Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • Muhidini
    Junior Member
    • May 2012
    • 1

    Basic steps in prokaryotic RNAseq data analysis

    Hi all,
    I have tried to browse the SEQanswers forum for my specific question but could not find anything (which does not mean it does not exist...). I am currently working on an RNASeq experiment involving prokaryotic organisms with partly finished/annotated genomes.

    Davis McC (http://seqanswers.com/forums/archive...hp/t-5248.html) has made a very good attempt summarizing the basic steps in RNAseq analysis, but as far as I understood he was describing the analysis for eukaryotes.

    Now my question is whether I can employ the same tools, i.e.:

    1) Get short reads

    2) Map reads against a reference with a short-read aligner like "bwa".

    3) Summarize reads using "Rsamtools" in R. This is where I got stuck, I am not sure how to perform this basic operation- any suggestions ?

    4) Calculate differential gene expression using an R-based package such as "edgeR" or "DSeq" (I have not tried this either, hints ?)

    5) Perform gene-ontology category testing on differentially expressed genes using a package such as "goseq"

    I hope I got these very basic steps right and would be greatful for any hints, tips & tricks, experiences using the abovementioned programs on prokaryotes.

    Thanks for your help and time !
    Cheers
    Lars

Latest Articles

Collapse

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by SEQadmin2, 06-09-2026, 11:58 AM
0 responses
22 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 06-05-2026, 10:09 AM
0 responses
27 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 06-04-2026, 08:59 AM
0 responses
38 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 06-02-2026, 12:03 PM
0 responses
61 views
0 reactions
Last Post SEQadmin2  
Working...