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
