SUMMARISING RUN PARAMETERS ========================== Input filename: Geoduck-NMP-gDNA-8_S29_L008_R2_001.fastq.gz Trimming mode: paired-end Trim Galore version: 0.4.4_dev Cutadapt version: 1.16 Quality Phred score cutoff: 20 Quality encoding type selected: ASCII+33 Adapter sequence: 'AGATCGGAAGAGC' (Illumina TruSeq, Sanger iPCR; auto-detected) 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/samwhite/illumina_geoduck_hiseq/20180328_trim_galore_illumina_hiseq_geoduck/20180328_fastqc_trimmed_hiseq_geoduck --threads 28 Output file will be GZIP compressed This is cutadapt 1.16 with Python 2.7.14 Command line parameters: -f fastq -e 0.1 -q 20 -O 1 -a AGATCGGAAGAGC Geoduck-NMP-gDNA-8_S29_L008_R2_001.fastq.gz Running on 1 core Trimming 1 adapter with at most 10.0% errors in single-end mode ... Finished in 0.39 s (37 us/read; 1.62 M reads/minute). === Summary === Total reads processed: 10,428 Reads with adapters: 2,215 (21.2%) Reads written (passing filters): 10,428 (100.0%) Total basepairs processed: 1,167,532 bp Quality-trimmed: 376,873 bp (32.3%) Total written (filtered): 786,368 bp (67.4%) === Adapter 1 === Sequence: AGATCGGAAGAGC; Type: regular 3'; Length: 13; Trimmed: 2215 times. No. of allowed errors: 0-9 bp: 0; 10-13 bp: 1 Bases preceding removed adapters: A: 29.0% C: 28.0% G: 14.3% T: 26.5% none/other: 2.1% Overview of removed sequences length count expect max.err error counts 1 1607 2607.0 0 1607 2 464 651.8 0 464 3 92 162.9 0 92 4 24 40.7 0 24 5 4 10.2 0 4 6 1 2.5 0 1 7 2 0.6 0 2 16 1 0.0 1 1 24 1 0.0 1 1 30 1 0.0 1 0 1 42 1 0.0 1 1 51 2 0.0 1 2 58 1 0.0 1 1 62 1 0.0 1 1 63 1 0.0 1 1 64 1 0.0 1 1 67 3 0.0 1 1 2 68 2 0.0 1 2 69 2 0.0 1 1 1 70 1 0.0 1 0 1 72 1 0.0 1 0 1 117 1 0.0 1 0 1 149 1 0.0 1 0 1 RUN STATISTICS FOR INPUT FILE: Geoduck-NMP-gDNA-8_S29_L008_R2_001.fastq.gz ============================================= 10428 sequences processed in total Total number of sequences analysed for the sequence pair length validation: 10428 Number of sequence pairs removed because at least one read was shorter than the length cutoff (20 bp): 3616 (34.68%)