Mercurial > repos > bgruening > bismark
diff test-data/summary_short.txt @ 13:f211753166bd draft
planemo upload for repository https://github.com/bgruening/galaxytools/tree/master/tools/bismark commit b9780e368b2e46dc541a846519ccc9593226ee0d
author | bgruening |
---|---|
date | Tue, 30 Jul 2019 06:30:36 -0400 |
parents | |
children | 0b656f8c5637 |
line wrap: on
line diff
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/test-data/summary_short.txt Tue Jul 30 06:30:36 2019 -0400 @@ -0,0 +1,495 @@ +Create a temporary index with the offered files from the user. Utilizing the script: bismark_genome_preparation +Generating index with: 'bismark_genome_preparation --bowtie2 /tmp/tmpVM2AEy' +Writing bisulfite genomes out into a single MFA (multi FastA) file + +Bisulfite Genome Indexer version v0.22.1 (last modified: 14 April 2019) + +Step I - Prepare genome folders - completed + + + +Total number of conversions performed: +C->T: 146875 +G->A: 150504 + +Step II - Genome bisulfite conversions - completed + + +Bismark Genome Preparation - Step III: Launching the Bowtie 2 indexer +Please be aware that this process can - depending on genome size - take several hours! +Settings: + Output files: "BS_CT.*.bt2" + Line rate: 6 (line is 64 bytes) + Lines per side: 1 (side is 64 bytes) + Offset rate: 4 (one in 16) + FTable chars: 10 + Strings: unpacked + Max bucket size: default + Max bucket size, sqrt multiplier: default + Max bucket size, len divisor: 4 + Difference-cover sample period: 1024 + Endianness: little + Actual local endianness: little + Sanity checking: disabled + Assertions: disabled + Random seed: 0 + Sizeofs: void*:8, int:4, long:8, size_t:8 +Input files DNA, FASTA: + genome_mfa.CT_conversion.fa +Building a SMALL index +Reading reference sizes + Time reading reference sizes: 00:00:00 +Calculating joined length +Writing header +Reserving space for joined string +Joining reference sequences + Time to join reference sequences: 00:00:00 +bmax according to bmaxDivN setting: 189039 +Using parameters --bmax 141780 --dcv 1024 + Doing ahead-of-time memory usage test + Passed! Constructing with these parameters: --bmax 141780 --dcv 1024 +Constructing suffix-array element generator +Building DifferenceCoverSample + Building sPrime + Building sPrimeOrder + V-Sorting samples + V-Sorting samples time: 00:00:00 + Allocating rank array + Ranking v-sort output + Ranking v-sort output time: 00:00:00 + Invoking Larsson-Sadakane on ranks + Invoking Larsson-Sadakane on ranks time: 00:00:00 + Sanity-checking and returning +Building samples +Reserving space for 12 sample suffixes +Generating random suffixes +QSorting 12 sample offsets, eliminating duplicates +QSorting sample offsets, eliminating duplicates time: 00:00:00 +Multikey QSorting 12 samples + (Using difference cover) + Multikey QSorting samples time: 00:00:00 +Calculating bucket sizes +Splitting and merging + Splitting and merging time: 00:00:00 +Avg bucket size: 756159 (target: 141779) +Converting suffix-array elements to index image +Allocating ftab, absorbFtab +Entering Ebwt loop +Getting block 1 of 1 + No samples; assembling all-inclusive block + Sorting block of length 756159 for bucket 1 + (Using difference cover) + Sorting block time: 00:00:00 +Returning block of 756160 for bucket 1 +Exited Ebwt loop +fchr[A]: 0 +fchr[C]: 235897 +fchr[G]: 235897 +fchr[T]: 386401 +fchr[$]: 756159 +Exiting Ebwt::buildToDisk() +Returning from initFromVector +Wrote 4446745 bytes to primary EBWT file: BS_CT.1.bt2 +Wrote 189044 bytes to secondary EBWT file: BS_CT.2.bt2 +Re-opening _in1 and _in2 as input streams +Returning from Ebwt constructor +Headers: + len: 756159 + bwtLen: 756160 + sz: 189040 + bwtSz: 189040 + lineRate: 6 + offRate: 4 + offMask: 0xfffffff0 + ftabChars: 10 + eftabLen: 20 + eftabSz: 80 + ftabLen: 1048577 + ftabSz: 4194308 + offsLen: 47260 + offsSz: 189040 + lineSz: 64 + sideSz: 64 + sideBwtSz: 48 + sideBwtLen: 192 + numSides: 3939 + numLines: 3939 + ebwtTotLen: 252096 + ebwtTotSz: 252096 + color: 0 + reverse: 0 +Total time for call to driver() for forward index: 00:00:00 +Reading reference sizes + Time reading reference sizes: 00:00:00 +Calculating joined length +Writing header +Reserving space for joined string +Joining reference sequences + Time to join reference sequences: 00:00:00 + Time to reverse reference sequence: 00:00:00 +bmax according to bmaxDivN setting: 189039 +Using parameters --bmax 141780 --dcv 1024 + Doing ahead-of-time memory usage test + Passed! Constructing with these parameters: --bmax 141780 --dcv 1024 +Constructing suffix-array element generator +Building DifferenceCoverSample + Building sPrime + Building sPrimeOrder + V-Sorting samples + V-Sorting samples time: 00:00:00 + Allocating rank array + Ranking v-sort output + Ranking v-sort output time: 00:00:00 + Invoking Larsson-Sadakane on ranks + Invoking Larsson-Sadakane on ranks time: 00:00:00 + Sanity-checking and returning +Building samples +Reserving space for 12 sample suffixes +Generating random suffixes +QSorting 12 sample offsets, eliminating duplicates +QSorting sample offsets, eliminating duplicates time: 00:00:00 +Multikey QSorting 12 samples + (Using difference cover) + Multikey QSorting samples time: 00:00:00 +Calculating bucket sizes +Splitting and merging + Splitting and merging time: 00:00:00 +Avg bucket size: 756159 (target: 141779) +Converting suffix-array elements to index image +Allocating ftab, absorbFtab +Entering Ebwt loop +Getting block 1 of 1 + No samples; assembling all-inclusive block + Sorting block of length 756159 for bucket 1 + (Using difference cover) + Sorting block time: 00:00:00 +Returning block of 756160 for bucket 1 +Exited Ebwt loop +fchr[A]: 0 +fchr[C]: 235897 +fchr[G]: 235897 +fchr[T]: 386401 +fchr[$]: 756159 +Exiting Ebwt::buildToDisk() +Returning from initFromVector +Wrote 4446745 bytes to primary EBWT file: BS_CT.rev.1.bt2 +Wrote 189044 bytes to secondary EBWT file: BS_CT.rev.2.bt2 +Re-opening _in1 and _in2 as input streams +Returning from Ebwt constructor +Headers: + len: 756159 + bwtLen: 756160 + sz: 189040 + bwtSz: 189040 + lineRate: 6 + offRate: 4 + offMask: 0xfffffff0 + ftabChars: 10 + eftabLen: 20 + eftabSz: 80 + ftabLen: 1048577 + ftabSz: 4194308 + offsLen: 47260 + offsSz: 189040 + lineSz: 64 + sideSz: 64 + sideBwtSz: 48 + sideBwtLen: 192 + numSides: 3939 + numLines: 3939 + ebwtTotLen: 252096 + ebwtTotSz: 252096 + color: 0 + reverse: 1 +Total time for backward call to driver() for mirror index: 00:00:00 +Settings: + Output files: "BS_GA.*.bt2" + Line rate: 6 (line is 64 bytes) + Lines per side: 1 (side is 64 bytes) + Offset rate: 4 (one in 16) + FTable chars: 10 + Strings: unpacked + Max bucket size: default + Max bucket size, sqrt multiplier: default + Max bucket size, len divisor: 4 + Difference-cover sample period: 1024 + Endianness: little + Actual local endianness: little + Sanity checking: disabled + Assertions: disabled + Random seed: 0 + Sizeofs: void*:8, int:4, long:8, size_t:8 +Input files DNA, FASTA: + genome_mfa.GA_conversion.fa +Building a SMALL index +Reading reference sizes + Time reading reference sizes: 00:00:00 +Calculating joined length +Writing header +Reserving space for joined string +Joining reference sequences + Time to join reference sequences: 00:00:00 +bmax according to bmaxDivN setting: 189039 +Using parameters --bmax 141780 --dcv 1024 + Doing ahead-of-time memory usage test + Passed! Constructing with these parameters: --bmax 141780 --dcv 1024 +Constructing suffix-array element generator +Building DifferenceCoverSample + Building sPrime + Building sPrimeOrder + V-Sorting samples + V-Sorting samples time: 00:00:00 + Allocating rank array + Ranking v-sort output + Ranking v-sort output time: 00:00:00 + Invoking Larsson-Sadakane on ranks + Invoking Larsson-Sadakane on ranks time: 00:00:00 + Sanity-checking and returning +Building samples +Reserving space for 12 sample suffixes +Generating random suffixes +QSorting 12 sample offsets, eliminating duplicates +QSorting sample offsets, eliminating duplicates time: 00:00:00 +Multikey QSorting 12 samples + (Using difference cover) + Multikey QSorting samples time: 00:00:00 +Calculating bucket sizes +Splitting and merging + Splitting and merging time: 00:00:00 +Avg bucket size: 756159 (target: 141779) +Converting suffix-array elements to index image +Allocating ftab, absorbFtab +Entering Ebwt loop +Getting block 1 of 1 + No samples; assembling all-inclusive block + Sorting block of length 756159 for bucket 1 + (Using difference cover) + Sorting block time: 00:00:00 +Returning block of 756160 for bucket 1 +Exited Ebwt loop +fchr[A]: 0 +fchr[C]: 386401 +fchr[G]: 533276 +fchr[T]: 533276 +fchr[$]: 756159 +Exiting Ebwt::buildToDisk() +Returning from initFromVector +Wrote 4446745 bytes to primary EBWT file: BS_GA.1.bt2 +Wrote 189044 bytes to secondary EBWT file: BS_GA.2.bt2 +Re-opening _in1 and _in2 as input streams +Returning from Ebwt constructor +Headers: + len: 756159 + bwtLen: 756160 + sz: 189040 + bwtSz: 189040 + lineRate: 6 + offRate: 4 + offMask: 0xfffffff0 + ftabChars: 10 + eftabLen: 20 + eftabSz: 80 + ftabLen: 1048577 + ftabSz: 4194308 + offsLen: 47260 + offsSz: 189040 + lineSz: 64 + sideSz: 64 + sideBwtSz: 48 + sideBwtLen: 192 + numSides: 3939 + numLines: 3939 + ebwtTotLen: 252096 + ebwtTotSz: 252096 + color: 0 + reverse: 0 +Total time for call to driver() for forward index: 00:00:00 +Reading reference sizes + Time reading reference sizes: 00:00:00 +Calculating joined length +Writing header +Reserving space for joined string +Joining reference sequences + Time to join reference sequences: 00:00:00 + Time to reverse reference sequence: 00:00:00 +bmax according to bmaxDivN setting: 189039 +Using parameters --bmax 141780 --dcv 1024 + Doing ahead-of-time memory usage test + Passed! Constructing with these parameters: --bmax 141780 --dcv 1024 +Constructing suffix-array element generator +Building DifferenceCoverSample + Building sPrime + Building sPrimeOrder + V-Sorting samples + V-Sorting samples time: 00:00:00 + Allocating rank array + Ranking v-sort output + Ranking v-sort output time: 00:00:00 + Invoking Larsson-Sadakane on ranks + Invoking Larsson-Sadakane on ranks time: 00:00:00 + Sanity-checking and returning +Building samples +Reserving space for 12 sample suffixes +Generating random suffixes +QSorting 12 sample offsets, eliminating duplicates +QSorting sample offsets, eliminating duplicates time: 00:00:00 +Multikey QSorting 12 samples + (Using difference cover) + Multikey QSorting samples time: 00:00:00 +Calculating bucket sizes +Splitting and merging + Splitting and merging time: 00:00:00 +Avg bucket size: 756159 (target: 141779) +Converting suffix-array elements to index image +Allocating ftab, absorbFtab +Entering Ebwt loop +Getting block 1 of 1 + No samples; assembling all-inclusive block + Sorting block of length 756159 for bucket 1 + (Using difference cover) + Sorting block time: 00:00:00 +Returning block of 756160 for bucket 1 +Exited Ebwt loop +fchr[A]: 0 +fchr[C]: 386401 +fchr[G]: 533276 +fchr[T]: 533276 +fchr[$]: 756159 +Exiting Ebwt::buildToDisk() +Returning from initFromVector +Wrote 4446745 bytes to primary EBWT file: BS_GA.rev.1.bt2 +Wrote 189044 bytes to secondary EBWT file: BS_GA.rev.2.bt2 +Re-opening _in1 and _in2 as input streams +Returning from Ebwt constructor +Headers: + len: 756159 + bwtLen: 756160 + sz: 189040 + bwtSz: 189040 + lineRate: 6 + offRate: 4 + offMask: 0xfffffff0 + ftabChars: 10 + eftabLen: 20 + eftabSz: 80 + ftabLen: 1048577 + ftabSz: 4194308 + offsLen: 47260 + offsSz: 189040 + lineSz: 64 + sideSz: 64 + sideBwtSz: 48 + sideBwtLen: 192 + numSides: 3939 + numLines: 3939 + ebwtTotLen: 252096 + ebwtTotSz: 252096 + color: 0 + reverse: 1 +Total time for backward call to driver() for mirror index: 00:00:01 +Running bismark with: 'bismark --bam --gzip --temp_dir /tmp/tmpHOWuwJ -o /tmp/tmpHOWuwJ/results --quiet --fastq -L 20 -D 15 -R 2 --un --ambiguous /tmp/tmpVM2AEy input_1.fq' +Bowtie 2 seems to be working fine (tested command 'bowtie2 --version' [2.3.5]) +Output format is BAM (default) +Alignments will be written out in BAM format. Samtools found here: '/home/abretaud/miniconda3/envs/mulled-v1-9f2317dbfb405ed6926c55752e5c11678eee3256a6ea680d1c0f912251153030/bin/samtools' +Reference genome folder provided is /tmp/tmpVM2AEy/ (absolute path is '/tmp/tmpVM2AEy/)' +FastQ format specified + +Input files to be analysed (in current folder '/tmp/tmpq6T4hb/job_working_directory/000/8/working'): +input_1.fq +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!) +Created output directory /tmp/tmpHOWuwJ/results/! + +Output will be written into the directory: /tmp/tmpHOWuwJ/results/ + +Using temp directory: /tmp/tmpHOWuwJ +Temporary files will be written into the directory: /tmp/tmpHOWuwJ/ +Setting parallelization to single-threaded (default) + +Summary of all aligner options: -q -L 20 -D 15 -R 2 --score-min L,0,-0.2 --ignore-quals --quiet +Current working directory is: /tmp/tmpq6T4hb/job_working_directory/000/8/working + +Now reading in and storing sequence information of the genome specified in: /tmp/tmpVM2AEy/ + +chr chrY_JH584300_random (182347 bp) +chr chrY_JH584301_random (259875 bp) +chr chrY_JH584302_random (155838 bp) +chr chrY_JH584303_random (158099 bp) + +Single-core mode: setting pid to 1 + +Single-end alignments will be performed +======================================= + +Input file is in FastQ format +Writing a C -> T converted version of the input file input_1.fq to /tmp/tmpHOWuwJ/input_1.fq_C_to_T.fastq.gz + +Created C -> T converted version of the FastQ file input_1.fq (1000 sequences in total) + +Input file is input_1.fq_C_to_T.fastq.gz (FastQ) + +Now running 2 instances of Bowtie 2 against the bisulfite genome of /tmp/tmpVM2AEy/ with the specified options: -q -L 20 -D 15 -R 2 --score-min L,0,-0.2 --ignore-quals --quiet + +Now starting the Bowtie 2 aligner for CTreadCTgenome (reading in sequences from /tmp/tmpHOWuwJ/input_1.fq_C_to_T.fastq.gz with options -q -L 20 -D 15 -R 2 --score-min L,0,-0.2 --ignore-quals --quiet --norc) +Using Bowtie 2 index: /tmp/tmpVM2AEy/Bisulfite_Genome/CT_conversion/BS_CT + +Found first alignment: 1_1 4 * 0 0 * * 0 0 TTGTATATATTAGATAAATTAATTTTTTTTGTTTGTATGTTAAATTTTTTAATTAATTTATTAATATTTTGTGAATTTTTAGATA AAAAAEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEAEEAEEEEEE YT:Z:UU +Now starting the Bowtie 2 aligner for CTreadGAgenome (reading in sequences from /tmp/tmpHOWuwJ/input_1.fq_C_to_T.fastq.gz with options -q -L 20 -D 15 -R 2 --score-min L,0,-0.2 --ignore-quals --quiet --nofw) +Using Bowtie 2 index: /tmp/tmpVM2AEy/Bisulfite_Genome/GA_conversion/BS_GA + +Found first alignment: 1_1 4 * 0 0 * * 0 0 TTGTATATATTAGATAAATTAATTTTTTTTGTTTGTATGTTAAATTTTTTAATTAATTTATTAATATTTTGTGAATTTTTAGATA AAAAAEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEAEEAEEEEEE YT:Z:UU + +>>> Writing bisulfite mapping results to /tmp/tmpHOWuwJ/results/input_1_bismark_bt2.bam <<< + +Unmapped sequences will be written to /tmp/tmpHOWuwJ/results/input_1.fq_unmapped_reads.fq.gz +Ambiguously mapping sequences will be written to /tmp/tmpHOWuwJ/results/input_1.fq_ambiguous_reads.fq.gz + +Reading in the sequence file input_1.fq +Processed 1000 sequences in total + + +Successfully deleted the temporary file /tmp/tmpHOWuwJ/input_1.fq_C_to_T.fastq.gz + +Final Alignment report +====================== +Sequences analysed in total: 1000 +Number of alignments with a unique best hit from the different alignments: 8 +Mapping efficiency: 0.8% + +Sequences with no alignments under any condition: 983 +Sequences did not map uniquely: 9 +Sequences which were discarded because genomic sequence could not be extracted: 0 + +Number of sequences with unique best (first) alignment came from the bowtie output: +CT/CT: 6 ((converted) top strand) +CT/GA: 2 ((converted) bottom strand) +GA/CT: 0 (complementary to (converted) top strand) +GA/GA: 0 (complementary to (converted) bottom strand) + +Number of alignments to (merely theoretical) complementary strands being rejected in total: 0 + +Final Cytosine Methylation Report +================================= +Total number of C's analysed: 143 + +Total methylated C's in CpG context: 3 +Total methylated C's in CHG context: 2 +Total methylated C's in CHH context: 3 +Total methylated C's in Unknown context: 0 + +Total unmethylated C's in CpG context: 1 +Total unmethylated C's in CHG context: 36 +Total unmethylated C's in CHH context: 98 +Total unmethylated C's in Unknown context: 0 + +C methylated in CpG context: 75.0% +C methylated in CHG context: 5.3% +C methylated in CHH context: 3.0% +Can't determine percentage of methylated Cs in Unknown context (CN or CHN) if value was 0 + + +Bismark completed in 0d 0h 0m 5s + +==================== +Bismark run complete +==================== +