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rvolden avatar rvolden commented on August 17, 2024

The splint sequence is fine, but I'm adding splint.fasta with the exact sequence that was used in the paper. I'm also adding adapter.fasta that contains the 3' and 5' adapters used in post processing.
I can supply you with a demultiplexing script if you need one. How are you multiplexing your samples?

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mbosio85 avatar mbosio85 commented on August 17, 2024

Hi,
Thanks a lot for your answer.
If I get it right I will process the ONT data from the 96 samples of B-cells using the splint and adapter you provide. This will generate an output with reads from 96 samples in one single output that will need to be demultiplexed. If you already have a script for those 96 sample I would like to give it a try.

About your question, I don't have my own samples yet, I wanted to try the tool and replicate your results from the paper so I can see the kind of data it outputs (I am actually interested seeing what happens in the percentage of genes with coverage but no isoform detected by Mandalorion II ). Once I am acquainted with the software and data analysis I'll proceed thinking more about the experimental design details.

thanks again!
Mattia

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rvolden avatar rvolden commented on August 17, 2024

Sorry this took a while to get to you, but I've added the indexes and the demultiplexing script to the paper directory on the repo. Let me know if you have any other questions and I'll get back to you faster than last time

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