TranscriptClean is a Python program that corrects mismatches, microindels, and noncanonical splice junctions in long reads that have been mapped to the genome. It is designed for use with sam files from the PacBio Iso-seq and Oxford Nanopore transcriptome sequencing technologies. A variant-aware mode is available for users who want to avoid correcting away known variants in their data.
Note: At the present time, TranscriptClean does not work on SAM files that use X/= operators rather than M to represent matches in the CIGAR field. We are working on adding support for this in a future version.
To install, clone this repo and install using pip:
git clone git@github.com:mortazavilab/TranscriptClean.git
cd TranscriptClean
pip install -e .In addition, R (tested with v.3.3.2) is needed to run the visualization script, generate_report.R.
TranscriptClean is run from the command line as follows. Please note that releases 2.0+ can be run in multithreaded fashion. For fastest performance, we recommend sorting your input SAM file. For additional details and examples, please see the Wiki section.
transcriptclean --sam transcripts.sam --genome hg38.fa --outprefix /my/path/outfile
| Option | Shortcut | Description |
|---|---|---|
| --help | -h | Print a list of the input options with descriptions |
| --sam | -s | Input sam file (mandatory). The aligner used to create it must be splice aware if you want to correct splice junctions. |
| --genome | -g | Reference genome fasta file (mandatory). Should be the same one used during alignment to generate the sam file. |
| --threads | -t | Number of threads to run program with. Default = 1. |
| --outprefix | -o | Prefix for the output files. Default = "out". |
| Option | Shortcut | Description |
|---|---|---|
| --dryRun | n/a | Include this option to run an inventory of all indels in the data without performing any correction. Useful for selecting maxLenIndel and maxSJOffset size |
| --correctMismatches | -m | If set to false, TranscriptClean will skip mismatch correction. Default = True. |
| --correctIndels | -i | If set to false, TranscriptClean will skip indel correction. Default = True. |
| --variants | -v | Optional: VCF-formatted file of variants to avoid correcting (this enables variant-aware correction). Irrelevant if correctMismatches is set to false. |
| --spliceJns | -j | High-confidence splice junction file obtained by mapping Illumina short reads to the genome using STAR. More formats may be supported in the future. This file is necessary if you want to correct noncanonical splice junctions. |
| --maxLenIndel | n/a | Maximum size indel to correct. Default = 5 bp. |
| --maxSJOffset | n/a | Maximum distance from annotated splice junction to correct. Default = 5 bp. |
| --primaryOnly | n/a | If this option is set, TranscriptClean will only output primary mappings of transcripts (ie it will filter out unmapped and multimapped lines from the SAM input.) |
| --canonOnly | n/a | If this option is set, TranscriptClean will only output transcripts that are either canonical or that contain annotated noncanonical junctions to the clean SAM and Fasta files at the end of the run. |
| Option | Shortcut | Description |
|---|---|---|
| --tmpDir | n/a | If you would like the tmp files to be written somewhere different than the final output, provide the path to that location here. For example, a tmp directory on the local drive of a compute node. |
| --bufferSize | n/a | Number of lines to output to file at once by each thread during run. Default = 100 |
| --deleteTmp | n/a | If this option is set, the temporary directory generated by TranscriptClean (TC_tmp) will be removed at the end of the run. |
TranscriptClean outputs the following files:
Please cite our paper when using TranscriptClean:
Dana Wyman, Ali Mortazavi, TranscriptClean: variant-aware correction of indels, mismatches and splice junctions in long-read transcripts, Bioinformatics, Volume 35, Issue 2, 15 January 2019, Pages 340–342, https://doi.org/10.1093/bioinformatics/bty483