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Differential Expression based on Sequences from lncRNA

Hi, first of all, thank you for existing ! I am somewhat new to bioinformatics but I've learned much in the last year. I am familiar with running RNAseq pipelines in order to get differentially expressed genes using DEseq, HTSeq, cufflink, EdgeR etc...BUT, I am facing something new; I have total RNAseq data and would like to see if some long non-coding RNAs are differentially expressed in my patients. I have their positions and their sequences. But they are not "identified" in databases so they're not part of the gene reference file.

My question is: is it possible at all to get differential expression based off of sequences?

Would I have to manually change my gene.gtf ?.. Any help would be welcome.

Thank you very much

J.

rna-seq sequence
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updated by Ram Ram • written by Joel TM Joel TM

You can create a bed file with lncRNA coordinates and count how many reads mapped to each lncRNA using bedtools multicov and perform DESeq/edgeR analysis.

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updated by Ram Ram • written by GouthamAtla GouthamAtla

Ok thank you, I'll be trying that asap.

[EDIT] Works like a charm. Thank you very much

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written by Joel TM Joel TM

1 answer

You can create a bed file with lncRNA coordinates and count how many reads mapped to each lncRNA usingbedtools multicov and perform DESeq/edgeR analysis.

A small note: You should keep in mind that bedtools do not take care of paired-end data i.e it will count reads per region instead of fragments per region.

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updated by Ram Ram • written by GouthamAtla GouthamAtla

Thanks for the detail! I read something about that too. I was too impatient so I tried it with the Tophat output (a single .bam file). The data we have is indeed paired ends though. I understand the results could be different from reality, but I don't know to what extent. Would utilizing only the forward strand be better ?

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written by Joel TM Joel TM

There would not be much difference. Its just that you need to keep in mind. Still you can create a dummy gtf file with your coordinates and use htseq-count. Something like:

chr1    source    lncRNA    100    200    lncRNA_id="chr1:100-200"
chr1    source    lncRNA    500    600    lncRNA_id="chr1:500-600"

Now try htseq-count with -i lncRNA_id.

If you know what exactly htseq is doing, you can create a dummy gff/gtf and use htseq-count to get fragment level counts.

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updated by Ram Ram • written by GouthamAtla GouthamAtla

That is good info, thank you for all your help ! :)

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written by Joel TM Joel TM

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