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Implemented the simulation of CAGE-seq orthogonal data (--CAGE) when running SQANTI-SIM in sample mode.
Added PacBio long read simulation using PBSIM3 (--pbsim).
Added the full-sim mode, which executes the classif, design and sim modules, allowing users to run the complete simulation with just one simple instruction.
Provided pre-trained models and characterized datasets of the WTC11 human cell line.
Updated pre-trained NanoSim models with WTC11 human cell line dRNA and cDNA data. Additionally, users have the option to utilize their specific pre-trained NanoSim models using the --nanosim_model parameter.
Enhanced the --diff_exp parameter by deprecating --low_prob and --high_prob. Now, --diff_exp is a numeric value that allows users to adjust with a single parameter the bias of known and novel expression levels.
Updated SQANTI-SIM evaluation report style.
馃悰 Bug Fixes and Minor Changes
Added the option --expr_file to provide an expression distribution file to sqanti-sim.py design sample to avoid mapping the same reads in different executions.
When using the --long_reads option in sqanti-sim.py design sample mode, SQANTI-SIM now generates an expression file named "sqanti-sim_expression.tsv." This file can be reused in future executions using --expr_file.
Added a default number of novel transcripts to simulate when the user does not specify any.
Added additional example files, providing users with practical examples.
Updated the classification algorithm to the latest SQANTI3 release, version 5.1.2, ensuring up-to-date transcript classification results.
Updated the sqanti-sim.py design sample random expression sampling by implementing inverse transform sampling from ECDFs.
Fixed Partial True Positives (PTP) and Positive Detection Rate (PDR) metrics to consider only non-redundant transcript models.
Fixed conda environment installation issues related to bcbio-gff and updated dependencies.
Fixed SQANTI-SIM Report generating empty tables when not all structural categories were detected.