Closed frankbioinfo closed 6 years ago
We don't support reads aligned through BWA so I am not sure what I am looking at. You should use CRISPResso with paired end reads in fastq format. I suggest you to read carefully the paper (http://rdcu.be/jgvL) and supplementary material: https://www.readcube.com/articles/supplement?doi=10.1038%2Fnbt.3583&index=0&ssl=1&st=f5e8a734a3bfafe4c31a97f8993f72d1&preview=1 where we explain in detail the required inputs, parameters and the different tools.
The plot 4b.usingbam.pdf looks more reasonable to me.
Regards,
Luca
hello Developer,
Thank you for developing this tool.
I am not sure which module should I use for my purpose, we have crispr guided to a target region. we then sequenced the genomic dna (pcr product) that targets this region using miseq 2x250 + 10bp Index1 + 8bp Index2 I used two two different approach
I have attached plots from both the steps, having difficulty in understanding the plots. could you please help in this?
4b.usingbam.pdf 4b.usingfastq.pdf