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SEQanswers June Challenge Has Begun!

The competition has begun! We're giving away a $50 Amazon gift card to the member who answers the most questions on our site during the month. We want to encourage our community members to share their knowledge and help each other out by answering questions related to sequencing technologies, genomics, and bioinformatics. The competition is open to all members of the site, and the winner will be announced at the beginning of July. Best of luck!

For a list of the official rules, visit (https://www.seqanswers.com/forum/sit...wledge-and-win)
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  • gff2gbSmall

    Hi, everyone.
    I am in trouble converting gff format file to genbank format.

    The gff format file looks like:
    Scaffold_15;HRSCAF=18| StringTie| transcript| 1| 558|1000| .| .| gene_id "STRG.1"; transcript_id "STRG.1.1"; cov "11.043011"; FPKM "0.745167"; TPM "1.132539";
    Scaffold_15;HRSCAF=18| StringTie| exon| 1| 558|1000| .| .| gene_id "STRG.1"; transcript_id "STRG.1.1"; exon_number "1"; cov "11.043011";

    which is generated by StringTie.

    The command is
    gff2gbSmallDNA.pl stringtie.gff gene.fasta stringtie.gb


    However, I got nothing in stringtie.gb.

    Anyone guys who know why I got an empty file.

    Thanks.

  • #2
    Hi jinfang, I face the same issue you are missing max-size-of-gene-flanking-DNA, gff2gbSmall requires 3 parameters plus the output name <gff-file> <seq-file> and <max-size-of-gene-flanking-DNA> <output-name>

    max-size-of-gene-flanking-DNA: specifies how much DNA is included around genes. The value 0 is fine if you want the output to contain only sequences of coding genes.

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