IsoQuant 3.6

Full IsoQuant documentation can found here. Information in this README is given only for convenience and is not a full user manual.

Citation information
Feedback and bug reports
Quick start examples

About IsoQuant

IsoQuant is a tool for the genome-based analysis of long RNA reads, such as PacBio or Oxford Nanopores. IsoQuant allows to reconstruct and quantify transcript models with high precision and decent recall. If the reference annotation is given, IsoQuant also assigns reads to the annotated isoforms based on their intron and exon structure. IsoQuant further performs annotated gene, isoform, exon and intron quantification. If reads are grouped (e.g. according to cell type), counts are reported according to the provided grouping.

Latest IsoQuant version can be downloaded from github.com/ablab/IsoQuant/releases/latest.

Full IsoQuant documentation is available at ablab.github.io/IsoQuant.

Supported sequencing data

IsoQuant support all kinds of long RNA data:

PacBio CCS
ONT dRNA / ONT cDNA
Assembled / corrected transcript sequences

Reads must be provided in FASTQ or FASTA format (can be gzipped). If you have already aligned your reads to the reference genome, simply provide sorted and indexed BAM files. IsoQuant expect reads to contain polyA tails. For more reliable transcript model construction do not trim polyA tails.

IsoQuant can also take aligned Illumina reads to correct long-read spliced alignments. However, short reads are not used to discover transcript models or compute abundances.

Supported reference data

Reference genome is mandatory and should be provided in multi-FASTA format (can be gzipped).

Reference gene annotation is not mandatory, but is likely to increase precision and recall. It can be provided in GFF/GTF format (can be gzipped).

Pre-constructed minimap2 index can also be provided to increase mapping time.

Citation

The paper describing IsoQuant algorithms and benchmarking is available at 10.1038/s41587-022-01565-y.

To try IsoQuant you can use the data that was used in the publication zenodo.org/record/7611877.

Feedback and bug reports

Your comments, bug reports, and suggestions are very welcome. They will help us to further improve IsoQuant. If you have any troubles running IsoQuant, please send us isoquant.log from the <output_dir> directory.

You can leave your comments and bug reports at our GitHub repository tracker or send them via email: isoquant.rna@gmail.com.

Quick start

Full IsoQuant documentation is available at ablab.github.io/IsoQuant.
IsoQuant can be downloaded from github.com/ablab/IsoQuant or installed via conda:
```
conda create -c conda-forge -c bioconda -n isoquant python=3.8 isoquant
```
If installing manually, you will need Python3 (3.8 or higher), gffutils, pysam, pybedtools, biopython and some other common Python libraries to be installed. See requirements.txt for details. You will also need to have minimap2 and samtools to be in your $PATH variable.
Verify your installation by running:
```
isoquant.py --test
```

To run IsoQuant on raw FASTQ/FASTA files use the following command

isoquant.py --reference /PATH/TO/reference_genome.fasta \
--genedb /PATH/TO/gene_annotation.gtf \
--fastq /PATH/TO/sample1.fastq.gz /PATH/TO/sample2.fastq.gz \
--data_type (assembly|pacbio_ccs|nanopore) -o OUTPUT_FOLDER

For example, using the toy data provided within this repository,

./isoquant.py --reference tests/toy_data/MAPT.Mouse.reference.fasta \
--genedb tests/toy_data/MAPT.Mouse.genedb.gtf \
--fastq tests/toy_data/MAPT.Mouse.ONT.simulated.fastq \
--data_type nanopore -o toy_data_out

To run IsoQuant on aligned reads (make sure your BAM is sorted and indexed) use the following command:

isoquant.py --reference /PATH/TO/reference_genome.fasta \
--genedb /PATH/TO/gene_annotation.gtf \
--bam /PATH/TO/sample1.sorted.bam /PATH/TO/sample2.sorted.bam \
--data_type (assembly|pacbio_ccs|nanopore) -o OUTPUT_FOLDER