Use Lasergene Genomics to get the whole picture of your RNA-Seq data.
RNA-seq is currently one of the leading technologies available for exploring the transcriptome, which is crucial to connecting the information about a genome with its functional protein expression. But RNA-Seq data analysis can prove to be a challenge for many researchers as the applications for this technology are quite broad. Lasergene Genomics quickly and easily aligns any size RNA-Seq or miRNA data set — from bacteria to human— against a reference genome, and then offers extensive analysis of the aligned data so that you can explore in-depth. Perform statistical analyses of differential gene expression using EdgeR or DESeq2, easily identify genes of interest using comprehensive filtering tools, utilize gene ontologies to identify the relationship between genes with known biological functions, easily visualize and analyze mRNA isoforms using Sashimi plots, see variants detected in the sequencing data, and more. We don’t always know what we are looking for when we begin RNA-Seq analysis. Lasergene Genomics makes it easy to explore points of interest so that you can get the whole picture of your data set.
