Search Results - "Zerr, Troy"

Systematic assessment of copy number variant detection via genome-wide SNP genotyping by Cooper, Gregory M, Zerr, Troy, Kidd, Jeffrey M, Eichler, Evan E, Nickerson, Deborah A

“…SNP genotyping has emerged as a technology to incorporate copy number variants (CNVs) into genetic analyses of human traits. However, the extent to which SNP…”
Get full text

A protocol for TILLING and Ecotilling in plants and animals by Henikoff, Steven, Till, Bradley J, Zerr, Troy, Comai, Luca

“…We describe Targeting-Induced Local Lesions IN Genomes (TILLING), a reverse-genetic strategy for the discovery and mapping of induced mutations. TILLING is…”
Get full text

Mapping and sequencing of structural variation from eight human genomes by Eichler, Evan E, Kidd, Jeffrey M, Cooper, Gregory M, Donahue, William F, Hayden, Hillary S, Sampas, Nick, Graves, Tina, Hansen, Nancy, Teague, Brian, Alkan, Can, Antonacci, Francesca, Haugen, Eric, Zerr, Troy, Yamada, N. Alice, Tsang, Peter, Newman, Tera L, Tüzün, Eray, Cheng, Ze, Ebling, Heather M, Tusneem, Nadeem, David, Robert, Gillett, Will, Phelps, Karen A, Weaver, Molly, Saranga, David, Brand, Adrianne, Tao, Wei, Gustafson, Erik, McKernan, Kevin, Chen, Lin, Malig, Maika, Smith, Joshua D, Korn, Joshua M, McCarroll, Steven A, Altshuler, David A, Peiffer, Daniel A, Dorschner, Michael, Stamatoyannopoulos, John, Schwartz, David, Nickerson, Deborah A, Mullikin, James C, Wilson, Richard K, Bruhn, Laurakay, Olson, Maynard V, Kaul, Rajinder, Smith, Douglas R

“…Genetic variation among individual humans occurs on many different scales, ranging from gross alterations in the human karyotype to single nucleotide changes…”
Get full text

A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease by Mefford, Heather C, Cooper, Gregory M, Zerr, Troy, Smith, Joshua D, Baker, Carl, Shafer, Neil, Thorland, Erik C, Skinner, Cindy, Schwartz, Charles E, Nickerson, Deborah A, Eichler, Evan E

“…Copy-number variants (CNVs) are substantial contributors to human disease. A central challenge in CNV-disease association studies is to characterize the…”
Get full text

Automated band mapping in electrophoretic gel images using background information by Zerr, Troy, Henikoff, Steven

“…Some popular methods for polymorphism and mutation discovery involve ascertainment of novel bands by the examination of electrophoretic gel images. Although…”
Get full text

High-throughput discovery of rare human nucleotide polymorphisms by Ecotilling by Till, Bradley J., Zerr, Troy, Bowers, Elisabeth, Greene, Elizabeth A., Comai, Luca, Henikoff, Steven

“…Human individuals differ from one another at only ∼0.1% of nucleotide positions, but these single nucleotide differences account for most heritable phenotypic…”
Get full text

Targeted interrogation of copy number variation using SCIMMkit by Zerr, Troy, Cooper, Gregory M., Eichler, Evan E., Nickerson, Deborah A.

“…Copy number variants (CNVs) contribute substantially to human genomic diversity, and development of accurate and efficient methods for CNV genotyping is a…”
Get full text

Systematic assessment of copy-number variant detection via genome-wide single nucleotide polymorphism genotyping by Cooper, Gregory M., Zerr, Troy, Kidd, Jeffrey M., Eichler, Evan E., Nickerson, Deborah A.

“…Single nucleotide polymorphism (SNP) genotyping has emerged as a technology to incorporate copy-number variants (CNVs) into genetic analyses of human traits…”
Get full text

Mapping and sequencing of structural variation from eight human genomes: Making diversity count by KIDD, Jeffrey M, COOPER, Gregory M, HAUGEN, Eric, ZERR, Troy, YAMADA, N. Alice, TSANG, Peter, NEWMAN, Tera L, TÜZÜN, Eray, ZE CHENG, EBLING, Heather M, TUSNEEM, Nadeem, DAVID, Robert, DONAHUE, William F, GILLETT, Will, PHELPS, Karen A, WEAVER, Molly, SARANGA, David, BRAND, Adrianne, WEI TAO, GUSTAFSON, Erik, MCKERNAN, Kevin, LIN CHEN, MALIG, Maika, HAYDEN, Hillary S, SMITH, Joshua D, KORN, Joshua M, MCCARROLL, Steven A, ALTSHULER, David A, PEIFFER, Daniel A, DORSCHNER, Michael, STAMATOYANNOPOULOS, John, SCHWARTZ, David, NICKERSON, Deborah A, MULLIKIN, James C, SAMPAS, Nick, WILSON, Richard K, BRUHN, Laurakay, OLSON, Maynard V, KAUL, Rajinder, SMITH, Douglas R, EICHLER, Evan E, GRAVES, Tina, HANSEN, Nancy, TEAGUE, Brian, ALKAN, Can, ANTONACCI, Francesca

Get full text

Mapping and sequencing of structural variation from eight human genomes by KIDD, Jeffrey M, COOPER, Gregory M, HAUGEN, Eric, ZERR, Troy, YAMADA, N. Alice, TSANG, Peter, NEWMAN, Tera L, TÜZÜN, Eray, ZE CHENG, EBLING, Heather M, TUSNEEM, Nadeem, DAVID, Robert, DONAHUE, William F, GILLETT, Will, PHELPS, Karen A, WEAVER, Molly, SARANGA, David, BRAND, Adrianne, WEI TAO, GUSTAFSON, Erik, MCKERNAN, Kevin, LIN CHEN, MALIG, Maika, HAYDEN, Hillary S, SMITH, Joshu D, KORN, Joshua M, MCCARROLL, Steven A, ALTSHULER, David A, PEIFFER, Daniel A, DORSCHNER, Michael, STAMATOYANNOPOULOS, John, SCHWARTZ, David, NICKERSON, Deborah A, MULLIKIN, James C, SAMPAS, Nick, WILSON, Richard K, BRUHN, Laurakay, OLSON, Maynard V, KAUL, Rajinder, SMITH, Douglas R, EICHLER, Evan E, GRAVE, Tina, HANSEN, Nancy, TEAGUE, Brian, ALKAN, Can, ANTONACCI, Francesca

Get full text