Departing from these data set, we identified a novel pathway through which thermogenic activation of BAT and the browning of WAT occur via the activation of GPR120 (FFAR4).
Using an in situ 60-mer array platform with more than 20,000 mouse genes derived from the National Institute on Aging clone set, we identified 2,739 genes that were significantly upregulated after differentiation was completed (false-detection ratio <1).
By applying logistic regression analysis to the data set, we identified and weighted the following four independent predictor variables that best discriminate drained lakes from undrained lakes: moraine height-to-width ratio, presence/absence of an ice-core in the moraine, lake area, and main rock type forming the moraine.
From our data set, we identified many reads showing a significant homology with circoviruses.
In the course of defining a novel retinoid-response gene set, we identified a tumor suppressor gene called AKAP12 that was induced with atRA in RASMC [21].
Using this mixed model gene set analysis and by combining weak signals of differential expression across genes within the same gene set, we identified gene sets that were differentially expressed between MS and healthy controls in unstimulated PBMC.
In the same progeny set we identified another isolate (#51) that was disomic for LG 1, which represents one of the largest chromosomes (3.26 Mb) in the genome of M. graminicola isolate IPO323.
Using a custom Perl script and the full data set, we identified 2000 SNPs (minor allele count = 4; minimum coverage = 8; minimum base quality = 20) on chromsome 3R, which are separated by at least 10,500 bp.
31 Across the data set, we identified 171 distinct narratives.
Within our unigene set, we identified a number of genes that would be of comparative interest.
From the AsCIUniGene set we identified four oat CBF genes, denoted AsCBF1, AsCBF2, AsCBF3 and AsCBF4.
