isONcorrect is a tool for error-correcting Oxford Nanopore cDNA reads. It is designed to handle highly variable coverage and exon variation within reads and achieves about a 0.5-1% median error rate after correction. It leverages regions shared between reads from different isoforms achieve low error rates even for low abundant transcripts. See paper for details.
Update: Since v0.0.8, isONcorrect uses different default parameters compared to what was used in the paper. The new parameters make isONcorrect 2-3 times faster and use 3-8 times less memory with only a small cost of increased median post-correction error rate. With the new parameter setting the correction accuracy is 98.5-99.3% instead of 98.9–99.6% on the data used in the paper. Current default uses --k 9 --w 20 --max_seqs 2000. To invoke settings used in paper, set parameters --k 9 --w 10 --max_seqs 1000.
Processing and error correction of full-length ONT cDNA reads is achieved by the pipeline of running pychopper --> isONclust --> isONcorrect. All these steps can be run in one go with this script. See below for installation and usage.
isONcorrect is distributed as a python package supported on Linux / OSX with python v>=3.4. 
Typical install time on a desktop computer is about 10 minutes with conda for this software.
Conda is the preferred way to install isONcorrect.
- Create and activate a new environment called isoncorrect
conda create -n isoncorrect python=3 pip
conda activate isoncorrect
- Install isONcorrect and its dependency
spoa.
pip install isONcorrect
conda install -c bioconda spoa
- You should now have 'isONcorrect' installed; try it:
isONcorrect --help
Upon start/login to your server/computer you need to activate the conda environment "isonclust" to run isONcorrect as:
conda activate isoncorrect
- You probably want to install
pychopperandisONclustin the isoncorrect environmment as well to run the complete correction pipeline if you haven't already. This can be done with:
pip install isONclust
conda install -c bioconda "hmmer>=3.0"
conda install -c bioconda "pychopper>=2.0"
You are now set to run the correction_pipeline. See USAGE.
pip is pythons official package installer and is included in most python versions. If you do not have pip, it can be easily installed from here and upgraded with pip install --upgrade pip.
To install isONcorrect, run:
pip install isONcorrect
Then install spoa and include it in your path.
Make sure the below listed dependencies are installed (installation links below). Versions in parenthesis are suggested as isONcorrect has not been tested with earlier versions of these libraries. However, isONcorrect may also work with earliear versions of these libaries.
In addition, please make sure you use python version >=3.
With these dependencies installed. Run
git clone https://github.com/ksahlin/isONcorrect.git
cd isONcorrect
./isONcorrectYou can verify successul installation by running isONcorrect on this small dataset of 100 reads. Assuming you have cloned this repository and the repository is found in /my/path/isONcorrect, simply run:
isONcorrect --fastq /my/path/isONcorrect/test_data/isoncorrect/0.fastq \
--outfolder [output path]
Expected runtime for this test data is about 15 seconds. The output will be found in [output path]/corrected_reads.fastq where the 100 reads have the same headers as in the original file, but with corrected sequence. Testing the paralleized version (by separate clusters) of isONcorrect can be done by running
./run_isoncorrect --t 3 --fastq_folder /my/path/isONcorrect/test_data/isoncorrect/ \
--outfolder [output path]
This will perform correction on 0.fastq and 1.fastq in parallel. Expected runtime for this test data is about 15 seconds. The output will be found in [output path]/0/corrected_reads.fastq and [output path]/1/corrected_reads.fastq where the 100 reads in each separate cluster have the same headers as in the respective original files, but with corrected sequence.
You can simply run ./correction_pipeline.sh <raw_reads.fq> <outfolder> <num_cores> which will perform the steps 1-5 below for you. The correction_pipeline.sh script is available in this repository here. Simply download the reposotory or the individual correction_pipeline.sh file.
For a fastq file with raw ONT cDNA reads, the following pipeline is recommended:
- Produce full-length reads (with pychopper (a.k.a.
cdna_classifier)) - Cluster the full length reads into genes/gene-families (isONclust)
- Make fastq files of each cluster (
isONclust write_fastqcommand) - Correct individual clusters (isONcorrect)
- Join reads back to a single fastq file (This is of course optional)
The contents of the correction_pipeline.sh is (roughly) provided below. If you want more individual control over the steps than what the correction_pipeline.sh can do for you (such as different parameters in each step), you can modify/remove arguments as needed in correction_pipeline.sh or in the below script.
#!/bin/bash
# Pipeline to get high-quality full-length reads from ONT cDNA sequencing
# Set path to output and number of cores
root_out="outfolder"
cores=20
mkdir -p $root_out
cdna_classifier.py raw_reads.fq $root_out/full_length.fq -t $cores
isONclust --t $cores --ont --fastq $root_out/full_length.fq \
--outfolder $root_out/clustering
isONclust write_fastq --N 1 --clusters $root_out/clustering/final_clusters.tsv \
--fastq $root_out/full_length.fq --outfolder $root_out/clustering/fastq_files
run_isoncorrect --t $cores --fastq_folder $root_out/clustering/fastq_files --outfolder $root_out/correction/
# OPTIONAL BELOW TO MERGE ALL CORRECTED READS INTO ONE FILE
touch $root_out/all_corrected_reads.fq
OUTFILES=$root_out"/correction/"*"/corrected_reads.fastq"
for f in $OUTFILES
do
cat $f >> $outfolder/all_corrected_reads.fq
done
isONcorrect does not need ONT reads to be full-length (i.e., produced by pychopper), but unless you have specific other goals, it is advised to run pychopper for any kind of downstream analysis to guarantee full-length reads.
The output of run_isoncorrect is one file per cluster with identical headers to the original reads.
For some datasets, e.g. targeted data, isONclust can produce highly uneven clusters, i.e., a few very large clusters and some/many small ones. In such cases, runtime can be reduced if the argument --split_wrt_batches is specified to run_isoncorrect.
isONcorrect currently supports parallelization across cores on a node (parameter --t), but not across several nodes. There is a way to overcome this limitation if you have access to multiple nodes as follows. The run_isoncorrect step can be parallilized across n nodes by (in bash or other environment, e.g., snakemake) parallelizing the following commands
run_isoncorrect --fastq_folder outfolder/clustering/fastq_files --outfolder /outfolder/correction/ --split_mod n --residual 0
run_isoncorrect --fastq_folder outfolder/clustering/fastq_files --outfolder /outfolder/correction/ --split_mod n --residual 1
run_isoncorrect --fastq_folder outfolder/clustering/fastq_files --outfolder /outfolder/correction/ --split_mod n --residual 2
...
run_isoncorrect --fastq_folder outfolder/clustering/fastq_files --outfolder /outfolder/correction/ --split_mod n --residual n-1
Which tells isONcorrect to only work with distinct cluster IDs.
Please cite [1] when using isONcorrect.
- Sahlin, K., Medvedev, P. Error correction enables use of Oxford Nanopore technology for reference-free transcriptome analysis. Nat Commun 12, 2 (2021). https://doi.org/10.1038/s41467-020-20340-8 Link.
GPL v3.0, see LICENSE.txt.