Haplotyping the human leukocyte antigen system from single chromosomes von Murphy, Nicholas M., Burton, Matthew, Powell, David R., Rossello, Fernando J., Cooper, Don, Chopra, Abha, Hsieh, Ming Je, Sayer, David C., Gordon, Lavinia, Pertile, Mark D, Tait, Brian D., Irving, Helen R., Pouton, Colin W.

Volltext

LBP36 von Hogan, Hayley M, Dimovski, Karolina, Goodridge, Damian M, Sayer, David C

Volltext

57-OR von Candy, Luke, Hogan, Hayley M, Sayer, David C

Volltext

42-OR von Stone, Emma, Goodridge, Damian M, Sayer, David C

Volltext

104-P von Wirtz, Carla M, Hogan, Hayley M, Alizadeh, Mehdi, Senitzer, David, Gendzekhadze, Ketevan, Iglehart, Brian S, Lind, Curt T, Monos, Dmitrios, Humphreys, Ian, Sayer, David C

Volltext

188-P: A Novel approach to characterizing Exon 3 DRB1 polymrphisms SBT von Hogan, Hayley, Castley, Alison, Goodridge, Damian M, Sayer, David C

Volltext

92-P: Non-Coding Class I Sequences Contain Polymorphisms That Are Specific for Conserved Extended/Ancestral Haplotypes von Sayer, David C, Hogan, Hayley S, Goodridge, Damian M, Castley, Alison, Smith, Linda K

Volltext

282-P: Assign-ATF: Sequence analysis software for HLA and non-HLA applications and Now-Gen and Next-Gen sequencing von Zinetti, Lee-Anne, Goodridge, Damian M, Hodges, Steve, Gilchrist, Tim, Sayer, David C

Volltext

Clinical Applications of Whole-Blood PCR with Real-Time Instrumentation von Castley, Alison, Higgins, Melinda, Ivey, John, Mamotte, Cyril, Sayer, David C, Christiansen, Frank T

Volltext

Intrafamilial transmission of HIV-1 infection from individuals with unrecognized HIV-1 infection von FRENCH, Martyn A, HERRING, Belinda L, KALDOR, John M, SAYER, David C, FURNER, Virginia, DE CHANEET, Christian C, DWYER, Dominic E

Volltext

15-OR: A Multi-Site Study Employing High Resolution HLA Genotyping by Next Generation 454 GS FLX Sequencing von Holcomb, Cherie L, Höglund, Bryan, Anderson, Matthew W, Blake, Lisbeth A, Böhme, Irena, Egholm, Michael, Ferriola, Deborah, Gabriel, Christian, Goodridge, Damian, Klein, Rolf, Ladner, Martha, Lind, Curt, Monos, Dimitri, Pando, Marcelo, Pröll, Johannes, Sayer, David C, Schmitz-Agheguian, Gudrun, Simen, Birgitte B, Thiele, Bernhard, Trachtenberg, Elizabeth, Tyan, Dolly B, Wassmuth, Ralf, White, Shana, Erlich, Henry A

Volltext

OR30 Genetic matching for transplantation using capture probes: Comprehensive and flexible targeted gene sequencing methodology for human leukocyte antigen genes and beyond von Newbound, Christopher N., Hogan, Hayley M., Kolanski, Supaneda N., Dallas, Peter B., Etcell, Jessica A., Goodridge, Damian M., Sayer, David C.

Volltext

LBP36: MATCHING FOR SNP’S IN THE MHC GAMMA BLOCK REDUCES THE RISK OF GVHD AND INCREASES SURVIVAL RATES POST HSCT von Hogan, Hayley M., Dimovski, Karolina, Goodridge, Damian M., Sayer, David C.

Volltext

42-OR: ASSIGN-ATF 1.5: A SEQUENCE ANALYSIS SOFTWARE THAT SIMPLIFIES THE HIGH THROUGHPUT DETECTION OF GENETIC VARIANTS von Stone, Emma, Goodridge, Damian M., Sayer, David C.

Volltext

57-OR: GAMMA-TYPE™: SIMPLE PCR-SSP’S TO ENABLE THE ASSESSMENT OF HAPLOTYPE MATCHING BETWEEN UNRELATED STEM CELL DONORS AND PATIENTS von Candy, Luke, Hogan, Hayley M., Sayer, David C.

Volltext

Population frequencies and putative haplotypes of the killer cell immunoglobulin-like receptor sequences and evidence for recombination von WITT, C. S, DEWING, C, SAYER, D. C, UHRBERG, M, PARHAM, P, CHRISTIANSEN, F. T

Volltext

A quality control program for crossmatching procedures for solid organ transplantation von Howden, Andrea J, Sayer, David C, Bennett, Greg, Smith, Linda K, Christiansen, Frank T

Volltext

104-P: NON-CODING REGIONS OF HLA-B AND -C CONTAIN HAPLOTYPE SPECIFIC POLYMORPHISMS: SHOULD UNRELATED STEM CELL TRANSPLANTS INCLUDE MATCHING OF NON-CODING REGIONS? von Wirtz, Carla M., Hogan, Hayley M., Alizadeh, Mehdi, Senitzer, David, Gendzekhadze, Ketevan, Iglehart, Brian S., Lind, Curt T., Monos, Dmitrios, Humphreys, Ian, Sayer, David C.

Volltext

POPULATION FREQUENCIES AND PUTATIVE HAPLOTYPES OF THE KILLER CELL IMMUNOGLOBULIN-LIKE RECEPTOR SEQUENCES AND EVIDENCE FOR RECOMBINATION1 von Witt, Campbell S., Dewing, Christopher, Sayer, David C., Uhrberg, Marcus, Parham, Peter, Christiansen, Frank T.

Volltext

Assign: a complete software package for allele assignment and quality control of DNA sequencing based typing von Sayer, David C, Goodridge, Damian M

Volltext