RNA-Seq uses next-gen sequencing to show the presence and quantity of RNA in a genome at a particular moment. DNASTAR’s SeqMan NGen application is the starting point for both reference-guided and de novo RNA-Seq workflows. Because this tutorial involves a reference-guided workflow, you will then use ArrayStar to analyze the completed RNA-Seq assembly.
In this tutorial, you will compare stationary phase RNA from wild-type E. coli cells with that from two different mutant cells, each lacking one of two genes that together encode a transcription factor for flagella and chemotaxis operons. The data is publically-available single-end Illumina data from E. coli (Fitzgerald et al, 2014). During downstream analysis, you will be able to visually identify these operons in ArrayStar’s Gene Table.
IMPORTANT! There are two options for following this tutorial, one significantly longer than the other.
|Item||Full tutorial||Abbreviated tutorial|
|Description||Assemble in SeqMan NGen, then do downstream analysis in ArrayStar||Do only the downstream analysis in ArrayStar, using a provided project|
|Download size||3.9 GB||4 MB|
|Assembly wait time||1-3 hours||none|
|Where to begin||Perform the steps in Part A: Setting up an RNA-Seq reference-guided assembly in SeqMan NGen||Read the steps in Part A: Setting up an RNA-Seq reference-guided assembly in SeqMan NGen without performing them|
Need more help with this?