Open gkurgan opened 4 years ago
Hi Gavin -
knock-knock currently expects each FASTQ to contain a single amplicon target. To analyze the data you describe, you could preprocess your data to demultiplex each FASTQ into separate files for each target, then feed these demultiplexed files into knock-knock. I would be interested in adding built-in support for this kind of demultiplexing - if you are willing to share some example data, send me an email at jeff.hussmann@gmail.com. Thanks!
Hello!
I just had a quick question. Looking through the documentation I am a little unclear if knock-knock can be used to analyze CRISPR NGS data generated using multiplexed PCR (e.g. multiple amplicon targets in a single FASTQ). This is mainly useful for simultaneous on/off-target analysis of CRISPR editing. Could you possibly provide some clarification regarding this or possibly an example of how it should be used in this case?
Thanks!