Troy Zerr

发表

Mapping and sequencing of structural variation from eight human genomes

Joshua M. Korn, Nancy F. Hansen, D. Altshuler, 2008, Nature.

Systematic assessment of copy number variant detection via genome-wide SNP genotyping

E. Eichler, D. Nickerson, J. Kidd, 2008, Nature Genetics.

Automated band mapping in electrophoretic gel images using background information

S. Henikoff, Troy Zerr, 2005, Nucleic acids research.

High-throughput discovery of rare human nucleotide polymorphisms by Ecotilling

S. Henikoff, Troy Zerr, E. A. Greene, 2006, Nucleic acids research.

A protocol for TILLING and Ecotilling in plants and animals

S. Henikoff, Troy Zerr, L. Comai, 2006, Nature Protocols.

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

H. Mefford, E. Eichler, C. Alkan, 2009 .

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

Deborah A Nickerson, Gregory M Cooper, Carl Baker, 2009, Genome research.

Targeted interrogation of copy number variation using SCIMMkit

Gregory M. Cooper, Deborah A. Nickerson, Evan E. Eichler, 2009, Bioinform..

A protocol for TILLING and eco-TILLING.

S. Henikoff, Troy Zerr, L. Comai, 2012 .

Systematic assessment of copy-number variant detection via genome-wide single nucleotide polymorphism genotyping

E. Eichler, D. Nickerson, J. Kidd, 2009 .