Base pair interactions and hybridization isotherms of matched and mismatched oligonucleotide probes on microarrays
Hans Binder, Stephan Preibisch, Toralf Kirsten
Abstract
The lack of specificity in microarray experiments due to non-specific hybridization raises a serious problem for the analysis of microarray data because the residual chemical background intensity is not related to the expression degree of the gene of interest. We analyzed the concentration dependence of the signal intensity of perfect match (PM) and mismatch (MM) probes in terms using a microscopic binding model using a combination of mean hybridization isotherms and single base related affinity terms. The signal intensities of the PM and MM probes and their difference are assessed with regard to their sensitivity, specificity and resolution for gene expression measures. The presented theory implies the refinement of existing algorithms of probe level analysis to correct microarray data for non-specific background intensities.
Create a lesson
Related papers
Discrete Backbone Elasticity and Curvature-Dependent Torsion Statistics in Proteins
Yiquan Wang, Mingyu Bian, Jiayuan Ma
Ablating Design Choices for Protein Ensemble Generators Across Structural Regimes
Eoin Quinn, Oliver Bent
Predicting protein structures at any folding stage from sequence
Lisheng Zhang, Qingsong Li, Zinan Xie et al.
Automatic Generation of Novel Highly-Functional Molecular Sequences
Vincent R. Ragusa, Chrisoph Adami
D2ML: Models for Direct-to-Biology Small Molecule Screening
AkshatKumar Nigam, Neri Amara, Hillary Dequina et al.
Contribution of chromosome-naïve transposon-seeded network of DNA templates to intracellular pools of protein dimers of liquid-liquid phase-separated condensate-forming proteins
Gennadi Glinsky