CRISPResso version 2.3.1
[Command used]:
/software/EasyBuild/Intel_Xeon_Platinum_8358_CPU__2.60GHz/software/crispresso2/2.3.1/bin/CRISPResso -o /mmfs1/projects/rrc_shared/common/practice_data/CRISPresso/gchlip2_20260708_work/crispresso_out/CRISPRessoBatch_on_crispresso_batch --name Sample009 --exclude_bp_from_left 15 --needleman_wunsch_gap_open -20 --exclude_bp_from_right 15 --min_single_bp_quality 0 --conversion_nuc_to T --aln_seed_len 10 --min_paired_end_reads_overlap 10 --max_paired_end_reads_overlap None --needleman_wunsch_gap_extend -2 --quantification_window_size 1 --n_processes 6 --needleman_wunsch_gap_incentive 1 --prime_editing_gap_open_penalty -50 --flash_command None --verbosity 3 --amplicon_name Reference --plot_window_size 20 --quantification_window_center -3 --prime_editing_pegRNA_extension_quantification_window_size 5 --min_average_read_quality 0 --fastp_command fastp --prime_editing_pegRNA_scaffold_min_match_length 1 --max_rows_alleles_around_cut_to_plot 50 --amplicon_seq TAAACTACCAGAAGTATCAGTGCTAAAAGTATCCTTTTCTTTCCTACAGATTCCTCCTTATGGCCAACAAGGCCCCAGCGGGTATGGTCAGCAGGGCCAGACTCCATATTACAACCAGCAAAGTCCTCACCCCCAGCAGCAGCAGCCACCCTACTCTCAGCAACCACCATCCCAGACCCCTCATGCTCAACCTTCATATCAGCAGCAGCCTCAGTCTCAGCCACCACAGCTCCAGTCATCTCAGCCTCCATATTCCCAGCAGCCA --flexiguide_homology 80 --trimmomatic_command None --default_min_aln_score 60 --fastq_r1 Sample009_R1.fastq.gz --aln_seed_count 5 --aln_seed_min 2 --guide_seq GGACTTTGCTGGTTGTAATA --needleman_wunsch_aln_matrix_loc EDNAFULL --config_file None --min_bp_quality_or_N 0 --flexiguide_seq None --conversion_nuc_from C --min_frequency_alleles_around_cut_to_plot 0.2 --fastq_r2 Sample009_R2.fastq.gz --prime_editing_gap_extend_penalty 0

[Execution log]:
Computing quantification windows
CRISPRessoPro not installed
Added 0 guides with flexible matching
	Original flexiguides: ['None']
	Found guides: []
	Mismatch locations: []
Processing sequences with fastp...
Read1 before filtering:
total reads: 9070
total bases: 1387452
Q20 bases: 1336468(96.3254%)
Q30 bases: 1321760(95.2653%)

Read2 before filtering:
total reads: 9070
total bases: 1387398
Q20 bases: 1352730(97.5012%)
Q30 bases: 1338260(96.4583%)

Merged and filtered:
total reads: 8830
total bases: 2235547
Q20 bases: 2175197(97.3004%)
Q30 bases: 2155790(96.4323%)

Filtering result:
reads passed filter: 18140
reads failed due to low quality: 0
reads failed due to too many N: 0
reads corrected by overlap analysis: 620
bases corrected by overlap analysis: 851

Duplication rate: 82.4807%

Insert size peak (evaluated by paired-end reads): 254

Read pairs merged: 8830
% of original read pairs: 97.3539%
% in reads after filtering: 100%


JSON report: /mmfs1/projects/rrc_shared/common/practice_data/CRISPresso/gchlip2_20260708_work/crispresso_out/CRISPRessoBatch_on_crispresso_batch/CRISPResso_on_Sample009/fastp_report.json
HTML report: /mmfs1/projects/rrc_shared/common/practice_data/CRISPresso/gchlip2_20260708_work/crispresso_out/CRISPRessoBatch_on_crispresso_batch/CRISPResso_on_Sample009/fastp_report.html

fastp -i Sample009_R1.fastq.gz -I Sample009_R2.fastq.gz --merge --merged_out /mmfs1/projects/rrc_shared/common/practice_data/CRISPresso/gchlip2_20260708_work/crispresso_out/CRISPRessoBatch_on_crispresso_batch/CRISPResso_on_Sample009/oet.extendedFrags.fastq.gz --unpaired1 /mmfs1/projects/rrc_shared/common/practice_data/CRISPresso/gchlip2_20260708_work/crispresso_out/CRISPRessoBatch_on_crispresso_batch/CRISPResso_on_Sample009/out.notCombined_1.fastq.gz --unpaired2 /mmfs1/projects/rrc_shared/common/practice_data/CRISPresso/gchlip2_20260708_work/crispresso_out/CRISPRessoBatch_on_crispresso_batch/CRISPResso_on_Sample009/out.notCombined_2.fastq.gz --overlap_len_require 10 --thread 6 --json /mmfs1/projects/rrc_shared/common/practice_data/CRISPresso/gchlip2_20260708_work/crispresso_out/CRISPRessoBatch_on_crispresso_batch/CRISPResso_on_Sample009/fastp_report.json --html /mmfs1/projects/rrc_shared/common/practice_data/CRISPresso/gchlip2_20260708_work/crispresso_out/CRISPRessoBatch_on_crispresso_batch/CRISPResso_on_Sample009/fastp_report.html --disable_adapter_trimming --disable_trim_poly_g --disable_quality_filtering --disable_length_filtering 
fastp v0.23.4, time used: 1 seconds
Done!
Done!
Aligning sequences...
Processing reads; N_TOT_READS: 0 N_COMPUTED_ALN: 0 N_CACHED_ALN: 0 N_COMPUTED_NOTALN: 0 N_CACHED_NOTALN: 0
Finished reads; N_TOT_READS: 8830 N_COMPUTED_ALN: 1154 N_CACHED_ALN: 7635 N_COMPUTED_NOTALN: 24 N_CACHED_NOTALN: 17
Done!
Quantifying indels/substitutions...
Done!
Calculating allele frequencies...
Done!
Saving processed data...
Making Plots...
Plotting read bar plot
Plotting read class pie chart and bar plot
Begin processing plots for amplicon Reference
Plotting nucleotide quilt across amplicon
Plotting nucleotide distribuition around sgRNA GGACTTTGCTGGTTGTAATA for Reference
Plotting indel size distribution for Reference
Plotting frequency deletions/insertions for Reference
Plotting amplication modifications for Reference
Plotting modification frequency for Reference
Plotting quantification window locations for Reference
Plotting position dependent indel for Reference
Plotting allele distribution around cut for Reference
Done!
Done!
Removing Intermediate files...
 Low number of total reads: <10000. Total reads: 8830.
 >=1.0% of reads have modifications at the start or end. Total reads: 8789, Irregular reads: 227.
 >=0.2% of substitutions were outside of the quantification window. Total substitutions: 3464, Substitutions outside window: 3464.
Analysis Complete!