SUMMARISING RUN PARAMETERS ========================== Input filename: /gscratch/scrubbed/yaaminiv/Manchester/analyses/trimgalore/zr3616_5_R2_val_2.fq.gz Trimming mode: paired-end Trim Galore version: 0.6.6 Cutadapt version: 3.1 Number of cores used for trimming: 1 Quality Phred score cutoff: 20 Quality encoding type selected: ASCII+33 Adapter sequence: 'AGATCGGAAGAGC' (Illumina TruSeq, Sanger iPCR; user defined) Maximum trimming error rate: 0.1 (default) Minimum required adapter overlap (stringency): 1 bp Minimum required sequence length for both reads before a sequence pair gets removed: 20 bp Running FastQC on the data once trimming has completed Running FastQC with the following extra arguments: --outdir /gscratch/scrubbed/yaaminiv/Manchester/analyses/trimgalore-2 --threads 28 Output file will be GZIP compressed This is cutadapt 3.1 with Python 3.8.5 Command line parameters: -j 1 -e 0.1 -q 20 -O 1 -a AGATCGGAAGAGC /gscratch/scrubbed/yaaminiv/Manchester/analyses/trimgalore/zr3616_5_R2_val_2.fq.gz Processing reads on 1 core in single-end mode ... Finished in 3400.83 s (23 µs/read; 2.62 M reads/minute). === Summary === Total reads processed: 148,703,891 Reads with adapters: 63,834,369 (42.9%) Reads written (passing filters): 148,703,891 (100.0%) Total basepairs processed: 14,313,656,899 bp Quality-trimmed: 15,779,438 bp (0.1%) Total written (filtered): 14,225,303,648 bp (99.4%) === Adapter 1 === Sequence: AGATCGGAAGAGC; Type: regular 3'; Length: 13; Trimmed: 63834369 times No. of allowed errors: 1-9 bp: 0; 10-13 bp: 1 Bases preceding removed adapters: A: 45.0% C: 10.8% G: 7.3% T: 37.0% none/other: 0.0% Overview of removed sequences length count expect max.err error counts 1 57873635 37175972.8 0 57873635 2 3899292 9293993.2 0 3899292 3 1371063 2323498.3 0 1371063 4 679337 580874.6 0 679337 5 6129 145218.6 0 6129 6 1562 36304.7 0 1562 7 607 9076.2 0 607 8 132 2269.0 0 132 9 850 567.3 0 53 797 10 1426 141.8 1 17 1409 11 269 35.5 1 0 269 12 59 8.9 1 0 59 13 6 2.2 1 0 6 17 1 2.2 1 0 1 63 1 2.2 1 0 1 RUN STATISTICS FOR INPUT FILE: /gscratch/scrubbed/yaaminiv/Manchester/analyses/trimgalore/zr3616_5_R2_val_2.fq.gz ============================================= 148703891 sequences processed in total Total number of sequences analysed for the sequence pair length validation: 148703891 Number of sequence pairs removed because at least one read was shorter than the length cutoff (20 bp): 147339 (0.10%)