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License: GNU General Public License v3.0
CPT's Galaxy Tools
License: GNU General Public License v3.0
This tool is on the EU Galaxy and is really nice for aggregating multiple fastQC files. It can do a lot more than that, but currently, the only way to aggregate such reports is to concatenate files, which creates redundant and useless data, so this tool should help with that on my assembly workflow and for future data analysis. This is the website of the tool, here is the github site and the toolshed link is here.
CRISPR-finder for finding repeats: http://crispr.i2bc.paris-saclay.fr/Server/
PHASTER for finding the proteins: http://phaster.ca/
When browsing hits in the InterPro Scan evidence track, can we add a direct link to the Interpro website with that IPR number in the popup window?
Currently, most prophage detection programs can only be run using command-line interface. There are only 2 or 3 that can be done on other web servers. This particular tool takes raw genomic sequences, which will be very helpful for our current CF project. I placed two links to both the source code, and the paper describing how the program works.
https://academic.oup.com/bioinformatics/advance-article/doi/10.1093/bioinformatics/btaa250/582287
https://github.com/bobeobibo/phigaro
We need good genome mapping tools. When someone can fit this in, the follow tools need to be tested and further developed.
(1) Our current genome mapper tool is crude and the output needs heavy editing in imaging software. It would be nice to refine the output so that the output can be more directly usable. When someone can fit this in, we can discuss the ideal output look.
(2) X-vis also need to be polished so that the output is more defined
(3) Circos tools (PSM prep and PSM plotter, PSM comparison table) need to be checked to see if they still function at all (there should have been at least some bug reports associated with these tools in the past several months)
Somewhere the this repo got out of sync with our private Github Enterprise repo. Need to rebase and merge
Karthik and I are studying the LydA-LydB holin-antiholin proteins of phage P1. These genes are always adjacent.
I need a tool that takes a protein record, finds the associated nucleotide record and then pulls the CDS (aa) sequence from the adjacent CDS, either upstream or downstream. Ideally it would ask for upstream or downstream and in the perfect world, ask how many adjacent CDSs to fetch. (i.e., 2 upstream, 3 downstream, maybe option for both.)
Need of course doesnt mean it is possible.
As I understand it there may be more than one nt record for a protein record but that is ok. It could just go to the top one, fetch the adjacent CDS according to spec, and then report the locus tag of the nt record accessed.
<repeat>
blocks in prep, use <input multiple="True">
Galaxy Tool Wrapper for the ProphET tool requested by Ryland Young
k7
Refresh your history ~20 times and you will receive a red error box. Pretty innocuous, but can be annoying
When you create a gene feature, an extra CDS appears around the SD sequence. If you right click at the first base of the gene to select translation start, this can be fixed.
good one is 'tRNA and tmRNA' and bad one is 'Aragorn'
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