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Methods

Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding

  • Kevin Judd McKernan
  • Heather E. Peckham
  • Gina L. Costa
  • Stephen F. McLaughlin
  • Yutao Fu
  • Eric F. Tsung Christopher R. Clouser Cisyla Duncan Jeffrey K. Ichikawa Clarence C. Lee Zheng Zhang Swati S. Ranade Eileen T. Dimalanta Fiona C. Hyland Tanya D. Sokolsky Lei Zhang Andrew Sheridan Haoning Fu Cynthia L. Hendrickson Bin Li Lev Kotler Jeremy R. Stuart Joel A. Malek Jonathan M. Manning Alena A. Antipova Damon S. Perez Michael P. Moore Kathleen C. Hayashibara Michael R. Lyons Robert E. Beaudoin Brittany E. Coleman Michael W. Laptewicz Adam E. Sannicandro Michael D. Rhodes Rajesh K. Gottimukkala Shan Yang Vineet Bafna Ali Bashir Andrew MacBride Can Alkan Jeffrey M. Kidd
  • ... [+36 authors] ...,
  • Evan E. Eichler
  • Martin G. Reese
  • Francisco M. De La Vega
  • Alan P. Blanchard
  • First Published June 22, 2009
Methods

A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease

  • Heather C. Mefford
  • Gregory M. Cooper
  • Troy Zerr
  • Joshua D. Smith
  • Carl Baker
  • Neil Shafer Erik C. Thorland
  • ... [+2 authors] ...,
  • Cindy Skinner
  • Charles E. Schwartz
  • Deborah A. Nickerson
  • Evan E. Eichler
  • First Published June 8, 2009
Methods

Combinatorial algorithms for structural variation detection in high-throughput sequenced genomes

  • Fereydoun Hormozdiari
  • Can Alkan
  • Evan E. Eichler
  • S. Cenk Sahinalp
  • First Published May 15, 2009
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