Bowtie 2 seems to be working fine (tested command 'bowtie2 --version' [2.5.4]) Output format is BAM (default) Alignments will be written out in BAM format. Samtools found here: '/srlab/programs/samtools-1.20/samtools' Reference genome folder provided is ../../data/genome/ (absolute path is '/mmfs1/gscratch/scrubbed/sr320/github/ceasmallr/data/genome/)' FastQ format assumed (by default) Processing sequences up to read no. 10000 from the input file Attention: early reports suggested that high values of -p to have diminishing returns. Please test different values using a small subset of data for your hardware setting. Each Bowtie 2 instance is going to be run with 8 threads. Please monitor performance closely and tune down if necessary! Input files to be analysed (in current folder '/mmfs1/gscratch/scrubbed/sr320/github/ceasmallr/output/04.2-bismark-align'): ../../data/EF06-EM06-Larvae_R1_001.fastp-trim.20220827.fq.gz ../../data/EF06-EM06-Larvae_R2_001.fastp-trim.20220827.fq.gz Library was specified to be not strand-specific (non-directional), therefore alignments to all four possible bisulfite strands (OT, CTOT, OB and CTOB) will be reported Output will be written into the directory: /mmfs1/gscratch/scrubbed/sr320/github/ceasmallr/output/04.2-bismark-align/EF06-EM06-Larvae_score_L0-0.4/ Setting parallelization to single-threaded (default) Summary of all aligner options: -q --score-min L,0,-0.4 -p 8 --reorder --ignore-quals --no-mixed --no-discordant --dovetail --maxins 500 Current working directory is: /mmfs1/gscratch/scrubbed/sr320/github/ceasmallr/output/04.2-bismark-align Now reading in and storing sequence information of the genome specified in: /mmfs1/gscratch/scrubbed/sr320/github/ceasmallr/data/genome/ Single-core mode: setting pid to 1 Paired-end alignments will be performed ======================================= The provided filenames for paired-end alignments are ../../data/EF06-EM06-Larvae_R1_001.fastp-trim.20220827.fq.gz and ../../data/EF06-EM06-Larvae_R2_001.fastp-trim.20220827.fq.gz Input files are in FastQ format Processing reads up to sequence no. 10000 from ../../data/EF06-EM06-Larvae_R1_001.fastp-trim.20220827.fq.gz Writing a C -> T converted version of the input file EF06-EM06-Larvae_R1_001.fastp-trim.20220827.fq.gz to EF06-EM06-Larvae_R1_001.fastp-trim.20220827.fq.gz_C_to_T.fastq Writing a G -> A converted version of the input file EF06-EM06-Larvae_R1_001.fastp-trim.20220827.fq.gz to EF06-EM06-Larvae_R1_001.fastp-trim.20220827.fq.gz_G_to_A.fastq Created C -> T as well as G -> A converted versions of the FastQ file EF06-EM06-Larvae_R1_001.fastp-trim.20220827.fq.gz (10001 sequences in total) Processing reads up to sequence no. 10000 from ../../data/EF06-EM06-Larvae_R2_001.fastp-trim.20220827.fq.gz Writing a C -> T converted version of the input file EF06-EM06-Larvae_R2_001.fastp-trim.20220827.fq.gz to EF06-EM06-Larvae_R2_001.fastp-trim.20220827.fq.gz_C_to_T.fastq Writing a G -> A converted version of the input file EF06-EM06-Larvae_R2_001.fastp-trim.20220827.fq.gz to EF06-EM06-Larvae_R2_001.fastp-trim.20220827.fq.gz_G_to_A.fastq Created C -> T as well as G -> A converted versions of the FastQ file EF06-EM06-Larvae_R2_001.fastp-trim.20220827.fq.gz (10001 sequences in total) Input files are EF06-EM06-Larvae_R1_001.fastp-trim.20220827.fq.gz_C_to_T.fastq and EF06-EM06-Larvae_R1_001.fastp-trim.20220827.fq.gz_G_to_A.fastq and EF06-EM06-Larvae_R2_001.fastp-trim.20220827.fq.gz_C_to_T.fastq and EF06-EM06-Larvae_R2_001.fastp-trim.20220827.fq.gz_G_to_A.fastq (FastQ) Now running 4 individual instances of Bowtie 2 against the bisulfite genome of /mmfs1/gscratch/scrubbed/sr320/github/ceasmallr/data/genome/ with the specified options: -q --score-min L,0,-0.4 -p 8 --reorder --ignore-quals --no-mixed --no-discordant --dovetail --maxins 500 Now starting a Bowtie 2 paired-end alignment for CTread1GAread2CTgenome (reading in sequences from EF06-EM06-Larvae_R1_001.fastp-trim.20220827.fq.gz_C_to_T.fastq and EF06-EM06-Larvae_R2_001.fastp-trim.20220827.fq.gz_G_to_A.fastq, with the options: -q --score-min L,0,-0.4 -p 8 --reorder --ignore-quals --no-mixed --no-discordant --dovetail --maxins 500 --norc)) Found first alignment: GWNJ-1012:512:GW210315000:4:1101:26178:1047_1:N:0:CCAAGTCT+TCATCCTT/1 77 * 0 0 * * 0 0 ANATTATTAATATAATTTTTTAATTATTTAATTTTTTATTATTTATAATTATATATATTTTTTTTTAATTAAATATATAAAAAAAAGTTGGATTAATTAGAAAA F#FFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFF:FFFFFFFFFFFFFFFFFF YT:Z:UP GWNJ-1012:512:GW210315000:4:1101:26178:1047_2:N:0:CCAAGTCT+TCATCCTT/2 141 * 0 0 * * 0 0 TTTTCTAATTAATCCAACTTTTTTTTATATATTTAATTAAAAAAAAATATATATAATTATAAATAATAAAAAATTTAATAATTATAAAATTATATTTATTATTT FFFFFFFFFFFFFF:FF:FFFFFFFFFFFF,:FFFF:FFFF:,FFF,FFF:FFFFF:FF:,FF:FF,,FFFF,FF,FFF,,FFF,FFF,FFFFFFF,FF,,FFF YT:Z:UP Now starting a Bowtie 2 paired-end alignment for GAread1CTread2GAgenome (reading in sequences from EF06-EM06-Larvae_R1_001.fastp-trim.20220827.fq.gz_G_to_A.fastq and EF06-EM06-Larvae_R2_001.fastp-trim.20220827.fq.gz_C_to_T.fastq, with the options: -q --score-min L,0,-0.4 -p 8 --reorder --ignore-quals --no-mixed --no-discordant --dovetail --maxins 500 --norc)) Found first alignment: GWNJ-1012:512:GW210315000:4:1101:26178:1047_1:N:0:CCAAGTCT+TCATCCTT/1 77 * 0 0 * * 0 0 ANACCATCAATATAACTTTCTAACCATTCAACTTTTCATTATTCATAATTATACATACTTTCCTTTAATTAAACATATAAAAAAAAATTAAATTAATTAAAAAA F#FFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFF:FFFFFFFFFFFFFFFFFF YT:Z:UP GWNJ-1012:512:GW210315000:4:1101:26178:1047_2:N:0:CCAAGTCT+TCATCCTT/2 141 * 0 0 * * 0 0 TTTTTTAATTAATTTAATTTTTTTTTATATGTTTAATTAAAGGAAAGTATGTATAATTATGAATAATGAAAAGTTTAATGGTTATAAAGTTATATTTATTGTTT FFFFFFFFFFFFFF:FF:FFFFFFFFFFFF,:FFFF:FFFF:,FFF,FFF:FFFFF:FF:,FF:FF,,FFFF,FF,FFF,,FFF,FFF,FFFFFFF,FF,,FFF YT:Z:UP Now starting a Bowtie 2 paired-end alignment for GAread1CTread2CTgenome (reading in sequences from EF06-EM06-Larvae_R1_001.fastp-trim.20220827.fq.gz_G_to_A.fastq and EF06-EM06-Larvae_R2_001.fastp-trim.20220827.fq.gz_C_to_T.fastq, with the options: -q --score-min L,0,-0.4 -p 8 --reorder --ignore-quals --no-mixed --no-discordant --dovetail --maxins 500 --nofw)) Found first alignment: GWNJ-1012:512:GW210315000:4:1101:26178:1047_1:N:0:CCAAGTCT+TCATCCTT/1 77 * 0 0 * * 0 0 ANACCATCAATATAACTTTCTAACCATTCAACTTTTCATTATTCATAATTATACATACTTTCCTTTAATTAAACATATAAAAAAAAATTAAATTAATTAAAAAA F#FFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFF:FFFFFFFFFFFFFFFFFF YT:Z:UP GWNJ-1012:512:GW210315000:4:1101:26178:1047_2:N:0:CCAAGTCT+TCATCCTT/2 141 * 0 0 * * 0 0 TTTTTTAATTAATTTAATTTTTTTTTATATGTTTAATTAAAGGAAAGTATGTATAATTATGAATAATGAAAAGTTTAATGGTTATAAAGTTATATTTATTGTTT FFFFFFFFFFFFFF:FF:FFFFFFFFFFFF,:FFFF:FFFF:,FFF,FFF:FFFFF:FF:,FF:FF,,FFFF,FF,FFF,,FFF,FFF,FFFFFFF,FF,,FFF YT:Z:UP Now starting a Bowtie 2 paired-end alignment for CTread1GAread2GAgenome (reading in sequences from EF06-EM06-Larvae_R1_001.fastp-trim.20220827.fq.gz_C_to_T.fastq and EF06-EM06-Larvae_R2_001.fastp-trim.20220827.fq.gz_G_to_A.fastq, with the options: -q --score-min L,0,-0.4 -p 8 --reorder --ignore-quals --no-mixed --no-discordant --dovetail --maxins 500 --nofw)) Found first alignment: GWNJ-1012:512:GW210315000:4:1101:26178:1047_1:N:0:CCAAGTCT+TCATCCTT/1 77 * 0 0 * * 0 0 ANATTATTAATATAATTTTTTAATTATTTAATTTTTTATTATTTATAATTATATATATTTTTTTTTAATTAAATATATAAAAAAAAGTTGGATTAATTAGAAAA F#FFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFF:FFFFFFFFFFFFFFFFFF YT:Z:UP GWNJ-1012:512:GW210315000:4:1101:26178:1047_2:N:0:CCAAGTCT+TCATCCTT/2 141 * 0 0 * * 0 0 TTTTCTAATTAATCCAACTTTTTTTTATATATTTAATTAAAAAAAAATATATATAATTATAAATAATAAAAAATTTAATAATTATAAAATTATATTTATTATTT FFFFFFFFFFFFFF:FF:FFFFFFFFFFFF,:FFFF:FFFF:,FFF,FFF:FFFFF:FF:,FF:FF,,FFFF,FF,FFF,,FFF,FFF,FFFFFFF,FF,,FFF YT:Z:UP >>> Writing bisulfite mapping results to EF06-EM06-Larvae_L0-0.4_pe.bam <<< Reading in the sequence files ../../data/EF06-EM06-Larvae_R1_001.fastp-trim.20220827.fq.gz and ../../data/EF06-EM06-Larvae_R2_001.fastp-trim.20220827.fq.gz 10000 reads; of these: 10000 (100.00%) were paired; of these: 9180 (91.80%) aligned concordantly 0 times 409 (4.09%) aligned concordantly exactly 1 time 411 (4.11%) aligned concordantly >1 times 8.20% overall alignment rate 1000010000 reads; of these: reads; of these: 100001000010000 reads; of these: ( ( 10000 (100.00100.00%%100.00) were paired; of these:) were paired; of these:% ) were paired; of these: 91269168 ( (919891.2691.68 (%%91.98) aligned concordantly 0 times) aligned concordantly 0 times% ) aligned concordantly 0 times 447452 ( (4114.474.52 (%%4.11) aligned concordantly exactly 1 time) aligned concordantly exactly 1 time% ) aligned concordantly exactly 1 time 427380 ( (3914.273.80 (%%3.91) aligned concordantly >1 times) aligned concordantly >1 times% ) aligned concordantly >1 times8.748.32 %%8.02 overall alignment rate overall alignment rate% overall alignment rate Processed 10000 sequences in total Successfully deleted the temporary files EF06-EM06-Larvae_R1_001.fastp-trim.20220827.fq.gz_C_to_T.fastq, EF06-EM06-Larvae_R1_001.fastp-trim.20220827.fq.gz_G_to_A.fastq, EF06-EM06-Larvae_R2_001.fastp-trim.20220827.fq.gz_C_to_T.fastq and EF06-EM06-Larvae_R2_001.fastp-trim.20220827.fq.gz_G_to_A.fastq Final Alignment report ====================== Sequence pairs analysed in total: 10000 Final Cytosine Methylation Report ================================= Total number of C's analysed: 54529 Total methylated C's in CpG context: 1489 Total methylated C's in CHG context: 465 Total methylated C's in CHH context: 1986 Total methylated C's in Unknown context: 44 Total unmethylated C's in CpG context: 5803 Total unmethylated C's in CHG context: 10303 Total unmethylated C's in CHH context: 34483 Total unmethylated C's in Unknown context: 160 C methylated in CpG context: 20.4% C methylated in CHG context: 4.3% C methylated in CHH context: 5.4% C methylated in Unknown context (CN or CHN): 21.6% Bismark completed in 0d 0h 0m 27s ==================== Bismark run complete ====================