Sentence examples for microarray hybridization technique from inspiring English sources

The oligonucleotide microarray hybridization technique identified reliably and correctly all samples.

In addition, the choice of SAGE versus microarray hybridization technique depends on several factors, such as the scope of the genetic screen, the number of samples, the amount of starting material and the availability of resources such as an automated DNA sequencer.

This technique has evolved from pioneering studies utilizing microarray hybridization techniques to score presence/absence of marker regions adjacent to restriction sites in the genome [23], to exploit next-generation techniques to directly sequence these regions [6].

The reliability of microarray hybridization techniques were confirmed by the company-supplied hybrydization control.

The phases of the rhythms of both clock genes, as well as the melatonin biosynthesis genes, were similar when measured using either qPCR or microarray hybridization techniques.

A variety of methods has been developed to conduct genome-scale analyses of DNA methylation, ranging from microarray hybridization techniques to DNA methylation profiling by whole-genome shotgun bisulfite sequencing (WGSBS), the latter yielding genome-wide methylation data in single-base resolution (Bock et al. 2010).

In contrast, Diversity Arrays Technology (DArT) is a microarray hybridization based technique that permits simultaneous screening thousands of polymorphic loci without any prior sequence information [ 34].

Diversity arrays technology (DArT), a microarray hybridization-based technique, has been developed in common wheat for high-throughput genotyping without relying on sequence information.

Analysis of these libraries by cDNA microarray hybridization and other techniques identified distinct patterns of expression of transcripts of polysaccharide-related enzymes in stem peels during fibre elongation and cell wall deposition.

This may explain why EHHADH, HMGCR and HMGCS2 were observed as differentially expressed by qRT-PCR but not by microarray; and it may suggest that the microarray analyses based on hybridization technique is more hampered by proportion of false negative compared to qRT-PCR analyses because of the lack of an amplification step.

DGE is very similar in the sampling approach to long oligonucleotide probe microarray hybridization, given that both techniques take short nucleic acid target sequences to sample expression of longer RNA molecules containing them, and both are 3' biased because they rely on extension of cDNAs from the polyA tail with a oligo-dT primer.