CRISPResso version 2.3.4 [Command used]: /var/www/webapps/CRISPRessoWEB/.pixi/envs/default/bin/CRISPResso --fastq_r1 base_editor.fastq.gz --amplicon_seq GGCCCCAGTGGCTGCTCTGGGGGCCTCCTGAGTTTCTCATCTGTGCCCCTCCCTCCCTGGCCCAGGTGAAGGTGTGGTTCCAGAACCGGAGGACAAAGTACAAACGGCAGAAGCTGGAGGAGGAAGGGCCTGAGTCCGAGCAGAAGAAGAAGGGCTCCCATCACATCAACCGGTGGCGCATTGCCACGAAGCAGGCCAATGGGGAGGACATCGATGTCACCTCCAATGACTAGGGTGG --guide_seq GAGTCCGAGCAGAAGAAGAA --quantification_window_size 20 --quantification_window_center -10 --base_editor_output --write_cleaned_report --place_report_in_output_folder --use_matplotlib [Execution log]: CRISPRessoPro v1.0.1 installed Computing quantification windows Added 0 guides with flexible matching Original flexiguides: ['None'] Found guides: [] Mismatch locations: [] Counting reads in input Counting reads after preprocessing... Aligning sequences... Finished reading fastq file; 3939 unique reads found of 25000 total reads found Processing Reads; 0 Completed out of 3939 Unique Reads Finished reads; N_TOT_READS: 25000 N_COMPUTED_ALN: 3909 N_CACHED_ALN: 21061 N_COMPUTED_NOTALN: 30 N_CACHED_NOTALN: 0 Done! Quantifying indels/substitutions... Done! Calculating allele frequencies... Done! Saving processed data... Making Plots... Done! Removing Intermediate files... >=1.0% of reads have modifications at the start or end. Total reads: 24970, Irregular reads: 24970. >=0.2% of substitutions were outside of the quantification window. Total substitutions: 17498, Substitutions outside window: 4061. Pro report written to CRISPResso_on_base_editor/CRISPResso2_report.html _ ' ) .-' (____ C)| \ \ / \___/ Analysis Complete!