Miller, C.J., Kassem H.S., Pepper S.D., Hey Y., Ward T.H., Margison G.P. «Mycoplasma infection significantly alters
microarray gene expression profiles.»
Not exact matches
One of these, his most influential, outlines his original use of
microarray expression profiles as a phenotypic footprint for
gene function.
Using quantitative RT - PCR we confirmed the
expression profile of five
genes (colony - stimulating factor 1 receptor [Csf1r], Cd68, Pex11a, Emr1, and Mcp1) in each of the 24 samples and found excellent agreement between the
microarray and RT - PCR
expression data (mean Pearson correlation coefficient = 0.91,
microarray versus RT - PCR
expression; Supplemental Table 3, http://www.jci.org/cgi/content/full/112/12/1796/DC1).
To detect novel changes in
gene expression, we used a focused
microarray platform to evaluate the
expression profile of retinas from hypoxic animals compared to that in retinas isolated from control animals exposed to room air.
We offer a wide range of services, including capillary sequencing and genotyping, Illumina
microarray - based
gene expression profiling and genotyping, and next - generation sequencing (NGS).
This is an advantage of RNA - seq and
microarray - based
expression profiling, which can't always distinguish between multiple promoters of the same
gene.
This will be achieved by exposing the coral to seawater with high calcium concentrations to induce an alteration in
gene expression profiles, identified using a DNA
microarray analysis.
Calcification rate measurements and
gene expression analysis by
microarray RNA transcriptional
profiling at two time - points (midday and night - time) revealed several
genes common within mammalian
gene regulatory networks.
Unfortunately, direct comparisons of
gene expression profiles obtained in independent, publicly available
microarray experiments are typically compromised by substantial, experiment - specific biases.
The Gladstone team had
profiled changes in
gene expression using DNA
microarrays, which provides an unbiased method for identifying key biological pathways.
Proteomic analysis to
profile protein abundance resulted in the identification and relative quantification for 912 proteins with two or more unique peptides and 86 proteins with significant abundance changes after treatment with the neurotoxins, while
microarray analyses to
profile gene expression revealed 181
genes with significant changes in mRNA after treatment.
Another widely used technology to
profile gene expression levels is
microarrays.
The aim of his research was to use
microarray gene expression data in order to characterize ageing in different human tissues and identify the age at which major changes in genetic
expression profiles occur.
Quantitative real time PCR (qRT - PCR) is accepted as the gold standard for
expression profiling, so we next compared both our RNAseq and the
microarray expression estimates to a panel of qRT - PCR TaqMan
gene expression assays (Figure 2C — F).
Comparison of
gene expression profiles obtained by Q - PCR (left panels) and
microarray analysis (right panels).
Specifically, we have generated clusters of transcripts that behave the same way under the entire spectrum of the sixty - seven experimental conditions; we have assembled
genes in groups according to their time of
expression during successive days of ES cell differentiation; we have included expression profiles of specific gene classes such as transcription regulatory factors and Expressed Sequence Tags; transcripts have been arranged in «Expression Waves» and juxtaposed to genes with opposite or complementary expression patterns; we have designed search engines to display the expression profile of any transcript during ES cell differentiation; gene expression data have been organized in animated graphs of KEGG signaling and metabolic pathways; and finally, we have incorporated advanced functional annotations for individual genes or gene clusters of interest and links to microarray and genomic
expression during successive days of ES cell differentiation; we have included
expression profiles of specific gene classes such as transcription regulatory factors and Expressed Sequence Tags; transcripts have been arranged in «Expression Waves» and juxtaposed to genes with opposite or complementary expression patterns; we have designed search engines to display the expression profile of any transcript during ES cell differentiation; gene expression data have been organized in animated graphs of KEGG signaling and metabolic pathways; and finally, we have incorporated advanced functional annotations for individual genes or gene clusters of interest and links to microarray and genomic
expression profiles of specific
gene classes such as transcription regulatory factors and Expressed Sequence Tags; transcripts have been arranged in «
Expression Waves» and juxtaposed to genes with opposite or complementary expression patterns; we have designed search engines to display the expression profile of any transcript during ES cell differentiation; gene expression data have been organized in animated graphs of KEGG signaling and metabolic pathways; and finally, we have incorporated advanced functional annotations for individual genes or gene clusters of interest and links to microarray and genomic
Expression Waves» and juxtaposed to
genes with opposite or complementary
expression patterns; we have designed search engines to display the expression profile of any transcript during ES cell differentiation; gene expression data have been organized in animated graphs of KEGG signaling and metabolic pathways; and finally, we have incorporated advanced functional annotations for individual genes or gene clusters of interest and links to microarray and genomic
expression patterns; we have designed search engines to display the
expression profile of any transcript during ES cell differentiation; gene expression data have been organized in animated graphs of KEGG signaling and metabolic pathways; and finally, we have incorporated advanced functional annotations for individual genes or gene clusters of interest and links to microarray and genomic
expression profile of any transcript during ES cell differentiation;
gene expression data have been organized in animated graphs of KEGG signaling and metabolic pathways; and finally, we have incorporated advanced functional annotations for individual genes or gene clusters of interest and links to microarray and genomic
expression data have been organized in animated graphs of KEGG signaling and metabolic pathways; and finally, we have incorporated advanced functional annotations for individual
genes or
gene clusters of interest and links to
microarray and genomic resources.
The results show comparable
gene expression profiles between
microarray and Q - PCR data.