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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

  • First Published June 22, 2009
Methods

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

  • First Published June 8, 2009
Methods

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

  • First Published May 15, 2009
Methods

Physical map-assisted whole-genome shotgun sequence assemblies

  • First Published June 1, 2006
Methods

Mapping segmental and sequence variations among laboratory mice using BAC array CGH

  • First Published February 1, 2005
Methods

Assessment of SAGE in Transcript Identification

  • First Published May 12, 2003
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