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Hello, I've used SPAdes to assemble my metagenomic datasets however two of my samples are getting stuck in the exact same place repeatedly. I was able to assemble all my samples using megahit without any issues but much prefer SPAdes.
18_R1.filtered_human.fq.gz -2 /home/ctmr/projects/Aron/SPAdes/input/PA18_R2.filtered_human.fq.gz --meta -t 16
System information:
SPAdes version: 3.13.1
Python version: 3.6.7
OS: Linux-3.10.0-862.14.4.el7.x86_64-x86_64-with-redhat-7.6-Nitrogen
Output dir: /home/ctmr/projects/Aron/SPAdes/output/PA18
Mode: read error correction and assembling
Debug mode is turned OFF
Dataset parameters:
Metagenomic mode
Reads:
Library number: 1, library type: paired-end
orientation: fr
left reads: ['/home/ctmr/projects/Aron/SPAdes/input/PA18_R1.filtered_human.fq.gz']
right reads: ['/home/ctmr/projects/Aron/SPAdes/input/PA18_R2.filtered_human.fq.gz']
interlaced reads: not specified
single reads: not specified
merged reads: not specified
Read error correction parameters:
Iterations: 1
PHRED offset will be auto-detected
Corrected reads will be compressed
Assembly parameters:
k: [21, 33, 55]
Repeat resolution is enabled
Mismatch careful mode is turned OFF
MismatchCorrector will be SKIPPED
Coverage cutoff is turned OFF
Other parameters:
Dir for temp files: /home/ctmr/projects/Aron/SPAdes/output/PA18/tmp
Threads: 16
Memory limit (in Gb): 250
======= SPAdes pipeline started. Log can be found here: /home/ctmr/projects/Aron/SPAdes/output/PA18/spades.log
===== Read error correction started.
== Running read error correction tool: /home/ctmr/projects/Aron/SPAdes/.snakemake/conda/edf7c82d/bin/spades-hammer /home/ctmr/projects/Aron/SPAdes/output/PA18/corrected/configs/config.info
0:00:00.000 4M / 4M INFO General (main.cpp : 75) Starting BayesHammer, built from N/A, git revision N/A
0:00:00.000 4M / 4M INFO General (main.cpp : 76) Loading config from /home/ctmr/projects/Aron/SPAdes/output/PA18/corrected/configs/config.info
0:00:00.006 4M / 4M INFO General (main.cpp : 78) Maximum # of threads to use (adjusted due to OMP capabilities): 16
0:00:00.006 4M / 4M INFO General (memory_limit.cpp : 49) Memory limit set to 250 Gb
0:00:00.006 4M / 4M INFO General (main.cpp : 86) Trying to determine PHRED offset
0:00:00.018 4M / 4M INFO General (main.cpp : 92) Determined value is 33
0:00:00.030 4M / 4M INFO General (hammer_tools.cpp : 36) Hamming graph threshold tau=1, k=21, subkmer positions = [ 0 10 ]
0:00:00.031 4M / 4M INFO General (main.cpp : 113) Size of aux. kmer data 24 bytes
=== ITERATION 0 begins ===
0:00:00.031 4M / 4M INFO K-mer Counting (kmer_data.cpp : 280) Estimating k-mer count
0:00:00.200 260M / 260M INFO K-mer Counting (kmer_data.cpp : 285) Processing /home/ctmr/projects/Aron/SPAdes/input/PA18_R1.filtered_human.fq.gz
0:00:34.945 320M / 320M INFO K-mer Counting (kmer_data.cpp : 294) Processed 12646899 reads
0:00:34.946 320M / 320M INFO K-mer Counting (kmer_data.cpp : 285) Processing /home/ctmr/projects/Aron/SPAdes/input/PA18_R2.filtered_human.fq.gz
0:01:08.169 320M / 320M INFO K-mer Counting (kmer_data.cpp : 294) Processed 25293798 reads
0:01:08.169 320M / 320M INFO K-mer Counting (kmer_data.cpp : 299) Total 25293798 reads processed
0:01:08.803 320M / 320M INFO K-mer Counting (kmer_data.cpp : 306) Estimated 255030583 distinct kmers
0:01:08.834 64M / 320M INFO K-mer Counting (kmer_data.cpp : 311) Filtering singleton k-mers
37 8 0
nslots: 536870912
bits per slot: 8 range: 0000002000000000
0:01:08.834 716M / 716M INFO K-mer Counting (kmer_data.cpp : 317) Processing /home/ctmr/projects/Aron/SPAdes/input/PA18_R1.filtered_human.fq.gz
0:05:59.589 716M / 716M INFO K-mer Counting (kmer_data.cpp : 326) Processed 12646899 reads
0:05:59.589 716M / 716M INFO K-mer Counting (kmer_data.cpp : 317) Processing /home/ctmr/projects/Aron/SPAdes/input/PA18_R2.filtered_human.fq.gz
Appreciate any help you can provide
The text was updated successfully, but these errors were encountered:
Did you do any sort of quality control/trimming before running metaspades? I was having this same issue with some of my samples WITH quality filtering using fastp, and after trying again WITHOUT quality filtering then all my samples finished assembly successfully
Hello, I've used SPAdes to assemble my metagenomic datasets however two of my samples are getting stuck in the exact same place repeatedly. I was able to assemble all my samples using megahit without any issues but much prefer SPAdes.
Appreciate any help you can provide
The text was updated successfully, but these errors were encountered: