Bioinformatics, Vol 15, 348-355, Copyright © 1999 by Oxford University Press
S Bushnell, J Budde, T Catino, J Cole, A Derti, R Kelso, ML Collins, G Molino, P Sheridan, J Monahan and M Urdea
MOTIVATION: The sensitivity and specificity of branched DNA (bDNA) assays
are derived in part through the judicious design of the capture and label
extender probes. To minimize non-specific hybridization (NSH) events, which
elevate assay background, candidate probes must be computer screened for
complementarity with generic sequences present in the assay. RESULTS: We
present a software application which allows for rapid and flexible design
of bDNA probesets for novel targets. It includes an algorithm for
estimating the magnitude of NSH contribution to background, a mechanism for
removing probes with elevated contributions, a methodology for the
simultaneous design of probesets for multiple targets, and a graphical user
interface which guides the user through the design steps. AVAILABILITY: The
program is available as a commercial package through the Pharmaceutical
Drug Discovery program at Chiron Diagnostics.
ARTICLES
ProbeDesigner: for the design of probesets for branched DNA (bDNA) signal amplification assays
Chiron Diagnostics, 333 Coney Street, Walpole, MA 02032, USA.
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