RSEQtools/workflow

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RSEQtools Main Page

Contents 1 Example workflow 1.1 Prerequisites 1.2 Alignment 1.3 Conversion 1.4 Downstream analyses

Example workflow

This section shows a simple workflow for processing a RNA-Seq data set. A sample data set that was originally published in PNAS is used for this example. Specifically, this sample data set (human embryonic stem cells) consists of 27 nucleotides single-end reads. The reads are aligned to the human reference genome (hg18) and to a splice junction library generated from the UCSC Known Genes annotation set using Bowtie.

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Prerequisites

• Software download:
  • Bowtie

• Download the following data files:
  • chromFa.zip - Human reference genome (hg18), one file per chromosome.
  • hg18.2bit contains the complete hg18 Human Genome in the 2bit format.
  • knownGene.txt.gz - UCSC Known Genes annotation set.
  • knownIsoforms.txt.gz Links together various transcripts (UCSC Known Genes) of a gene into a cluster.
  • sample.fastq.gz - Sample data (hESC; 27nt; single-end; 5 million reads, FASTQ format).

• Decompress the files

 gunzip knownGene.txt.gz knownIsoforms.txt.gz
 unzip chromFa.zip 

• Convert knownGene.txt into the Interval format

 cut -f1,2,3,4,5,8,9,10 knownGene.txt > knownGene.interval

• Generate the composite gene models

 mergeTranscripts knownIsoforms.txt knownGene.interval compositeModel > knownGene_composite.interval

• Create a splice junction library based on the UCSC annotation set

 createSpliceJunctionLibrary hg18.2bit knownGene.interval 20 > knownGene_2x20_spliceJunctions.fa

• Build bowtie index for the reference genome

 bowtie-build -f chr1.fa,chr10.fa,chr11.fa,chr12.fa,chr13.fa,chr14.fa,chr15.fa,chr16.fa,chr17.fa,chr18.fa,chr19.fa,
                 chr20.fa,chr21.fa,chr22.fa,chr2,chr3.fa,chr4.fa,chr5.fa,chr6.fa,chr7.fa,chr8.fa,chr9.fa,chrX.fa,chrY.fa hg18

• Build bowtie index for the splice junction liabrary

 bowtie-build -f knownGene_2x20_spliceJunctions.fa knownGene_2x20_spliceJunctions

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Alignment

• Bowtie alignment of the RNA-Seq reads to the human reference genome

 bowtie -q -p 4 hg18 sample.fastq sample_hg18.bowtie

• Bowtie alignment of the RNA-Seq reads to the splice junction library

 bowtie -q -p 4 knownGene_2x20_spliceJunctions sample.fastq sample_splices.bowtie

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Conversion

• Convert bowtie output to MRF

 bowtie2mrf genomic < sample_hg18.bowtie > sample_hg18.mrf    
 bowtie2mrf junctions < sample_junctions.bowtie > sample_junctions.mrf    

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Downstream analyses

• Calculate gene expression values using the composite gene models

 cat sample_hg18.mrf sample_junctions.mrf | mrfQuantifier knownGene_composite.interval multipleOverlap > sample.geneExpression

• Generate a signal track files in WIG format of the mapped reads

 cat sample_hg18.mrf sample_junctions.mrf | mrf2wig sample

• Generate GFF files representing the splice junctions

 cat sample_hg18.mrf sample_junctions.mrf | mrf2gff sample

• Determine whether there is a mapping bias

 cat sample_hg18.mrf sample_junctions.mrf | mrfMappingBias knownGene_composite.interval > sample.mappingBias 

• Calculate the annotation coverage for the UCSC KnownGene composite gene models

 cat sample_hg18.mrf sample_junctions.mrf | wc -l
 Result: 4760475

 cat sample_hg18.mrf sample_junctions.mrf | mrfAnnotationCoverage knownGene_composite.interval 4760475 500000  1 
 cat sample_hg18.mrf sample_junctions.mrf | mrfAnnotationCoverage knownGene_composite.interval 4760475 1000000 1 
 cat sample_hg18.mrf sample_junctions.mrf | mrfAnnotationCoverage knownGene_composite.interval 4760475 1500000 1 
 cat sample_hg18.mrf sample_junctions.mrf | mrfAnnotationCoverage knownGene_composite.interval 4760475 2000000 1 
 cat sample_hg18.mrf sample_junctions.mrf | mrfAnnotationCoverage knownGene_composite.interval 4760475 2500000 1 
 cat sample_hg18.mrf sample_junctions.mrf | mrfAnnotationCoverage knownGene_composite.interval 4760475 3000000 1 
 cat sample_hg18.mrf sample_junctions.mrf | mrfAnnotationCoverage knownGene_composite.interval 4760475 3500000 1 
 cat sample_hg18.mrf sample_junctions.mrf | mrfAnnotationCoverage knownGene_composite.interval 4760475 4000000 1 
 cat sample_hg18.mrf sample_junctions.mrf | mrfAnnotationCoverage knownGene_composite.interval 4760475 4500000 1