This work was supported in part by the National Heart, Lung, and Blood Institute Contracts N01-HB-97077 (superseded by N01-HB-47114), -97078, -97079, -97080, -97081, and -97082 through the Retrovirus Epidemiology Donor Study. Data on plasma donor panels were provided by Alpha Therapeutic Corporation and National Genetics Institute (NGI) and testing reagents by the manufacturers of the NAT assay systems (Roche Molecular Systems and Gen-Probe Inc.).
Relative sensitivities of licensed nucleic acid amplification tests for detection of viremia in early human immunodeficiency virus and hepatitis C virus infection†
Version of Record online: 18 OCT 2005
Volume 45, Issue 12, pages 1853–1863, December 2005
How to Cite
Busch, M. P., Glynn, S. A., Wright, D. J., Hirschkorn, D., Laycock, M. E., McAuley, J., Tu, Y., Giachetti, C., Gallarda, J., Heitman, J., Kleinman, S. H. and National Heart, Lung, Blood Institute Nucleic Acid Test Study Group (2005), Relative sensitivities of licensed nucleic acid amplification tests for detection of viremia in early human immunodeficiency virus and hepatitis C virus infection. Transfusion, 45: 1853–1863. doi: 10.1111/j.1537-2995.2005.00649.x
- Issue online: 18 OCT 2005
- Version of Record online: 18 OCT 2005
- Received for publication March 20, 2005; revision received May 5, 2005, and accepted May 9, 2005.
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