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Standardisation of Genome Amplification Techniques
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19th SoGAT Meeting
19th SoGAT Meeting
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June 2006 Presentations
Speaker
Title of Talk
Presentation
Session 1: Progress with standardisation
Gerold Zerlauth, Baxter AG, Austria
SoGAT, mission completed or work in progress?
View Presentation
Roberta Madej, Roche, USA
Progress on study to validate synthetic standards
View Presentation
Kurt Roth, GFE Blut mbH, Germany
Competitive vs. Non-competitive Internal Standards
View Presentation
Sally Baylis, NIBSC
Update on the P. falciparum standard and replacement of the HBV and HCV International Standards
View Presentation
Session 2: Hepatitis B
Junko Tanaka, Hiroshi Yoshizawa, Hiroshima University Graduate School of Biomedical Sciences, Japan
Infectious dose and the concentration of HBV DNA in-vitro
View Presentation
Dominique Challine, INSERM, France
Full-length preS1-preS2-HBs antigen (HBsAg) sequence analysis of HBV surface mutants in HBV DNA-positive organ, tissue and cell donors with various HBV serological profiles
View Presentation
Session 3: NAT assay sensitivity/detection limits and new technology
Michael Chudy, Paul-Ehrlich-Institut, Germany
Analytical and diagnostic sensitivity of HCV NAT tests
View Presentation
Markus Sprenger-Haussels, Qiagen, Germany
Generic automated sample preparation for commercial NAT assays
View Presentation
Lutz Pichl, DRK-Blutspendedienst West and Christine Jork, DRK-Blutspendedienst NSTOB, Germany
One year of experience with Roche´s COBAS AmpliPrep/COBAS TaqMan96 automated PCR system in two large blood bank settings
View Presentation
Martin Stolz, Swiss Blood Transfusion Service, Bern, Switzerland
Evaluation of the Procleix Tigris System at the blood transfusion service SRC Berne
View Presentation
Nico Lelie, Chiron, France
Infectivity based risk modelling
View Presentation
Session 4: EQAS schemes
Elizabeth Dax, NRL, Australia
Ongoing quality control programme for testing for blood-borne pathogens through an internet-based application
View Presentation
Thu-Anh Pham, NRL, Australia
An Internet-based application fostering global collaboration of External Quality Assessment Schemes for Nucleic Acid Testing
View Presentation
Vivienne James, HPA, UK
Update on results of recent EQA panels for blood borne viruses
View Presentation
Micha Nübling, Paul-Ehrlich-Institut, Langen, Germany, Karl-Heinz Buchheit, EDQM, Strasbourg, France
Results from recent EDQM/OMCL PTS studies on B19 DNA NAT testing of plasma pools
View Presentation
Matthias Niedrig, Robert Koch Institut, Germany
First international proficiency study on West Nile virus molecular detection
View Presentation
Session 5: Emerging – re-emerging pathogens
Mike Busch, Blood Systems Research Institute USA
Detection of Dengue Viremia in Blood Donations in Brazil and Honduras
View Presentation
Jean-Pierre Allain, University of Cambridge, UK
GB virus C, West Nile virus, and Dengue virus in West Africa
View Presentation
Session 6: NAT for tissues and organs
Simon Carne, NBS, UK
Strategies for Reducing Inhibition of RT-PCR in cadaveric samples
View Presentation
Theo Cuypers, Sanquin Diagnostic Service, The Netherlands
Validation and one year experience with HCV-RNA and HIV-RNA detection in small test pools on cadaveric samples for viral safety of tissue transplants
View Presentation
Susan L. Stramer, ARC, USA
Testing of Haemopoietic Progenitor Cell (HPC) donors
View Presentation
Session 7: Bacterial screening in blood banks
Theo Cuypers, Sanquin Diagnostic Service, The Netherlands
Experience with detection of bacterial contamination of platelet concentrates with NAT, need for biological standards to compare the efficacy of NAT test protocols
View Presentation
Mark Manak, SeraCare Life Sciences, USA
Controls for blood Septicemia Nucleic Acid Tests
View Presentation
Session 8: Parvoviruses
Kevin Brown, HPA, UK
Overview of parvovirus classification (including detection and seroprevalence of Par 4)
View Presentation
Jacqueline Fryer, NIBSC, UK
Novel and related variant parvoviruses in human plasma
View Presentation
Ewa Brojer, Institute of Haematology and Blood Transfusion, Poland
Level of viremia and genotype characteristics of parvo B19 in blood donors and patients
View Presentation
Marco Koppelman, Sanquin Blood Supply Foundation, The Netherlands
Distributions of Parvo virus B19 genotype 1-3 in plasma donations; need for a genotype panel to standardize quantitative Parvo B19 DNA assays for screening
View Presentation
Mei-ying Yu, CBER FDA
Detection of parvovirus B19 variants in Factor VIII concentrates
View Presentation
Peter Simmonds, Ashleigh Manning, Ed Gomperts and the EADS Group
Persistence/reactivation of parvovirus B19 and newly discovered parvoviruses in haemophiliacs exposed to non-virally inactivated factor VIII concentrates HGDS cohort
View Presentation
Nicola Boschetti, ZLB Behring AG, Switzerland
Parvoviruses: A future challenge
View Presentation
Daniel Candotti, University of Cambridge, UK
Maternofetal transmission on human parvovirus B19 genotype 3
View Presentation
Ruth Laub, CAF-DCF Red Cross, Belgium
Is B19-DNA in donation correlated with virus infectivity?
View Presentation
Sean Doyle, National University of Ireland, Maynooth, Ireland
Parvovirus B19 infection in seronegative and seropositive individuals – implications for blood product safety
View Presentation
Sally Baylis, NIBSC, UK
Primer & Probe Design Affects Ability to Detect and Quantify Variant Viruses
View Presentation
Mike Busch, Blood Systems Research Institute USA
Transmissibility of B19 by transfusion: evaluation of donor viremia prior to performing a linked donor-recipient study
View Presentation
Session 9: Genotypes: HIV and other viruses
Indira Hewlett, FDA, Bethesda, USA
HIV variants and a nanoparticle based assay for detection of HIV-1 p24 and RNA
View Presentation
Richard Myers, UCL Medical School, UK
Analysis of Recombination in the HIV-1 pol Gene
View Presentation
Matthias Gessner, Baxter AG, Austria
What about genotypes? (viral genotypes and their relevance in testing)
View Presentation
Concluding session
Gerold Zerlauth, Baxter Hyland Immuno Ag, Austria
SoGAT, mission completed or work in progress revisited
View Presentation
John Saldanha, Roche, USA
Summing up: NAT testing – where are we heading?
View Presentation
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