Find Prokaryotic Genes
The Find Prokaryotic Genes tool allows you to annotate a DNA sequence with CDS information. The tool is currently for use with near-complete single prokaryotic genomic and metagenomic data.
The tool creates a gene prediction model from the input sequence, which estimates GC content, conserved sequences corresponding to ribosomal binding sites, start and stop codon usages, and a statistical model (namely, an Interpolated Markov Model) for estimating the probability of a sequence to be part of a gene compared to the background. The model is then used to predict coding sequences from the input sequence. Note that this tool is inspired by Glimmer 3 (see http://ccb.jhu.edu/papers/glimmer3.pdf).
To maximize the gene prediction accuracy, the gene models should be trained on sequences that belong to the same species or to similar ones. When the input consists of sequences originating from multiple organisms, it is recommended to build a gene model for each organism by choosing the "Learn one gene model for each assembly" option. When this option is chosen, the tool will consider all sequences with the same label in the "Assembly_ID" column as coming from the same organism. The "Assembly_ID" column will be automatically populated when downloading assemblies from the Download Microbial Reference Database tool. When assembly information is not known, for example when the input consists of de novo assembled metagenomics sequences, the Bin Pangenomes by Sequence and Bin Pangenomes by Taxonomy tools can be used to group sequences into bins whose sequences are likely to come from the same organism.
To start the analysis, go to:
Functional Analysis (
) | Find Prokaryotic Genes (
)
In the first dialog, select input sequences. The input should consist of one or few contigs from the same species. If several sequences are provided as input and the "Assembly_ID" annotations are present, the tool will build a separate model for each assembly. The tool can also be run in batch mode.
In the second dialog (figure 14.1), it is possible to configure the tool.
Figure 14.1: Configuring the Find Prokaryotic Genes tool
- Model
- Learn one gene model: Learns a single model from the data. Assumes that the sequences come from one organism or a group of closely related organisms.
- Learn one gene model for each assembly: Learns a model for each assembly or bin. This option should be used for example with the output of Bin Pangenomes by Sequence, which outputs a contig list with their assigned bin listed in the Assembly_ID column. Note that Bin Pangenomes by Taxonomy and Download Microbial Reference Database also creates similar sequence lists with an assigned bin or assembly listed in the Assembly_ID column. In this case, one can run the tool independently on each bin.
- Use a previously trained model and use its default parameters: This option allows to choose a model that has been previously trained and run the analysis with the same parameters used when training the model.
- Use a previously trained model: This option allows to choose a model that has been previously trained. It also allows to modify some parameters.
In all but one of this option, the following parameters can be modified:
- Minimum gene length: in bp, excluding start and stop codons.
- Maximum gene overlap: in bp
- Minimum score: Putative genes with a score below this value will be ignored. The value of a gene score depends on how well the sequence of the gene matches the model. It is computed by taking into account how much the sequence is typical of a coding region (as opposed to background noise or the same coding region read in a different frame), of the prevalence of the start codon, and of the presence of a putative ribosomal binding site near the start codon.
- Open ended sequence: check this option to annotate open-ended sequences, which is particularly useful for annotating small contigs.
- Genetic Code
The genetic code to use (default to bacterial). This genetic code is used to determine which stop codons should be used and to compute a background distribution for amino-acid usage.
- Output annotations Delete Existing CDS and Gene Annotations. This is selected by default in order to avoid having many duplicate annotations. Unchecking is useful if one wants to compare the results with other annotations.
The tool will output a copy of the input sequence with CDS and Gene annotations. It is possible to Save the gene model(s) used for the analysis when the one of the options "Learn one gene model" was selected earlier. This model can then be reused to annotate other input sequences by setting the "Model Training" option to "Use a previously trained model" or "Use a previously trained model and use its default parameters".