Closed RNAer closed 8 years ago
I'll get started on the HMMER wrapper
awesome!
On Tue, Oct 13, 2015 at 5:43 PM, mortonjt notifications@github.com wrote:
I'll get started on the HMMER wrapper
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@mortonjt , have you got a chance to start working on it? it is probably good to issue pull request of your code as work in progress?
No I haven't gotten around to working on it. Will push probably sometime this weekend.
On Thu, Oct 15, 2015 at 11:04 AM, Zech Xu notifications@github.com wrote:
@mortonjt https://github.com/mortonjt , have you got a chance to start working on it? it is probably good to issue pull request of your code as work in progress?
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needs lots of update. I am doing it.
On Thu, Oct 15, 2015 at 12:01 PM, mortonjt notifications@github.com wrote:
btw, it looks like infernal is already in bfillings https://github.com/biocore/burrito-fillings/blob/master/bfillings/infernal.py
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@RNAer, would it make sense to also include ssu-align? It's based on Infernal but includes SSU specific models, or is there a better method at the moment for annotating SSU?
RNAmmer? but it is a perl script and I am reluctant to use, although it is very highly cited. I plan to just use infernal to do that as it speeds up quite a lot in recent versions. obviously SSU-Align is more accurate, but SSU-Align is designed for aligning many SSU sequences, not for genome annotation. It assumes there's at most 1 SSU in each input sequence, which defeat the purpose.
I thought it would annotate all SSU in a sequence? I'm vaguely remembering this now...
On Tue, Oct 20, 2015 at 11:46 AM, Zech Xu notifications@github.com wrote:
RNAmmer? but it is a perl script and I am reluctant to use, although it is very highly cited. I plan to just use infernal to do that as it speeds up quite a lot in recent versions. obviously SSU-Align is more accurate, but SSU-Align is designed for aligning many SSU sequences, not for genome annotation. It assumes there's at most 1 SSU in each input sequence, which defeat the purpose.
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nope. I got that from Eric.
On Tue, Oct 20, 2015 at 10:48 AM, Daniel McDonald notifications@github.com wrote:
I thought it would annotate all SSU in a sequence? I'm vaguely remembering this now...
On Tue, Oct 20, 2015 at 11:46 AM, Zech Xu notifications@github.com wrote:
RNAmmer? but it is a perl script and I am reluctant to use, although it is very highly cited. I plan to just use infernal to do that as it speeds up quite a lot in recent versions. obviously SSU-Align is more accurate, but SSU-Align is designed for aligning many SSU sequences, not for genome annotation. It assumes there's at most 1 SSU in each input sequence, which defeat the purpose.
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Would it be possible to just use the models from SSU-Align?
On Tue, Oct 20, 2015 at 11:49 AM, Zech Xu notifications@github.com wrote:
nope. I got that from Eric.
On Tue, Oct 20, 2015 at 10:48 AM, Daniel McDonald < notifications@github.com> wrote:
I thought it would annotate all SSU in a sequence? I'm vaguely remembering this now...
On Tue, Oct 20, 2015 at 11:46 AM, Zech Xu notifications@github.com wrote:
RNAmmer? but it is a perl script and I am reluctant to use, although it is very highly cited. I plan to just use infernal to do that as it speeds up quite a lot in recent versions. obviously SSU-Align is more accurate, but SSU-Align is designed for aligning many SSU sequences, not for genome annotation. It assumes there's at most 1 SSU in each input sequence, which defeat the purpose.
— Reply to this email directly or view it on GitHub <https://github.com/biocore/micronota/issues/7#issuecomment-149644865 .
— Reply to this email directly or view it on GitHub https://github.com/biocore/micronota/issues/7#issuecomment-149645411.
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don't think so. I remember the CM model is the same (otherwise, the model in Rfam would be updated with it), but ssualign does something smart in aligning the seq.
oh, lame
On Tue, Oct 20, 2015 at 11:52 AM, Zech Xu notifications@github.com wrote:
don't think so. I remember the CM model is the same (otherwise, the model in Rfam would be updated with it), but ssualign does something smart in aligning the seq.
— Reply to this email directly or view it on GitHub https://github.com/biocore/micronota/issues/7#issuecomment-149646501.
related to issue #6