Hi
I wanted to do differential gene expression testing using RNA-seq data.I have 4 groups. 1 control and 3 diseased.
In each group I have 3 or 4 samples.
G1-4 samples (Control)
G2- 4 Samples (Disease 1)
G3- 3 Samples (Disease 2)
G4- 4 Samples (Disease 3)
In cuffdiff, I have uploaded the combined transcript file from cuffcompare.
Then for the conditions, I have 15 BAM files for 15 samples. In each condition I uploaded each sample (so total no. of conditions would be 15).
I am getting the following error.
Fatal error: Exit code 134 ()
[03:39:08] Loading reference annotation and sequence.
Warning: No conditions are replicated, switching to 'blind' dispersion method
[03:39:31] Inspecting maps and determining fragment length distributions.
[04:02:57] Modeling fragment count overdispersion.
Actually I wanted to download the gene FPKM tracking file from cuffdiff and do the differential gene expression analysis using BRB array tools.
Please help how to solve this.
1 answer
I think you should go like this:
For each condition you generate transcript.gtf
cufflinks -o output_file -G reference_GTF_file bam_file
Then merge all the transcript.gtf of condition for which you want differential gene expression.
cuffmerge -o output_file -g reference_GTF_file transcript.gtf_list
transcript.gtf_list should contain list of all the transcript.gtf to be merged.
then use cuffdiff for differential gene expression.
cuffdiff -o output file merged.gtf bam1 bam2 bam3 .....bamN
bam1, bam2, bam3 are the files of all the condition you want to compare.
Here you will get your gene.fpkm_tracking file.
I hope this would help.
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Hi, was your query solved?