What is the best (options) for analyzing a Illumina Seq data for ncRNA including lincRNA. Is there a standard work flow?
Thanks
What is the best (options) for analyzing a Illumina Seq data for ncRNA including lincRNA. Is there a standard work flow?
Thanks
If you are looking for novel lncRNA, then here is nice pipeline , they use RABT assembly, and the cufcompare, and then they run lncRscan script on the outputs.
http://www.biomedcentral.com/1471-2105/13/331/figure/F1
from the study
http://www.biomedcentral.com/1471-2105/13/331
If not, then just map your reads, TopHat or STAR, then run cufflinks providing lncRNA or ncRNA GTF file (http://www.gencodegenes.org/releases/19.html)
then do some filtering, FPKM thresholds, or length thresholds.
HTH
There are some methods paper.
However you could always start like
Hi,
I wrote a similar pipeline which also categorizes lncRNAs into different classes. Take a look: http://git.io/SaFh1g
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Depends on the organism. For human/mouse/etc. there are some OK annotations via lncRNAdb, Ensembl, etc. that you could start with.
It is human I can use Broad database. I am more concerned about how I can reach at a final list of differential list of ncRNA.
do you mean differential expression, or just the list which is detected in one but not in other ?
Yes present in one samples.but not in other
In this case , run the pipeline shown
http://www.biomedcentral.com/1471-2105/13/331/figure/F1
then see which transcript you find in one sample but not in others