Thanks Antonio..
That's a great help.. one last question.. I am interested in Alternative Splicing and novel isoforms (if any).. Any further suggestion?..
Cheers
Fahim
Hi there,
I am about to run cufflinks on my TOPHAT bam files for Arabidopsis. I guess I will have to use mapped.bam files for my samples.
What reference genome should I use for cufflinks?
ENSEMBL19
or
TAIR10
I want to make sure that I get gene names instead of XLOC id in cummeRbund..
Your advice is very precious for me. Thank you.
There is a paper around "A comprehensive evaluation of ensembl, RefSeq and UCSC annotations in the context of RNA-seq read mapping and gene quantification. Zhao and Zhang BMC Genomics (2015) 16:97 that evaluates the effect of different annotations in your data
This affects to only a small set of genes, those that are annotated in a different way in different assemblies
If this is something concerning you, use both reference genomes, and compare
Thanks Antonio..
That's a great help.. one last question.. I am interested in Alternative Splicing and novel isoforms (if any).. Any further suggestion?..
Cheers
Fahim
If using RNA-Seq, I would suggest you to use the latest version of limma under R
The vignette this program provides is very clear and intuitive
Thanks Antonio..
I will try Limma.. I hope there is GUI.. I have little understanding of commands and programming..
Have a great day.
Fahim
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