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differential exon usage

Hi everybody!

I've downloaded different bam files (RNA-seq) that corresponds to tumor. I have the coordinates for exons of interest, and I would like to find the differential exon usage over those bam files. I would like to know the best way to do that. Is DEXSeq the best option?

Many thanks in advance!

rna-seq exon bam
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updated by Kristoffer Vitting-Seerup Kristoffer Vitting-Seerup • written by Lila M Lila M

2 answers

If you are looking at differential exon usage (for patient characteristics, tumor-normal, etc.), DEXSeq is a popular option.

I happen to like JunctionSeq (which is based upon DEXSeq), which also includes splice sites (known junctions, and novel junctions between known exons) and an overall p-value for the gene. Sometimes, I could define known differences with JunctionSeq but not DEXSeq.

In both cases, you'll need replicates. If you only had one sample you could try a de novo assembly like cufflinks, but I've found having a merged assembly with multiple samples important for getting robust results (although having split bam files for a high-coverage sample might also be OK).

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written by Charles Warden Charles Warden

Let's say that I have bam files for 3 different treatments and I would like to know the exon usage over a defined exon regions (Let's say exon.bed file). As I downloaded the bam files for a web server, I don't have replicates for each bam file (but apparently, the number of reads is high in each one). As DEXSeq requires as input a count matrix on the exon level, can I create it from my exon.bed file?.Because I don't know exactly how to create it... Otherwise, as I really want to know is the numer of exons included in the bam files, could I run: 

   exon = exon.bed
   featureCounts -a $exon -g gene_name -o overlaps.txt treated_high*.bam  treated_low*.bam untreated*.bam

Many thanks in advance!

Thank you!

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written by Lila M Lila M

DEXSeq uses a specialized scripts (dexseq_prepare_annotation.py and dexseq_count.py) to run HTSeq for exon counts. The manual mentions that you can use other read counting programs, but I would typically use those specifically designed for DEXSeq (using a GTF annotation file).

JunctionSeq uses QoRTs for exon and junction counts.

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written by Charles Warden Charles Warden

I would recommend IsoformSwitchAnalyzeR ( http://bioconductor.org/packages/IsoformSwitchAnalyzeR/ ) which enables statistical identification of isoform switches with predicted functional consequences where the consequences can be chosen from a long list but includes gain/loss of protein domains, signal peptides changes in NMD sensitivity etc.

It requires that you run RSEM or Salmon (probably the better option and much faster) to quantify transcript/isoform expression first - but IsoformSwitchAnalyzeR directly supports both RSEM and Salmon outout.

For other inspiration of other post-analysis of isoform switches take a look at http://mcr.aacrjournals.org/content/early/2017/06/02/1541-7786.MCR-16-0459

Hope this helps

Kristoffer

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written by Kristoffer Vitting-Seerup Kristoffer Vitting-Seerup

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