
ABSTRACT To optimize oligonucleotide probe design criteria, PCR products with different similarities to probes were hybridized to a functional gene microarray designed to detect homologous genes from different organisms. In contrast to more restrictive probe designs based on a single criterion, simultaneous consideration of the percent similarity (≤90%), the length of identical sequence stretches (≤20 bases), and the binding free energy (≥−35 kcal mol −1 ) was found to be predictive of probe specificity.
info:eu-repo/classification/ddc/570, Oligonucleotide Probes: genetics, Base Sequence, Oligonucleotide Probes: chemistry, Nucleic Acid Hybridization, Polymerase Chain Reaction, J, Drug Design, Environmental Microbiology, Thermodynamics, Oligonucleotide Probes, Oligonucleotide Array Sequence Analysis: statistics & numerical data, Oligonucleotide Array Sequence Analysis: methods, Oligonucleotide Array Sequence Analysis
info:eu-repo/classification/ddc/570, Oligonucleotide Probes: genetics, Base Sequence, Oligonucleotide Probes: chemistry, Nucleic Acid Hybridization, Polymerase Chain Reaction, J, Drug Design, Environmental Microbiology, Thermodynamics, Oligonucleotide Probes, Oligonucleotide Array Sequence Analysis: statistics & numerical data, Oligonucleotide Array Sequence Analysis: methods, Oligonucleotide Array Sequence Analysis
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