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I tried running the test example command using snakemake. I encountered the error message:
"danbing-tk: src/aQueryFasta_thread.h:457: void readBinaryIndex(kmerIndex_uint32_umap&, std::vector&, std::string&): Assertion `fin' failed."
If you could give me some suggestion about what should I do to make the command successfully, it will be appreciated.
The following is the complete log:
Building DAG of jobs...
Using shell: /bin/bash
Provided cores: 4
Rules claiming more threads will be scaled down.
Job counts:
count jobs
1 GenPanGenomeGraph
2 GenPrunedGenomeGraph
2 GenRawGenomeGraph
1 GenSerializedGraphAndIndex
1 all
7
if [ 1 == "1" ]; then
samtools fasta -@2 -n /public/home/software/danbing-tk-1.3/test/input/HG00733.filtered.reads.bam |
/public/home/software/danbing-tk-1.3//bin/bam2pe -fai /dev/stdin |
/public/home/software/danbing-tk-1.3//bin/danbing-tk -g 50 -k 21 -qs /public/home/software/danbing-tk-1.3/test/output//HG00733.rawPB -fai /dev/stdin -o HG00733.rawIL -p 24 -cth 45 -rth 0.5
fi
Using orthology map, total number of loci: Using orthology map, total number of loci: 11
building and counting building and counting /public/home/software/danbing-tk-1.3/test/output/HG00514.0.tr.fasta/public/home/software/danbing-tk-1.3/test/output/HG00733.0.tr.fasta kmers
kmers
building and counting /public/home/software/danbing-tk-1.3/test/output/HG00733.1.tr.fasta kmers
writing outputs
building and counting /public/home/software/danbing-tk-1.3/test/output/HG00514.1.tr.fasta kmers
writing outputs
fname: /dev/stdin
fname: /dev/stdin
use baitDB: 0
extract fasta: 0
interleaved: 1
sim mode: 0
trim mode: 0
augmentation mode: 0
graph threading mode: 1
output alignment: 0
use baitDB: 0
extract fasta: 0
interleaved: 1output successfully aligned reads only:
0sim mode:
0k:
21trim mode:
0# of subsampled kmers in pre-filtering:
4augmentation mode:
0minimal # of matches in pre-filtering:
1graph threading mode:
1Cthreshold:
45output alignment:
0Rthreshold:
0.5output successfully aligned reads only:
0threading Cthreshold:
50k:
21Running both step1 (kmer-based filtering) and step2 (threading)
of subsampled kmers in pre-filtering: fastx: 4/dev/stdin
minimal # of matches in pre-filtering: query: 1/public/home/software/danbing-tk-1.3/test/output//HG00514.rawPB
.(tr/ntr).kmersCthreshold:
45
total number of loci in Rthreshold: /public/home/software/danbing-tk-1.3/test/output//HG00514.rawPB.tr.kmers: 0.5
threading Cthreshold: 50
Running both step1 (kmer-based filtering) and step2 (threading)
fastx: /dev/stdin
query: /public/home/software/danbing-tk-1.3/test/output//HG00733.rawPB.(tr/ntr).kmers
if [ 1 == "1" ]; then
samtools fasta -@2 -n /public/home/software/danbing-tk-1.3/test/input/HG00733.filtered.reads.bam |
/public/home/software/danbing-tk-1.3//bin/bam2pe -fai /dev/stdin |
/public/home/software/danbing-tk-1.3//bin/danbing-tk -g 50 -k 21 -qs /public/home/software/danbing-tk-1.3/test/output//HG00733.rawPB -fai /dev/stdin -o HG00733.rawIL -p 24 -cth 45 -rth 0.5
fi
(one of the commands exited with non-zero exit code; note that snakemake uses bash strict mode!)
Removing output files of failed job GenRawGenomeGraph since they might be corrupted:
/public/home/software/danbing-tk-1.3/test/output/HG00514.rawPB.tr.kmers, /public/home/software/danbing-tk-1.3/test/output/HG00514.rawPB.ntr.kmers, /public/home/software/danbing-tk-1.3/test/output/HG00514.rawPB.graph.kmers, /public/home/software/danbing-tk-1.3/test/output/HG00514.rawIL.tr.kmers
Removing output files of failed job GenRawGenomeGraph since they might be corrupted:
/public/home/software/danbing-tk-1.3/test/output/HG00733.rawPB.tr.kmers, /public/home/software/danbing-tk-1.3/test/output/HG00733.rawPB.ntr.kmers, /public/home/software/danbing-tk-1.3/test/output/HG00733.rawPB.graph.kmers, /public/home/software/danbing-tk-1.3/test/output/HG00733.rawIL.tr.kmers
Shutting down, this might take some time.
Exiting because a job execution failed. Look above for error message
Best wishes,
Huiying
The text was updated successfully, but these errors were encountered:
Dear ChaissonLab,
I tried running the test example command using snakemake. I encountered the error message:
"danbing-tk: src/aQueryFasta_thread.h:457: void readBinaryIndex(kmerIndex_uint32_umap&, std::vector&, std::string&): Assertion `fin' failed."
If you could give me some suggestion about what should I do to make the command successfully, it will be appreciated.
The following is the complete log:
Building DAG of jobs...
Using shell: /bin/bash
Provided cores: 4
Rules claiming more threads will be scaled down.
Job counts:
count jobs
1 GenPanGenomeGraph
2 GenPrunedGenomeGraph
2 GenRawGenomeGraph
1 GenSerializedGraphAndIndex
1 all
7
[Mon Feb 14 23:45:53 2022]
rule GenRawGenomeGraph:
input: /public/home/software/danbing-tk-1.3/test/output/HG00514.0.tr.fasta, /public/home/software/danbing-tk-1.3/test/output/HG00514.1.tr.fasta, /public/home/software/danbing-tk-1.3/test/input/HG00514.filtered.reads.bam, /public/home/software/danbing-tk-1.3/test/output/OrthoMap.v2.tsv
output: /public/home/software/danbing-tk-1.3/test/output/HG00514.rawPB.tr.kmers, /public/home/software/danbing-tk-1.3/test/output/HG00514.rawPB.ntr.kmers, /public/home/software/danbing-tk-1.3/test/output/HG00514.rawPB.graph.kmers, /public/home/software/danbing-tk-1.3/test/output/HG00514.rawIL.tr.kmers
jobid: 13
wildcards: genome=HG00514
priority: 95
resources: cores=24, mem=25
set -eu
ulimit -c 20000
cd /public/home/software/danbing-tk-1.3/test/output/
module load gcc
/public/home/software/danbing-tk-1.3//bin/vntr2kmers_thread -g -m <(cut -f$((0+1)),$ ((0+2)) /public/home/software/danbing-tk-1.3/test/output/OrthoMap.v2.tsv) -k 21 -fs 700 -ntr 700 -o HG00514.rawPB -fa 2 /public/home/software/danbing-tk-1.3/test/output/HG00514.0.tr.fasta /public/home/software/danbing-tk-1.3/test/output/HG00514.1.tr.fasta
if [ 1 == "1" ]; then
samtools fasta -@2 -n /public/home/software/danbing-tk-1.3/test/input/HG00514.filtered.reads.bam |
/public/home/software/danbing-tk-1.3//bin/bam2pe -fai /dev/stdin |
/public/home/software/danbing-tk-1.3//bin/danbing-tk -g 50 -k 21 -qs /public/home/software/danbing-tk-1.3/test/output//HG00514.rawPB -fai /dev/stdin -o HG00514.rawIL -p 24 -cth 45 -rth 0.5
fi
rule GenRawGenomeGraph:
input: /public/home/software/danbing-tk-1.3/test/output/HG00733.0.tr.fasta, /public/home/software/danbing-tk-1.3/test/output/HG00733.1.tr.fasta, /public/home/software/danbing-tk-1.3/test/input/HG00733.filtered.reads.bam, /public/home/software/danbing-tk-1.3/test/output/OrthoMap.v2.tsv
output: /public/home/software/danbing-tk-1.3/test/output/HG00733.rawPB.tr.kmers, /public/home/software/danbing-tk-1.3/test/output/HG00733.rawPB.ntr.kmers, /public/home/software/danbing-tk-1.3/test/output/HG00733.rawPB.graph.kmers, /public/home/software/danbing-tk-1.3/test/output/HG00733.rawIL.tr.kmers
jobid: 14
wildcards: genome=HG00733
priority: 95
resources: cores=24, mem=25
set -eu
ulimit -c 20000
cd /public/home/software/danbing-tk-1.3/test/output/
module load gcc
/public/home/software/danbing-tk-1.3//bin/vntr2kmers_thread -g -m <(cut -f$((2+1)),$ ((2+2)) /public/home/software/danbing-tk-1.3/test/output/OrthoMap.v2.tsv) -k 21 -fs 700 -ntr 700 -o HG00733.rawPB -fa 2 /public/home/software/danbing-tk-1.3/test/output/HG00733.0.tr.fasta /public/home/software/danbing-tk-1.3/test/output/HG00733.1.tr.fasta
if [ 1 == "1" ]; then
samtools fasta -@2 -n /public/home/software/danbing-tk-1.3/test/input/HG00733.filtered.reads.bam |
/public/home/software/danbing-tk-1.3//bin/bam2pe -fai /dev/stdin |
/public/home/software/danbing-tk-1.3//bin/danbing-tk -g 50 -k 21 -qs /public/home/software/danbing-tk-1.3/test/output//HG00733.rawPB -fai /dev/stdin -o HG00733.rawIL -p 24 -cth 45 -rth 0.5
fi
Using orthology map, total number of loci: Using orthology map, total number of loci: 11
building and counting building and counting /public/home/software/danbing-tk-1.3/test/output/HG00514.0.tr.fasta/public/home/software/danbing-tk-1.3/test/output/HG00733.0.tr.fasta kmers
kmers
building and counting /public/home/software/danbing-tk-1.3/test/output/HG00733.1.tr.fasta kmers
writing outputs
building and counting /public/home/software/danbing-tk-1.3/test/output/HG00514.1.tr.fasta kmers
writing outputs
fname: /dev/stdin
fname: /dev/stdin
use baitDB: 0
extract fasta: 0
interleaved: 1
sim mode: 0
trim mode: 0
augmentation mode: 0
graph threading mode: 1
output alignment: 0
use baitDB: 0
extract fasta: 0
interleaved: 1output successfully aligned reads only:
0sim mode:
0k:
21trim mode:
0# of subsampled kmers in pre-filtering:
4augmentation mode:
0minimal # of matches in pre-filtering:
1graph threading mode:
1Cthreshold:
45output alignment:
0Rthreshold:
0.5output successfully aligned reads only:
0threading Cthreshold:
50k:
21Running both step1 (kmer-based filtering) and step2 (threading)
of subsampled kmers in pre-filtering: fastx: 4/dev/stdin
minimal # of matches in pre-filtering: query: 1/public/home/software/danbing-tk-1.3/test/output//HG00514.rawPB
.(tr/ntr).kmersCthreshold:
45
total number of loci in Rthreshold: /public/home/software/danbing-tk-1.3/test/output//HG00514.rawPB.tr.kmers: 0.5
threading Cthreshold: 50
Running both step1 (kmer-based filtering) and step2 (threading)
fastx: /dev/stdin
query: /public/home/software/danbing-tk-1.3/test/output//HG00733.rawPB.(tr/ntr).kmers
total number of loci in /public/home/software/danbing-tk-1.3/test/output//HG00733.rawPB.tr.kmers: 0
0
deserializing kmerDBi.umap
deserializing kmerDBi.umap
danbing-tk: src/aQueryFasta_thread.h:457: void readBinaryIndex(kmerIndex_uint32_umap&, std::vector&, std::string&): Assertion
fin' failed. danbing-tk: src/aQueryFasta_thread.h:457: void readBinaryIndex(kmerIndex_uint32_umap&, std::vector<unsigned int>&, std::string&): Assertion
fin' failed./bin/bash: line 11: 220388 Broken pipe samtools fasta -@2 -n /public/home/software/danbing-tk-1.3/test/input/HG00514.filtered.reads.bam
220389 | /public/home/zhaoFL/software/danbing-tk-1.3//bin/bam2pe -fai /dev/stdin
220390 Aborted (core dumped) | /public/home/software/danbing-tk-1.3//bin/danbing-tk -g 50 -k 21 -qs /public/home/software/danbing-tk-1.3/test/output//HG00514.rawPB -fai /dev/stdin -o HG00514.rawIL -p 24 -cth 45 -rth 0.5
/bin/bash: line 11: 220385 Broken pipe samtools fasta -@2 -n /public/home/software/danbing-tk-1.3/test/input/HG00733.filtered.reads.bam
220386 | /public/home/software/danbing-tk-1.3//bin/bam2pe -fai /dev/stdin
220387 Aborted (core dumped) | /public/home/software/danbing-tk-1.3//bin/danbing-tk -g 50 -k 21 -qs /public/home/software/danbing-tk-1.3/test/output//HG00733.rawPB -fai /dev/stdin -o HG00733.rawIL -p 24 -cth 45 -rth 0.5
[Mon Feb 14 23:45:54 2022]
Error in rule GenRawGenomeGraph:
[Mon Feb 14 23:45:54 2022]
jobid: 13
Error in rule GenRawGenomeGraph:
output: /public/home/software/danbing-tk-1.3/test/output/HG00514.rawPB.tr.kmers, /public/home/software/danbing-tk-1.3/test/output/HG00514.rawPB.ntr.kmers, /public/home/software/danbing-tk-1.3/test/output/HG00514.rawPB.graph.kmers, /public/home/software/danbing-tk-1.3/test/output/HG00514.rawIL.tr.kmers
jobid: 14
shell:
set -eu
ulimit -c 20000
cd /public/home/software/danbing-tk-1.3/test/output/
module load gcc
/public/home/software/danbing-tk-1.3//bin/vntr2kmers_thread -g -m <(cut -f$((0+1)),$ ((0+2)) /public/home/software/danbing-tk-1.3/test/output/OrthoMap.v2.tsv) -k 21 -fs 700 -ntr 700 -o HG00514.rawPB -fa 2 /public/home/software/danbing-tk-1.3/test/output/HG00514.0.tr.fasta /public/home/software/danbing-tk-1.3/test/output/HG00514.1.tr.fasta
if [ 1 == "1" ]; then
samtools fasta -@2 -n /public/home/software/danbing-tk-1.3/test/input/HG00514.filtered.reads.bam |
/public/home/software/danbing-tk-1.3//bin/bam2pe -fai /dev/stdin |
/public/home/software/danbing-tk-1.3//bin/danbing-tk -g 50 -k 21 -qs /public/home/software/danbing-tk-1.3/test/output//HG00514.rawPB -fai /dev/stdin -o HG00514.rawIL -p 24 -cth 45 -rth 0.5
fi
set -eu
ulimit -c 20000
cd /public/home/software/danbing-tk-1.3/test/output/
module load gcc
/public/home/software/danbing-tk-1.3//bin/vntr2kmers_thread -g -m <(cut -f$((2+1)),$ ((2+2)) /public/home/software/danbing-tk-1.3/test/output/OrthoMap.v2.tsv) -k 21 -fs 700 -ntr 700 -o HG00733.rawPB -fa 2 /public/home/software/danbing-tk-1.3/test/output/HG00733.0.tr.fasta /public/home/software/danbing-tk-1.3/test/output/HG00733.1.tr.fasta
if [ 1 == "1" ]; then
samtools fasta -@2 -n /public/home/software/danbing-tk-1.3/test/input/HG00733.filtered.reads.bam |
/public/home/software/danbing-tk-1.3//bin/bam2pe -fai /dev/stdin |
/public/home/software/danbing-tk-1.3//bin/danbing-tk -g 50 -k 21 -qs /public/home/software/danbing-tk-1.3/test/output//HG00733.rawPB -fai /dev/stdin -o HG00733.rawIL -p 24 -cth 45 -rth 0.5
fi
Removing output files of failed job GenRawGenomeGraph since they might be corrupted:
/public/home/software/danbing-tk-1.3/test/output/HG00514.rawPB.tr.kmers, /public/home/software/danbing-tk-1.3/test/output/HG00514.rawPB.ntr.kmers, /public/home/software/danbing-tk-1.3/test/output/HG00514.rawPB.graph.kmers, /public/home/software/danbing-tk-1.3/test/output/HG00514.rawIL.tr.kmers
Removing output files of failed job GenRawGenomeGraph since they might be corrupted:
/public/home/software/danbing-tk-1.3/test/output/HG00733.rawPB.tr.kmers, /public/home/software/danbing-tk-1.3/test/output/HG00733.rawPB.ntr.kmers, /public/home/software/danbing-tk-1.3/test/output/HG00733.rawPB.graph.kmers, /public/home/software/danbing-tk-1.3/test/output/HG00733.rawIL.tr.kmers
Shutting down, this might take some time.
Exiting because a job execution failed. Look above for error message
Best wishes,
Huiying
The text was updated successfully, but these errors were encountered: