-mediated copy-number variants in a clinical population: Mechanistic insights into both genomic disorders and Mendelizing traits

  • First Published May 8, 2013
Research

Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes

  • First Published January 4, 2011
Methods

Inferring tumor progression from genomic heterogeneity

  • First Published November 10, 2009
LETTER

Copy number variation at the breakpoint region of isochromosome 17q

  • First Published August 19, 2008
LETTER

AT-rich repeats associated with chromosome 22q11.2 rearrangement disorders shape human genome architecture on Yq12

  • First Published February 6, 2007
LETTER

Novel patterns of genome rearrangement and their association with survival in breast cancer

  • First Published December 1, 2006
ARTICLE

Serial segmental duplications during primate evolution result in complex human genome architecture

  • First Published November 1, 2004
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