Popular brain transcriptome methods are powerful at detecting global gene expression. These approaches, however, fail to capture gene expression from small cellular groups in a heterogeneous organ such as the developing brain. We developed a high resolution transcriptome (HRT) method to determine the full repertoire of transcripts in neural stem cells, migrating neurons, and differentiating neurons. Using HRT, we defined five transcriptional programs that govern different developmental mechanisms such as stem cell maintenance, neurogenesis, migration, and differentiation. These five transcriptional programs contain largely uncharacterized genes as well as intergenic transcriptionally active regions that possibly encode novel transcripts.
You can perform a quick search for your gene of interest in the box below. Expression levels and layer distribution will be presented in a histogram. Additional information can be found in Ayoub et al 2011 and in Supporting Information. Raw sequence and mapped data for this study has been deposited in the Gene Expression Omnibus (GSE30765).
RPKM values and statistics for differentially expressed genes: Genes.xls
RPKM values and statistics for differentially expressed transcripts:Transcripts.xls
RPKM values and statistics for differentially expressed exons: Exons.xls
RPKM values and statistics for differentially expressed novel TARs: nTARs.xls
Genomic location for all enhancers near differentially expressed genes: Enhancers.xls