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The gene expression profiles of most human tissues have been studied by determining the transcriptome of whole tissue homogenates.
The utility of the model was tested by determining the transcriptome of the fish upon the exposure to fadrozole, an aromatase inhibitor.
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Using BLAST, we indirectly evaluated the transcriptome coverage breadth by determining the number of unique genes in our collection.
We validated our predictions by determining the significance of our candidate genes in high throughput transcriptome expression profiling studies.
To comprehensively interrogate the molecular features of human prostate epithelial lineages, we determined the transcriptomes of unperturbed benign basal and luminal populations by deep paired-end RNA-Seq.
In this study, we determined the transcriptomes of male and female adult worms of S japonicum by high-throughput RNA-seq with poly-A purified RNA sampoly-A purified
To characterize the microenvironment and niche signaling, we used single cell RNA sequencing (scRNA-Seq) to determine the transcriptomes of 4,391 individual cells.
Recent studies showed that an understanding of the basic mechanisms of adaptation of rickettsiae under various environments, including nutrient deprived medium [11] and temperature changes [38] can be gained by determining their global transcriptome profile by microarrays.
Scatterplots were generated by comparing the log2 fold change determined by the transcriptome analysis and real time PCR.
Cellular identity and function are determined by the transcriptome, i.e. the complete repertoire of expressed RNA transcripts.
Cellular identity and function are determined by the transcriptome or the complete repertoire of expressed RNA transcripts.
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