Skip to content
New issue

Have a question about this project? Sign up for a free GitHub account to open an issue and contact its maintainers and the community.

By clicking “Sign up for GitHub”, you agree to our terms of service and privacy statement. We’ll occasionally send you account related emails.

Already on GitHub? Sign in to your account

Segmentation fault while reading fastq files #51

Closed
abshah opened this issue Sep 12, 2018 · 1 comment
Closed

Segmentation fault while reading fastq files #51

abshah opened this issue Sep 12, 2018 · 1 comment

Comments

@abshah
Copy link

abshah commented Sep 12, 2018

Hi SOAPdenovo2 dev team,
I would like to report a strange issue in the initial stages of running SOAPdenovo2. The program exits with a segmentation fault and core dump.

The error looks like this

183578 Memory Access Error (Memory Dump Written)

My stdout looks like this :

Version 2.04: released on July 13th, 2012
Compile Jan 27 2015     11:50:30

********************
Pregraph
********************

Parameters: pregraph -s /data/idiv_schielzeth/Grasshoppers/Gsib_Green_Brown_HiSeqX_libs_2018/F18FTSEUHT0360_G.SbluR/raw_reads/G.sibiricusGreen/assembly/Gsib_GB_final_assembly/config_G.sibGB_half_paired.txt -K 43 -p 16 -R -o assembly_G.sibGB_half_assembly3

In /data/idiv_schielzeth/Grasshoppers/Gsib_Green_Brown_HiSeqX_libs_2018/F18FTSEUHT0360_G.SbluR/raw_reads/G.sibiricusGreen/assembly/Gsib_GB_final_assembly/config_G.sibGB_half_paired.txt, 1 lib(s), maximum read length 150, maximum name length 256.

16 thread(s) initialized.
Import reads from file:
 /data/idiv_schielzeth/Grasshoppers/Bielefeld/Gsib_GB_HiSeqX_final_satminer_run/subsampled/Gsib_GB_R1_half_sample.fastq
Import reads from file:
 /data/idiv_schielzeth/Grasshoppers/Bielefeld/Gsib_GB_HiSeqX_final_satminer_run/subsampled/Gsib_GB_R2_half_sample.fastq
--- 100000000th reads.
--- 200000000th reads.
--- 300000000th reads.

My config file looks like this

#maximal read length
max_rd_len=150
[LIB]
#average insert size
avg_ins=250
#if sequence needs to be reversed
reverse_seq=0
#in which part(s) the reads are used
asm_flags=3
#use only first 100 bps of each read
rd_len_cutoff=150
#in which order the reads are used while scaffolding
rank=1
#cutoff of pair number for a reliable connection (at least 3 for short insert size)
pair_num_cutoff=3
#minimum aligned length to contigs for a reliable read location (at least 32 for short insert size)
map_len=32
#a pair of fastq file, read 1 file should always be followed by read 2 file
q1=/data/idiv_schielzeth/Grasshoppers/Bielefeld/Gsib_GB_HiSeqX_final_satminer_run/subsampled/Gsib_GB_R1_half_sample.fastq
q2=/data/idiv_schielzeth/Grasshoppers/Bielefeld/Gsib_GB_HiSeqX_final_satminer_run/subsampled/Gsib_GB_R2_half_sample.fastq


@aquaskyline
Copy link
Owner

It's a running environment-related error. I don't have any clue about what happened.

Sign up for free to join this conversation on GitHub. Already have an account? Sign in to comment
Labels
None yet
Projects
None yet
Development

No branches or pull requests

2 participants