CRISPResso2
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Analysis of deep sequencing data for rapid and intuitive interpretation of genome editing experiments
I ran this command and it gave me CRISPRessoPooled -r1 TREATED_R1.fastq.gz -r2 TREATED_R2.fastq.gz -f crispressoexp_config.txt -x Genomes/hg38/genome --name AMPLICONS_AND_GENOME --gene_annotations gencodev41.gz --debug and it gave me this error INFO @...
I run CRISPResso2 on command line but it appeared to time out before completion. I did not get all of the typical output files. Could it be that the fast...
Hi! I am running CRISPResso with two fastq files, an amplicon input, gRNA input, and some specific paramters. I get this error when I run --bam_output with the --debug flag....
Hi all, I did an PE screen where I have more than one edit induced in the same sequence. So this means I have one amplicon as reference but more...
Adding verbosity control & sample annotation to the error message for parallel command line run.
**Is your feature request related to a problem? Please describe.** For base editors, fisher's exact test for all substitution doesn't work when I'm interested in specific base substitution. **Describe the...
**Is your feature request related to a problem? Please describe.** I would like to be able to run CRISPResso2 on amplicon ranging from 1,000 - 2,000 bp
The algorithm runs the unit tests successfully now, I imagine that it needs to be integrated into the core so that the newly aligned reads are actually used, right? If...
Hi, I'm running CRISPResso2 in mixed mode and for some samples it is not able to generate index file for the bam alignment and in turn it does not generate...
Hi. Thanks for a great pipeline! I have a population of cells where cells with two different knock-in single nucleotide substitutions are present amongst unedited cells. I would like to...