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ABSTRACT: Background
The hybridization of nucleic acid targets with surface-immobilized probes is a widely used assay for the parallel detection of multiple targets in medical and biological research. Despite its widespread application, DNA microarray technology still suffers from several biases and lack of reproducibility, stemming in part from an incomplete understanding of the processes governing surface hybridization. In particular, non-random spatial variations within individual microarray hybridizations are often observed, but the mechanisms underpinning this positional bias remain incompletely explained.Methodology/principal findings
This study identifies and rationalizes a systematic spatial bias in the intensity of surface hybridization, characterized by markedly increased s
SUBMITTER: Steger D
PROVIDER: S-EPMC3157431 | biostudies-literature | 2011
REPOSITORIES: biostudies-literature