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/ (absolute path is '/mmfs1/gscratch/srlab/sr320/github/timeseries_molecular/E-Peve/data/)' 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 10 threads. Please monitor performance closely and tune down if necessary! Input files to be analysed (in current folder '/mmfs1/gscratch/srlab/sr320/github/timeseries_molecular/E-Peve/output/04-Peve-bismark-array'): ../../data/03-Peve-bismark/POR-236-TP1_R1_001.fastp-trim.fq.gz ../../data/03-Peve-bismark/POR-236-TP1_R2_001.fastp-trim.fq.gz Library is assumed to be strand-specific (directional), alignments to strands complementary to the original top or bottom strands will be ignored (i.e. not performed!) Output will be written into the directory: /mmfs1/gscratch/srlab/sr320/github/timeseries_molecular/E-Peve/output/04-Peve-bismark-array/ Setting parallelization to single-threaded (default) Summary of all aligner options: -q --score-min L,0,-0.6 -p 10 --reorder --ignore-quals --no-mixed --no-discordant --dovetail --maxins 500 Current working directory is: /mmfs1/gscratch/srlab/sr320/github/timeseries_molecular/E-Peve/output/04-Peve-bismark-array Now reading in and storing sequence information of the genome specified in: /mmfs1/gscratch/srlab/sr320/github/timeseries_molecular/E-Peve/data/ Single-core mode: setting pid to 1 Paired-end alignments will be performed ======================================= The provided filenames for paired-end alignments are ../../data/03-Peve-bismark/POR-236-TP1_R1_001.fastp-trim.fq.gz and ../../data/03-Peve-bismark/POR-236-TP1_R2_001.fastp-trim.fq.gz Input files are in FastQ format Processing reads up to sequence no. 10000 from ../../data/03-Peve-bismark/POR-236-TP1_R1_001.fastp-trim.fq.gz Writing a C -> T converted version of the input file POR-236-TP1_R1_001.fastp-trim.fq.gz to POR-236-TP1_R1_001.fastp-trim.fq.gz_C_to_T.fastq Created C -> T converted version of the FastQ file POR-236-TP1_R1_001.fastp-trim.fq.gz (10001 sequences in total) Processing reads up to sequence no. 10000 from ../../data/03-Peve-bismark/POR-236-TP1_R2_001.fastp-trim.fq.gz Writing a G -> A converted version of the input file POR-236-TP1_R2_001.fastp-trim.fq.gz to POR-236-TP1_R2_001.fastp-trim.fq.gz_G_to_A.fastq Created G -> A converted version of the FastQ file POR-236-TP1_R2_001.fastp-trim.fq.gz (10001 sequences in total) Input files are POR-236-TP1_R1_001.fastp-trim.fq.gz_C_to_T.fastq and POR-236-TP1_R2_001.fastp-trim.fq.gz_G_to_A.fastq (FastQ) Now running 2 instances of Bowtie 2 against the bisulfite genome of /mmfs1/gscratch/srlab/sr320/github/timeseries_molecular/E-Peve/data/ with the specified options: -q --score-min L,0,-0.6 -p 10 --reorder --ignore-quals --no-mixed --no-discordant --dovetail --maxins 500 Now starting a Bowtie 2 paired-end alignment for CTread1GAread2CTgenome (reading in sequences from POR-236-TP1_R1_001.fastp-trim.fq.gz_C_to_T.fastq and POR-236-TP1_R2_001.fastp-trim.fq.gz_G_to_A.fastq, with the options: -q --score-min L,0,-0.6 -p 10 --reorder --ignore-quals --no-mixed --no-discordant --dovetail --maxins 500 --norc)) Found first alignment: LH00526:197:22KFKVLT4:3:1101:43395:1070_1:N:0:GATCTTGC+TGCTCATG/1 99 Porites_evermani_scaffold_2660_CT_converted 7975 8 121M2D1M5D13M = 8097 251 ATTAATTTTTTTAAAAAAAAAGAAAATGGTTAATTTTGGAGTTTTTTGAGAGTTTATAAGTTATTATGATTAGTTGTTATGTGTTTATTTTTTTTTTAATTTAGTTGTTTGTATAAGAATAGTTTTTGAGTAAAT III9IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII9II9III-I9IIIIIIIII9IIIIIIIIIIIIIII9I-IIIIII9IIIII-I9IIIIIIIIIIIIIIIIIII9 AS:i:-61 XN:i:0 XM:i:5 XO:i:2 XG:i:7 NM:i:12 MD:Z:30A28A15T4A5T34^AT1^TTTAA13 YS:i:-29 YT:Z:CP LH00526:197:22KFKVLT4:3:1101:43395:1070_2:N:0:GATCTTGC+TGCTCATG/2 147 Porites_evermani_scaffold_2660_CT_converted 8097 8 7M6I122M = 7975 -251 TGTATAAGAATAGTTTTTGAGTAAATATGTTTTTAGTGGGGAAAGTTAATTGTGGATTGTGGGTAAGTGTTATAGGTTTATATATTTTAGATGGATTTGATATTAGTATAGTGTTTAGAGGTTTTATTTGTTTGG IIIIIIIIIIIIIIIIII9IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII AS:i:-29 XN:i:0 XM:i:1 XO:i:1 XG:i:6 NM:i:7 MD:Z:3T125 YS:i:-61 YT:Z:CP Now starting a Bowtie 2 paired-end alignment for CTread1GAread2GAgenome (reading in sequences from POR-236-TP1_R1_001.fastp-trim.fq.gz_C_to_T.fastq and POR-236-TP1_R2_001.fastp-trim.fq.gz_G_to_A.fastq, with the options: -q --score-min L,0,-0.6 -p 10 --reorder --ignore-quals --no-mixed --no-discordant --dovetail --maxins 500 --nofw)) Found first alignment: LH00526:197:22KFKVLT4:3:1101:43395:1070_1:N:0:GATCTTGC+TGCTCATG/1 77 * 0 0 * * 0 0 ATTAATTTTTTTAAAAAAAAAGAAAATGGTTAATTTTGGAGTTTTTTGAGAGTTTATAAGTTATTATGATTAGTTGTTATGTGTTTATTTTTTTTTTAATTTAGTTGTTTGTATAAGAATAGTTTTTGAGTAAAT III9IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII9II9III-I9IIIIIIIII9IIIIIIIIIIIIIII9I-IIIIII9IIIII-I9IIIIIIIIIIIIIIIIIII9 YT:Z:UP LH00526:197:22KFKVLT4:3:1101:43395:1070_2:N:0:GATCTTGC+TGCTCATG/2 141 * 0 0 * * 0 0 CCAAACAAATAAAACCTCTAAACACTATACTAATATCAAATCCATCTAAAATATATAAACCTATAACACTTACCCACAATCCACAATTAACTTTCCCCACTAAAAACATATTTACTCAAAAACTATTCTTATACA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII9IIIIIIIIIIIIIIIIII YT:Z:UP >>> Writing bisulfite mapping results to POR-236-TP1_pe.bam <<< Reading in the sequence files ../../data/03-Peve-bismark/POR-236-TP1_R1_001.fastp-trim.fq.gz and ../../data/03-Peve-bismark/POR-236-TP1_R2_001.fastp-trim.fq.gz 10000 reads; of these: 10000 (100.00%) were paired; of these: 5445 (54.45%) aligned concordantly 0 times 2667 (26.67%) aligned concordantly exactly 1 time 1888 (18.88%) aligned concordantly >1 times 45.55% overall alignment rate 10000 reads; of these: 10000 (100.00%) were paired; of these: 5650 (56.50%) aligned concordantly 0 times 2510 (25.10%) aligned concordantly exactly 1 time 1840 (18.40%) aligned concordantly >1 times 43.50% overall alignment rate Chromosomal sequence could not be extracted for LH00526:197:22KFKVLT4:3:1101:43759:15400_1:N:0:GATCTTGC+TGCTCATG Porites_evermani_scaffold_5548 12209 Processed 10000 sequences in total Successfully deleted the temporary files POR-236-TP1_R1_001.fastp-trim.fq.gz_C_to_T.fastq and POR-236-TP1_R2_001.fastp-trim.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: 309821 Total methylated C's in CpG context: 4218 Total methylated C's in CHG context: 396 Total methylated C's in CHH context: 1538 Total methylated C's in Unknown context: 7 Total unmethylated C's in CpG context: 45397 Total unmethylated C's in CHG context: 54240 Total unmethylated C's in CHH context: 204032 Total unmethylated C's in Unknown context: 396 C methylated in CpG context: 8.5% C methylated in CHG context: 0.7% C methylated in CHH context: 0.7% C methylated in Unknown context (CN or CHN): 1.7% Bismark completed in 0d 0h 0m 16s ==================== Bismark run complete ====================