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/EF07-EM01-Zygote_R1_001.fastp-trim.20220827.fq.gz ../../data/EF07-EM01-Zygote_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/EF07-EM01-Zygote_score_L0-0.8/ Setting parallelization to single-threaded (default) Summary of all aligner options: -q --score-min L,0,-0.8 -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/EF07-EM01-Zygote_R1_001.fastp-trim.20220827.fq.gz and ../../data/EF07-EM01-Zygote_R2_001.fastp-trim.20220827.fq.gz Input files are in FastQ format Processing reads up to sequence no. 10000 from ../../data/EF07-EM01-Zygote_R1_001.fastp-trim.20220827.fq.gz Writing a C -> T converted version of the input file EF07-EM01-Zygote_R1_001.fastp-trim.20220827.fq.gz to EF07-EM01-Zygote_R1_001.fastp-trim.20220827.fq.gz_C_to_T.fastq Writing a G -> A converted version of the input file EF07-EM01-Zygote_R1_001.fastp-trim.20220827.fq.gz to EF07-EM01-Zygote_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 EF07-EM01-Zygote_R1_001.fastp-trim.20220827.fq.gz (10001 sequences in total) Processing reads up to sequence no. 10000 from ../../data/EF07-EM01-Zygote_R2_001.fastp-trim.20220827.fq.gz Writing a C -> T converted version of the input file EF07-EM01-Zygote_R2_001.fastp-trim.20220827.fq.gz to EF07-EM01-Zygote_R2_001.fastp-trim.20220827.fq.gz_C_to_T.fastq Writing a G -> A converted version of the input file EF07-EM01-Zygote_R2_001.fastp-trim.20220827.fq.gz to EF07-EM01-Zygote_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 EF07-EM01-Zygote_R2_001.fastp-trim.20220827.fq.gz (10001 sequences in total) Input files are EF07-EM01-Zygote_R1_001.fastp-trim.20220827.fq.gz_C_to_T.fastq and EF07-EM01-Zygote_R1_001.fastp-trim.20220827.fq.gz_G_to_A.fastq and EF07-EM01-Zygote_R2_001.fastp-trim.20220827.fq.gz_C_to_T.fastq and EF07-EM01-Zygote_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,-0.8 -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 EF07-EM01-Zygote_R1_001.fastp-trim.20220827.fq.gz_C_to_T.fastq and EF07-EM01-Zygote_R2_001.fastp-trim.20220827.fq.gz_G_to_A.fastq, with the options: -q --score-min L,0,-0.8 -p 8 --reorder --ignore-quals --no-mixed --no-discordant --dovetail --maxins 500 --norc)) Found first alignment: GWNJ-1012:512:GW210315000:4:1101:25870:1047_1:N:0:GTCGGAGC+TTATAACC/1 77 * 0 0 * * 0 0 GNTAAATTTATAAATTTAATTTAAAAATTAAATTTTAATTAAATTATAAATAATATTTAATATAATTTTATAATAAATATAGTTTATAGTT F#FFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFF:FFFFFFFF:FFFFFFFFFFFFF:F:FFFFFFFFFFF YT:Z:UP GWNJ-1012:512:GW210315000:4:1101:25870:1047_2:N:0:GTCGGAGC+TTATAACC/2 141 * 0 0 * * 0 0 AACTATAAACTATATTTATTATAAAATTATATTAAATATTATTTATAATTTAATTAAAATTTAATTTTTAAATTAAATTTATAAATTTATC FFFFFFFFFFFF::FFFFFFFFFFFFFFF:FFFFFF,F:FFF:FFFFFFFF:FFFFFFFFFFF:F:FFFFFFFFFFFFFFFFFF,FF:FFF YT:Z:UP Now starting a Bowtie 2 paired-end alignment for GAread1CTread2GAgenome (reading in sequences from EF07-EM01-Zygote_R1_001.fastp-trim.20220827.fq.gz_G_to_A.fastq and EF07-EM01-Zygote_R2_001.fastp-trim.20220827.fq.gz_C_to_T.fastq, with the options: -q --score-min L,0,-0.8 -p 8 --reorder --ignore-quals --no-mixed --no-discordant --dovetail --maxins 500 --norc)) Found first alignment: GWNJ-1012:512:GW210315000:4:1101:25870:1047_1:N:0:GTCGGAGC+TTATAACC/1 77 * 0 0 * * 0 0 ANCAAACTTATAAATTCAATTTAAAAATCAAATCCTAACTAAACTATAAACAATATTTAACACAACTTTATAATAAACATAATTTATAATT F#FFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFF:FFFFFFFF:FFFFFFFFFFFFF:F:FFFFFFFFFFF YT:Z:UP GWNJ-1012:512:GW210315000:4:1101:25870:1047_2:N:0:GTCGGAGC+TTATAACC/2 141 * 0 0 * * 0 0 AATTATAAATTATGTTTATTATAAAGTTGTGTTAAATATTGTTTATAGTTTAGTTAGGATTTGATTTTTAAATTGAATTTATAAGTTTGTT FFFFFFFFFFFF::FFFFFFFFFFFFFFF:FFFFFF,F:FFF:FFFFFFFF:FFFFFFFFFFF:F:FFFFFFFFFFFFFFFFFF,FF:FFF YT:Z:UP Now starting a Bowtie 2 paired-end alignment for GAread1CTread2CTgenome (reading in sequences from EF07-EM01-Zygote_R1_001.fastp-trim.20220827.fq.gz_G_to_A.fastq and EF07-EM01-Zygote_R2_001.fastp-trim.20220827.fq.gz_C_to_T.fastq, with the options: -q --score-min L,0,-0.8 -p 8 --reorder --ignore-quals --no-mixed --no-discordant --dovetail --maxins 500 --nofw)) Found first alignment: GWNJ-1012:512:GW210315000:4:1101:25870:1047_1:N:0:GTCGGAGC+TTATAACC/1 77 * 0 0 * * 0 0 ANCAAACTTATAAATTCAATTTAAAAATCAAATCCTAACTAAACTATAAACAATATTTAACACAACTTTATAATAAACATAATTTATAATT F#FFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFF:FFFFFFFF:FFFFFFFFFFFFF:F:FFFFFFFFFFF YT:Z:UP GWNJ-1012:512:GW210315000:4:1101:25870:1047_2:N:0:GTCGGAGC+TTATAACC/2 141 * 0 0 * * 0 0 AATTATAAATTATGTTTATTATAAAGTTGTGTTAAATATTGTTTATAGTTTAGTTAGGATTTGATTTTTAAATTGAATTTATAAGTTTGTT FFFFFFFFFFFF::FFFFFFFFFFFFFFF:FFFFFF,F:FFF:FFFFFFFF:FFFFFFFFFFF:F:FFFFFFFFFFFFFFFFFF,FF:FFF YT:Z:UP Now starting a Bowtie 2 paired-end alignment for CTread1GAread2GAgenome (reading in sequences from EF07-EM01-Zygote_R1_001.fastp-trim.20220827.fq.gz_C_to_T.fastq and EF07-EM01-Zygote_R2_001.fastp-trim.20220827.fq.gz_G_to_A.fastq, with the options: -q --score-min L,0,-0.8 -p 8 --reorder --ignore-quals --no-mixed --no-discordant --dovetail --maxins 500 --nofw)) Found first alignment: GWNJ-1012:512:GW210315000:4:1101:25870:1047_1:N:0:GTCGGAGC+TTATAACC/1 77 * 0 0 * * 0 0 GNTAAATTTATAAATTTAATTTAAAAATTAAATTTTAATTAAATTATAAATAATATTTAATATAATTTTATAATAAATATAGTTTATAGTT F#FFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFF:FFFFFFFF:FFFFFFFFFFFFF:F:FFFFFFFFFFF YT:Z:UP GWNJ-1012:512:GW210315000:4:1101:25870:1047_2:N:0:GTCGGAGC+TTATAACC/2 141 * 0 0 * * 0 0 AACTATAAACTATATTTATTATAAAATTATATTAAATATTATTTATAATTTAATTAAAATTTAATTTTTAAATTAAATTTATAAATTTATC FFFFFFFFFFFF::FFFFFFFFFFFFFFF:FFFFFF,F:FFF:FFFFFFFF:FFFFFFFFFFF:F:FFFFFFFFFFFFFFFFFF,FF:FFF YT:Z:UP >>> Writing bisulfite mapping results to EF07-EM01-Zygote_L0-0.8_pe.bam <<< Reading in the sequence files ../../data/EF07-EM01-Zygote_R1_001.fastp-trim.20220827.fq.gz and ../../data/EF07-EM01-Zygote_R2_001.fastp-trim.20220827.fq.gz 10000 reads; of these: 100001000010000 reads; of these: ( reads; of these: 100.00 %1000010000) were paired; of these: ( ( 100.00100.009327%% () were paired; of these:) were paired; of these:93.27 % ) aligned concordantly 0 times91059094 ( ( 91.0590.94285%% () aligned concordantly 0 times) aligned concordantly 0 times2.85 % ) aligned concordantly exactly 1 time372366 ( ( 3.723.66388%% () aligned concordantly exactly 1 time) aligned concordantly exactly 1 time3.88 % ) aligned concordantly >1 times523540 ( (6.735.235.40%%% overall alignment rate) aligned concordantly >1 times) aligned concordantly >1 times 8.959.06%% overall alignment rate overall alignment rate 10000 reads; of these: 10000 (100.00%) were paired; of these: 9372 (93.72%) aligned concordantly 0 times 257 (2.57%) aligned concordantly exactly 1 time 371 (3.71%) aligned concordantly >1 times 6.28% overall alignment rate Processed 10000 sequences in total Successfully deleted the temporary files EF07-EM01-Zygote_R1_001.fastp-trim.20220827.fq.gz_C_to_T.fastq, EF07-EM01-Zygote_R1_001.fastp-trim.20220827.fq.gz_G_to_A.fastq, EF07-EM01-Zygote_R2_001.fastp-trim.20220827.fq.gz_C_to_T.fastq and EF07-EM01-Zygote_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: 33262 Total methylated C's in CpG context: 588 Total methylated C's in CHG context: 131 Total methylated C's in CHH context: 1230 Total methylated C's in Unknown context: 73 Total unmethylated C's in CpG context: 3517 Total unmethylated C's in CHG context: 6083 Total unmethylated C's in CHH context: 21713 Total unmethylated C's in Unknown context: 323 C methylated in CpG context: 14.3% C methylated in CHG context: 2.1% C methylated in CHH context: 5.4% C methylated in Unknown context (CN or CHN): 18.4% Bismark completed in 0d 0h 0m 14s ==================== Bismark run complete ====================