Thank you for offering a great tool for nanopore scRNA-seq data processing.
I have a few questions regarding the data processing
1. score.mat
in the UMI merging step scores.mat is needed but I cannot find it in this repo and also in C3POa repo
where can I find scores.mat file?
2. preprocessing order
I am following the instructions in the repos and the bioarxiv preprint (Highly Multiplexed Single-Cell Full-Length cDNA Sequencing of human immune cells with 10X Genomics and R2C2)
I am planning to execute the code in the following order.
But I am a little bit confusing since the order of scripts are slightly different between that in this repo's README.md and that in the preprint
Is merger UMI steps should be done before detBarcodes.py or after all the other scripts?
Dear Roger,
Thank you for offering a great tool for nanopore scRNA-seq data processing.
I have a few questions regarding the data processing
1. score.mat
in the UMI merging step scores.mat is needed but I cannot find it in this repo and also in C3POa repo where can I find scores.mat file?
2. preprocessing order
I am following the instructions in the repos and the bioarxiv preprint (Highly Multiplexed Single-Cell Full-Length cDNA Sequencing of human immune cells with 10X Genomics and R2C2)
I am planning to execute the code in the following order.
1) C3POa.py 2) C3POa_postprocessing.py 3) ExtractUMIs.py 4) MergeUMIs.py 5) MergeUMIs10x.py 6) detBarcodes.py 7) Demultiplex_R2C2_reads_kmerBased.py 8) match_fastas.py 9) demux_nano.py 10) make_cell_subreads.py
But I am a little bit confusing since the order of scripts are slightly different between that in this repo's README.md and that in the preprint Is merger UMI steps should be done before detBarcodes.py or after all the other scripts?