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bedcoverage output while looking for missing genes

Hi,

I´m trying to identify missing genes in my bacterial assembly compared to my reference genome. I have run coverageBed as follows:

coverageBed  -a  Staph.genomic.gff -b  Staph_assembly.sorted.bam

I´m not sure i understand all columns so i was wondering if you could help me on identifyong the column with missing gene information and what are the columns correspond to. Thanks !!!

ACVP01000037.1  Genbank gene    1312    2169    .       +       .       ID=gene1;Name=CORTU0001_0103;gbkey=Gene;gene_biotype=protein_coding;locus_tag=CORTU0001_0103    0       0       858     0.0000000
ACVP01000037.1  Genbank CDS     1312    2169    .       +       0       ID=cds1;Parent=gene1;Dbxref=NCBI_GP:EET76330.1;Name=EET76330.1;gbkey=CDS;product=hypothetical protein;protein_id=EET76330.1;transl_table=11     0       0       858     0.0000000
ACVP01000037.1  Genbank gene    2228    2350    .       -       .       ID=gene2;Name=CORTU0001_0104;gbkey=Gene;gene_biotype=protein_coding;locus_tag=CORTU0001_0104    0       0       123     0.0000000
ACVP01000037.1  Genbank CDS     2228    2350    .       -       0       ID=cds2;Parent=gene2;Dbxref=NCBI_GP:EET76331.1;Name=EET76331.1;Note=identified by glimmer%3B putative;gbkey=CDS;product=hypothetical protein;protein_id=EET76331.1;transl_table=11      0       0       123     0.0000000
ACVP01000037.1  Genbank gene    2321    3673    .       +       .       ID=gene3;Name=CORTU0001_0106;gbkey=Gene;gene_biotype=protein_coding;locus_tag=CORTU0001_0106    0       0       1353    0.0000000
bedtools
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updated by Kevin Blighe Kevin Blighe • written by David David

1 answer

The BEDTools documentation (here) states the following:

After each interval in A, bedtools coverage will report:

  • The number of features in B that overlapped (by at least one base pair) the A interval.
  • The number of bases in A that had non-zero coverage from features in B.
  • The length of the entry in A.
  • The fraction of bases in A that had non-zero coverage from features in B.

So, you have to look to the right-most part of your output, specifically the final 4 columns. In the small amount of data that you have pasted, I can therefore see that no BAM reads overlapped these exons that were in your input GFF.

Note that you may also be interested in the -hist parameter. Take a look at the dicumentation for this and more information.

Kevin

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written by Kevin Blighe Kevin Blighe

Thanks Kevin, I went trough the bedtools but didn´t find clearly that it was the last 4 columns. Thanks for letting me know.

• 1 views • link
written by David David

No problem David - best of luck.

• 1 views • link
written by Kevin Blighe Kevin Blighe

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