We designed an ssDNA-GNP probe to target and visually detect the CpG region of the tumor suppressor genes by introducing a colorimetric method to modify an existing bisulfite-based method that measures CpG region methylation.
QUASI is a codon-based method that measures empirical dN/dS ratios at each codon and compares these statistically to neutral dN/dS ratio using two-binomial distribution.
We measured induction of Nrf2 activity in whole lung nuclear protein extracts from WT, p47phox−/− and gp91phox−/ mice using an ELISA-based method that measures binding of Nrf2 to its oligonucleotide target.
We used a newly developed Universal single telomere length assay (STELA) [ 8], a PCR-based method that measures the telomere length on single human chromosome arms.
Here, we used an entropy-based method that measures the pure three-way epistatic interaction after subtracting out the one-way and two-way genetic effects [Hu et al., 2011; Hu et al., 2013a, b].
This is an MTT-based method that measures the ability of the mitochondria of metabolically active cells to convert tetrazolium salt into a blue formazan product, which is then measured colorometrically at 595 nm; Cell Proliferation Reagent (WST-1; Roche).
The DEA analysis is a mathematical programming based method that converts multiple input and output measures into a single summary measure of production efficiency.
Further overview of the DEA model is presented below For assessing differences in the productive efficiency of health centres, we use DEA, a mathematical programming based method that converts multiple input and output measures into a single summary measure of productive efficiency.
MHCIIMulti [ 12] is a kernel based method that makes use of multi-instance technique for measuring the similarity between peptides.
In addition, the hybridization based methods that are generally used to measure the abundance of individual mutants by STM or TRASH, require relative large amounts of DNA or RNA and exhibit a limited dynamic range.
