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Part 3: Gene prediction

You need to have gone through Part 2: Genome assembly before starting this practical.

Many tools exist for gene prediction, some based on ab initio statistical models of what a protein-coding gene should look like, others that use similarity with protein-coding genes from other species, and others (such as Augustus and SNAP), that use both. There is no perfect tool or approach, thus we typically run many gene-finding tools and call a consensus between the different predicted gene models. MAKER, BRAKER and JAMg can do this for us. Let's use MAKER on a sandbox example.

Running Maker

Create a new main directory for today's practical (e.g., 2020-10-xx-gene_prediction) as well as the input, tmp, and results subdirectories and a WHATIDID.txt file to log your commands. Link the output (assembly) from yesterday's practical into input subdirectory:

cd ~/2020-10-xx-gene_prediction
ln -s ~/2020-09-xx-assembly/results/scaffolds.fasta input/

Pull out the longest few scaffolds from scaffolds.fasta into a new file:

seqtk seq -L 10000 input/scaffolds.fasta > tmp/min10000.fa

Next, cd to your tmp/ folder and run maker -OPTS. This will generate an empty maker_opts.ctl configuration file (ignore the warnings). Edit that file using a text editor such as nano or vim to specify:

We deactivated RepeatMakser and RepeatRunner due to computational constraints as well as the lack of a suitable repeat library. For a real project, we would include RepeatMasker, perhaps after creating a new repeat library.

For a real project, we would also include gene expression data (RNAseq improves gene prediction performance tremendously), protein sequences from related species, and iteratively train gene prediction algorithms (e.g., Augustus and SNAP) for our data.

Finally, run maker maker_opts.ctl. This may take a few minutes, depending on how much data you gave it.

Genome annotation software like MAKER usually provide information about the exon-intron structure of the genes (e.g., in GFF3 format), and sequence of corresponding messenger RNA and protein products (e.g., in FASTA format).

While MAKER is running, make a note of the different file formats you have encountered by now. Which type of data do each file formats contain? Do you understand the difference between the different file formats and data types?

Once MAKER is done the results will be hidden in subdirectories of min10000.maker.output. MAKER provides a helper script to collect this hidden output in one place (again please ignore the warnings for these steps):

# Pull out information about exon-intron structure of the predicted genes. This
# will be saved to the file min10000.all.gff.
gff3_merge -d min10000.maker.output/min10000_master_datastore_index.log

# Pull out predicted messenger RNA and protein sequences. These will be saved
# to the files: min10000.all.maker.augustus.transcripts.fasta, and
# min10000.all.maker.augustus.proteins.fasta
fasta_merge -d min10000.maker.output/min10000_master_datastore_index.log

Quality control of individual genes

So now we have some gene predictions... how can we know if they are any good? The easiest way to get a feel for this is to use the following example sequences: predicted protein sequences from rice and honeybee. We will compare them using BLAST to known sequences from other species in the uniref50 database.

Running BLAST

We will use SequenceServer to run BLAST. Open http://blast.genomicscourse.com/sequenceserver/ in your browser, paste the example rice and honeybee protein sequences in the textbox and click on the 'BLAST' button to run a BLAST search. THIS WILL TAKE A MINUTE or TWO

Now, looking at the BLAST results ask yourself the following questions: Do any of the gene predictions have significant similarity to known sequences? For a given gene prediction, do you think it is complete, or can you infer from the BLAST alignments that something may be wrong? Start by comparing the length of your gene prediction to that of the BLAST hits. Is your gene prediction considerably longer or considerably shorter than BLAST hits? Why?

Now try a few of your gene predictions. BLAST only a maximum of 12 sequences at a time (instead of simply selecting the first 12 genes in your file, copy-paste sequences randomly from the file).

As you can see, gene prediction software is imperfect – this is even the case when using all available evidence. This is potentially costly for analyses that rely on gene predictions - i.e. many of the analyses we might want to do!

“Incorrect annotations [ie. gene identifications] poison every experiment that makes use of them. Worse still the poison spreads.”Yandell & Ence (2012).

Using GeneValidator

The GeneValidator tool can help to evaluate the quality of a gene prediction by comparing features of a predicted gene to similar database sequences. This approach expects that similar sequences should for example be of similar length. Genevalidator was built to automate the comparison of sequence characteristics in a manner similar to what we just did through visual individual BLAST results.

Try to run the example rice and honeybee protein sequences through GeneValidator: http://blast.genomicscourse.com/genevalidator/

Comparing whole genesets & prioritizing genes for manual curation

Genevalidator's visual output can be handy when looking at few genes. But the tool also provides tab-delimited output, useful when working in the command-line or running the software on whole proteomes. This can help analysis:

Manual curation

Because automated gene predictions aren't perfect, manual inspection and fixing is often required. The most commonly used software for this is Apollo/WebApollo.

We won't curate any gene models as part of this practical, but you can learn about it through these youtube videos:

  1. EMBL-ABR training 20171121 - Genome Annotation using Apollo
  2. The i5k : a pan-Arthropoda genome database

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