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I am analyzing a single sample (fastq.gz file size ~140 GBytes) leaving the variant caller to the default (medaka).
It stops with an error: "Failed to run medaka consensus" (see below).
No idea where this error comes from. pepper-margin-deepvariant works, instead.
Command used and terminal output
nextflow run nf-core/nanoseq -r 3.1.0 -profile docker -params-file nf-params.json -c custom_paramswhere **nf-params.json**:{ "protocol": "DNA", "outdir": ".\/results", "call_variants": true, "input": "samplesheet.csv", "skip_demultiplexing": true, "call_variants": true, "skip_quantification": true, "skip_fusion_analysis": true, "skip_modification_analysis": true, "max_time": "20.h"}-----OUTPUT:ERROR ~ Error executing process > 'NFCORE_NANOSEQ:NANOSEQ:SHORT_VARIANT_CALLING:MEDAKA_VARIANT (sample_R1)'Caused by: Process `NFCORE_NANOSEQ:NANOSEQ:SHORT_VARIANT_CALLING:MEDAKA_VARIANT (sample_R1)` terminated with an error exit status (1)Command executed: medaka_variant \ -d \ -f genome.fa \ -i sample_R1.sorted.bam \ -o sample_R1 \ -t 12 \ \ cat <<-END_VERSIONS > versions.yml "NFCORE_NANOSEQ:NANOSEQ:SHORT_VARIANT_CALLING:MEDAKA_VARIANT": medaka: $( medaka --version 2>&1 | sed 's/medaka //g' ) END_VERSIONSCommand exit status: 1Command output: ++ Preparing data - Checking program versions Program Version Required Pass bcftools 1.12 1.11 True bgzip 1.12 1.11 True minimap2 2.22 2.11 True samtools 1.12 1.11 True tabix 1.12 1.11 True ++ Running first pass to haplotag reads. + Running consensus calling - Running medaka consensus with /data/runs/2024-06-07/GM23-14050/20240607_1642_1B_PAW01711_387c256b/bfx/work/92/cdf710fd37f3ddd905a51d057c3e2d/sample_R1.sorted.bam --model r941_prom_hac_snp_g507 * Failed to run medaka consensus.Command error: [15:37:15 - Feature] Processed chr11:108891000.0-109890999.0 (median depth 44.0) [15:37:15 - Sampler] Took 0.95s to make features. [15:37:15 - Sampler] Initializing sampler for consensus of region chr11:110889000-111889000. [15:37:16 - Feature] Processed chr11:109890000.0-110889999.0 (median depth 43.0) [15:37:16 - Sampler] Took 0.95s to make features. [15:37:16 - Sampler] Initializing sampler for consensus of region chr11:111888000-112888000. [15:37:16 - Feature] Processed chr11:110889000.0-111888999.0 (median depth 42.0) [15:37:16 - Sampler] Took 0.96s to make features. [15:37:16 - Sampler] Initializing sampler for consensus of region chr11:112887000-113887000. [15:37:17 - Feature] Processed chr11:111888000.0-112887999.1 (median depth 44.0) [15:37:17 - Sampler] Took 0.96s to make features. [15:37:17 - Sampler] Initializing sampler for consensus of region chr11:113886000-114886000. [15:37:17 - Feature] Processed chr11:112887000.0-113886999.0 (median depth 42.0) [15:37:17 - Sampler] Took 0.97s to make features. [15:37:17 - Sampler] Initializing sampler for consensus of region chr11:114885000-115885000. [15:37:17 - PWorker] Batches in cache: 2333. [15:37:17 - PWorker] 4.5% Done (140.0/3103.0 Mbases) in 1721.7s [15:37:20 - Feature] Processed chr11:113886000.0-114885999.0 (median depth 43.0) [15:37:20 - Sampler] Took 3.81s to make features. [15:37:21 - Feature] Processed chr11:114885000.0-115884999.0 (median depth 43.0) [15:37:21 - Sampler] Took 3.96s to make features. [15:37:21 - Sampler] Initializing sampler for consensus of region chr11:115884000-116884000. [15:37:21 - Sampler] Initializing sampler for consensus of region chr11:116883000-117883000. [15:37:22 - Feature] Processed chr11:116883000.0-117882999.3 (median depth 41.0) [15:37:22 - Sampler] Took 1.14s to make features. [15:37:22 - Sampler] Initializing sampler for consensus of region chr11:117882000-118882000. [15:37:22 - Feature] Processed chr11:115884000.0-116883999.0 (median depth 43.0) [15:37:22 - Sampler] Took 1.22s to make features. [15:37:22 - Sampler] Initializing sampler for consensus of region chr11:118881000-119881000. [15:37:23 - Feature] Processed chr11:117882000.0-118881999.0 (median depth 41.0) [15:37:23 - Sampler] Took 1.03s to make features. [15:37:23 - Feature] Processed chr11:118881000.0-119880999.0 (median depth 40.0) [15:37:23 - Sampler] Initializing sampler for consensus of region chr11:119880000-120880000. [15:37:23 - Sampler] Took 0.96s to make features. [15:37:23 - Sampler] Initializing sampler for consensus of region chr11:120879000-121879000. [15:37:24 - Feature] Processed chr11:120879000.0-121878999.0 (median depth 43.0) [15:37:24 - Sampler] Took 0.97s to make features. [15:37:24 - Sampler] Initializing sampler for consensus of region chr11:121878000-122878000. [15:37:24 - Feature] Processed chr11:119880000.0-120879999.0 (median depth 43.0) [15:37:24 - Sampler] Took 1.01s to make features. [15:37:24 - Sampler] Initializing sampler for consensus of region chr11:122877000-123877000. [15:37:25 - Feature] Processed chr11:121878000.0-122877999.0 (median depth 43.0) [15:37:25 - Sampler] Took 1.21s to make features. [15:37:25 - Sampler] Initializing sampler for consensus of region chr11:123876000-124876000. [15:37:25 - Feature] Processed chr11:122877000.0-123876999.0 (median depth 41.0) [15:37:25 - Sampler] Took 1.23s to make features. [15:37:25 - Sampler] Initializing sampler for consensus of region chr11:124875000-125875000. [15:37:26 - PWorker] Batches in cache: 2346. /usr/local/bin/medaka_variant: line 136: 749 Killed medaka consensus "${BAM}" "${PROBS}" --model "${MEDAKAMODEL}" --batch_size "${BATCH_SIZE}" ${REG_OPT} --threads "${THREADS}" ${EXTRAOPTS} * Failed to run medaka consensus.
Description of the bug
I am analyzing a single sample (fastq.gz file size ~140 GBytes) leaving the variant caller to the default (medaka).
It stops with an error: "Failed to run medaka consensus" (see below).
No idea where this error comes from.
pepper-margin-deepvariant
works, instead.Command used and terminal output
Relevant files
No response
System information
NF ver: 24.04.4.5917
Hardware: HPC
Executor: local
Container: Docker
OS: Ubuntu
nf-core/nanoseq ver: 3.1.0
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