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Transcript Assembly Merge

Obi Griffith edited this page Nov 13, 2016 · 1 revision

RNA-seq Flowchart - Module 5

#4-iii. CUFFMERGE Use Cuffmerge to merge predicted transcripts from all libraries into a unified transcriptome. Refer to the Cufflinks manual for a more detailed explanation:

http://cole-trapnell-lab.github.io/cufflinks/cuffmerge/index.html

Cuffmerge basic usage

cuffmerge [options]* <assembly_GTF_list.txt>

Options specified below:

  • "assembly_GTF_list.txt" is a text file "manifest" with a list (one per line) of GTF files that you would like to merge together into a single GTF file.
  • '-p 8' tells cuffmerge to use eight CPUs
  • '-o' tells cuffmerge to write output to a particular directory
  • '-g' tells cuffmerge where to find reference gene annotations. It will use these annotations to gracefully merge novel isoforms (for de novo runs) and known isoforms and maximize overall assembly quality.
  • '-s' tells cuffmerge where to find the reference genome files

Merge all 4 cufflinks results so that they will have the same set of transcripts for comparison purposes:

For reference guided mode:

cd $RNA_HOME/expression/tophat_cufflinks/ref_guided/
ls -1 *Rep*_ERCC*/transcripts.gtf > assembly_GTF_list.txt
cat assembly_GTF_list.txt
cuffmerge -p 8 -o merged -g $RNA_HOME/refs/hg19/genes/genes_chr22_ERCC92.gtf -s $RNA_HOME/refs/hg19/bwt/chr22_ERCC92/ assembly_GTF_list.txt

For de novo mode:

cd $RNA_HOME/expression/tophat_cufflinks/de_novo/
ls -1 *Rep*_ERCC*/transcripts.gtf > assembly_GTF_list.txt
cat assembly_GTF_list.txt
cuffmerge -p 8 -o merged -g $RNA_HOME/refs/hg19/genes/genes_chr22_ERCC92.gtf -s $RNA_HOME/refs/hg19/bwt/chr22_ERCC92/ assembly_GTF_list.txt

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