Sentence examples for microarray results i from inspiring English sources

Two different analysis paradigms were used for the evaluation of the microarray results: (i) overall evaluation using SAM analysis and (ii) evaluation targeting the specific biological pathways of interest, lipid metabolism and inflammation.

Nine differentially expressed genes were selected based on the microarray results (i.e., 2-12 fold changes) and putative gene functions were selected and analyzed using real-time quantitative RT-PCR.

For all of the genes selected, the qRT-PCR results were always in the same direction as the microarray results (i.e. increased transcript levels for a given gene found using microarrays was also found to be increased by qRT-PCR) but the dynamic range for the transcript changes was greater in the qRT-PCR assays.

Microarray results indicated that collagen type I alpha 2 was the most abundant transcript and was not differentially expressed between unfused and fused suture tissues (1.05 fold, Table 3).

To verify the microarray results in a direct fashion (i.e. without intervening reverse-transcription and amplification steps), we then performed double-blind in-situ hybridization for four candidate genes in human motor cortex sections from five control and five SALS subjects.

As expected from microarray results, no change in MHC class I molecule expression was detected at the surface of LPS stimulated PBMCs for 24 hours.

To identify SRF-dependent genes, I filtered the microarray results to isolate the set of transcripts whose expressions were reduced by more than 1.5 fold with SRF-specific siRNA after 1 h of zymosan treatment.

These two independent measures, by microarray and qRT-PCR, of transcript abundance gave consistent results, i.e. similar fold changes were observed (see Additional file 1: Figure S1).

To validate the microarray results, one microgram of total RNA was incubated with DNase I, and reverse transcribed with oligo dT using Superscript II RT-PCR (Invitrogen).

To validate the protein microarray results, we selected 11 TFs with different mCpG-dependent DNA-binding behaviors (i.e., sequence-dependent or -independent).

Our microarray results indicate no significant decrease in their mRNA levels in any BaP treatment group (Supporting Information Table I; Table I).