Comments (4)
Dan it would be great to see some advancement here on the Fungi - we can collect the sets of examples and use the HMMs from the alignments we have but I am not sure if need to focus on clade-specific sets and iterate or if can be a single HMM sufficient. Would be happy to talk more about how we are approaching this - there are also some efforts from JGI To extract these regions through their pipelines so would be good to connect the dots.
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Hi, much appreciated for the response. Yes, I am still progressing this in collaboration with a colleague. I'd be keen to talk sometime about the specifics of what exactly you'd need to progress this. We have plenty of fungal genomes we can mine :)
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Hi, I'm Brogan McGreal a researcher at Plant and Food Research. Our team focuses on molecular plant pathogen interactions and I work with @danwiththeplan. We are currently looking to produce a fungal gene annotation pipeline using open source tools. We'd be happy to discuss what is required to get things working for fungi. I'm not sure what type of inputs you need and in what format i.e. do you need fungal genomes & aligned rna seq reads etc. As @danwiththeplan mentioned, we have plenty of fungal genomic and transcriptomic data.
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Hi if you are interested in fungal genome annotation I would first point to our project which has been successfully used for hundreds of genomes I've annotated and deposited and many others - https://github.com/nextgenusfs/funannotate/ - Jon has done an incredible job putting together the pipelines and several others are working on embedding it in snakemake or nextflow pipelines to enable more efficient annotation pipelines.
We also have generated and work on several thousand fungal genomes in our projects so it would be useful to explore what is helpful, my experience is the ribosomal loci are often missing from non-long read assemblies that do not account for the high coverage of the regions, so a combination of strategies are needed to actually get the ribosomal loci in an assembly depending on the ratio of their coverage to the nuclear genome and the parameters used.
I think mainly if the issue in this project is to better provide the HMMs to support the ribosomal locus and associated gene extractions it would make sense to match things up with what ITSx does to use the HMMs to find the boundaries and orient the ITS1 and ITS2 https://microbiology.se/software/itsx/.
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Related Issues (20)
- Could the barrnap be used to predict the rrna of *.fna.gz file? HOT 1
- possible option for "prokaryotic" search (archaeal + procaryotic)?
- Overlapping 5.8S and 28S annotations in Eukaryotic rDNAs HOT 4
- Cannot specify a file on cmdline?
- GFF output and Fasta-headers give different start-coordinates of rRNA-genes
- nhmmer failed to run - Error: Invalid alphabet type in target for nhmmer. Expect DNA or RNA HOT 7
- [barrnap] ERROR: nhmmer failed to run HOT 3
- issue with rrna.fa writing and bed tools HOT 2
- calling two overlapping sequences separate partial 16S sequences
- please add option to force overwrite .fai index during, or automatically delete fai file after barrnap run
- barrnap-v0.9 debian package has incomplete database HOT 2
- Fail if Bedtools issues a fasta normalization error
- barrnap doesn't create any output
- barrnap
- Building eukaryotic rrna operon database
- Barrnap (nhmmer) takes an eternity to run HOT 1
- SILVA version? HOT 1
- Error: Invalid alphabet type in target for nhmmer.
- Bug getfasta with --outseq HOT 1
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