Open agroppi opened 5 years ago
When I look into my Marouch_transcripts.fasta
file I have :
>jg25328.t1 jg25328
>jg25224.t1 jg25224
>jg25204.t1 jg25204
>jg25354.t1 jg25354
>jg25354.t2 jg25354
>jg25351.t1 jg25351
...
>jg64.t1 jg64
>jg53.t3 jg53
>jg53.t1 jg53
>jg53.t2 jg53
...
Would "t1, "t2", "t3"... be the equivalent of "seq1", "seq2", "seq3" in a Trinity.fasta ?
Therefore, in this case, the gene-to-transcript mapping file would it be something like this ? :
jg25328 jg25328.t1
jg25224 jg25224.t1
jg25204 jg25204.t1
jg25354 jg25354.t1
jg25354 jg25354.t2
jg25351 jg25351.t1
...
jg64 jg64.t1
jg53 jg53.t3
jg53 jg53.t1
jg53 jg53.t2
...
Thanks
Right, make the gene-to-transcript file like your suggested version, but just be sure to include tabs as separators.
best,
~brian
On Tue, Sep 18, 2018 at 5:56 AM Alexis Groppi notifications@github.com wrote:
When I look into my Marouch_transcripts.fasta file I have :
jg25328.t1 jg25328 jg25224.t1 jg25224 jg25204.t1 jg25204 jg25354.t1 jg25354 jg25354.t2 jg25354 jg25351.t1 jg25351 ... jg64.t1 jg64 jg53.t3 jg53 jg53.t1 jg53 jg53.t2 jg53 ...
Would "t1, "t2", "t3"... be the equivalent of "seq1", "seq2", "seq3" in a Trinity.fasta ?
Therefore, in this case, the gene-to-transcript mapping file would it be something like this ? :
jg25328 jg25328_t1 jg25224 jg25224_t1 jg25204 jg25204_t1 jg25354 jg25354_t1 jg25354 jg25354_t2 jg25351 jg25351_t1 ... jg64 jg64_t1 jg53 jg53_t3 jg53 jg53_t1 jg53 jg53_t2 ...
Thanks
— You are receiving this because you are subscribed to this thread. Reply to this email directly, view it on GitHub https://github.com/Trinotate/Trinotate.github.io/issues/7#issuecomment-422331508, or mute the thread https://github.com/notifications/unsubscribe-auth/AHMVX_yGoz1WZ3sYqZvDd5dnB4b30eNfks5ucMM7gaJpZM4WsH0K .
Brian J. Haas The Broad Institute http://broadinstitute.org/~bhaas http://broad.mit.edu/~bhaas
Hi,
I'm trying to use trinotate using data from gene prediction produced by Braker2.0 (augustus). Thank to your help I managed to go through the first step of Transdecoder (https://github.com/TransDecoder/TransDecoder/issues/72 ) I have run all the step described here : https://github.com/Trinotate/Trinotate.github.io/wiki/Software-installation-and-data-required#3-running-sequence-analyses But I have some doubt about the first step of "Loading generated results into a Trinotate SQLite Database" My concern is about producing a gene-to-transcript mapping file. From which file can it be constructed ?
Here are below all the data I have now in my Trinotate working directory :
Thanks