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  • Difficulty using .gtf file in featureCounts read summarization

    Hello,

    I am doing differential expression analysis on an insect bacterial endosymbiont. I have Illumina HiSeq reads that are paired-end and strand-specific.

    I have mapped my reads to a preliminary genome assembly for the endosymbiont with bbmap, and am trying to summarize the results with featureCounts. I annotated the preliminary genome with RAST, and am having difficulty using the exported .gtf file from RAST in featureCounts.

    This is a sample annotation from RAST:

    tig00000001_pilon FIG CDS 734 1288 . + 2 ID=fig|707884.3.peg.1;Name=Mobile element protein

    I am interested in summarizing at the MetaFeature level, since there is really no difference between genes and exons in this case. I used the below command (knowing that the Name field probably wasn't what featureCounts was looking for, since it doesn't represent a unique identifier).

    featureCounts(files=c("file1.bam","file2.bam","file3.bam","file4.bam","file5.bam","file6.bam","file7.bam","file8.bam"),strandSpecific=2,isPairedEnd=TRUE,requireBothEndsMapped=TRUE,isGTFAnnotationFile=TRUE,GTF.attrType="ID",GTF.featureType="Name",useMetaFeatures=TRUE,annot.ext="/path/to/file/file.gtf")

    I got this error:

    || WARNING no features were loaded in format GTF. ||
    || annotation format can be specified using '-F'. ||
    Failed to open the annotation file /path/to/file/file.gtf, or its format is incorrect, or it contains no 'exon' features.
    Error in file(file, "rt") : cannot open the connection
    In addition: Warning message:
    In file(file, "rt") :
    cannot open file './.Rsubread_featureCounts_pid40183': No such file or directory



    I then tried to edit the .gtf file to comply a bit better with the format specifications that I saw described (giving a unique identifier to 'exon', etc.):

    tig00000001_pilon FIG CDS 734 1288 . + 2 gene_id 707884.3.peg.1; exon 707884.3.peg.1.1

    I ran the below command, but I got the exact same error:

    featureCounts(files=c("file1.bam","file2.bam","file3.bam","file4.bam","file5.bam","file6.bam","file7.bam","file8.bam"),strandSpecific=2,isPairedEnd=TRUE,requireBothEndsMapped=TRUE,isGTFAnnotationFile=TRUE,GTF.attrType="gene_id",GTF.featureType="exon",useMetaFeatures=TRUE,annot.ext="/path/to/file/file.gtf")

    Is there something fundamentally wrong that I'm doing here?

    Thanks!
    Ryan

  • #2
    At a minimum chromosome identifiers have to perfectly match between your bam files and the GTF files. Check that first.

    Comment


    • #3
      Hi GenoMax.

      Yes, the chromosome/contig names are identical between the bam and gtf files. Does featureCounts strictly require another line for each entry that corresponds to a feature, like "exon"?

      Comment


      • #4
        I don't think so. Your GTF file is likely not in the correct format. Check that as well.

        Comment

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