Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • jylee
    Junior Member
    • Jun 2019
    • 3

    #1

    bbmap.sh: line 352 RANDOM# Killed

    Hello all,

    I keep facing crash while mapping contig files with BBMap(v.38.76). I am running command "bbmap.sh in=sample_r1.fastq in2=sample_r2.fastq out=./sample_bbmapped.sam bamscript=bs.sh" and process stops on "Started 40 mapping threads" as highlighted in quote below. I can only see "bbmap.sh:line 352: random number Killed". I wonder if anyone have had similar issue or know how to fix this. Thank you for your time and consideration!

    May the force be with you,
    Joo-Young



    java -da -Xmx377g -Xms377g -cp /mnt/home/leejooy5/Downloads/bbmap/current/ align2.BBMap build=1 overwrite=true fastareadlen=500 -da -Xmx377g in=Std_host_removed_R1.fastq in2=Std_host_removed_R2.fastq out=./sorted_indexed20200219/Std_megahit_BBmapped.sam bamscript=bs.sh
    Executing align2.BBMap [build=1, overwrite=true, fastareadlen=500, -da, -Xmx377g, in=Std_host_removed_R1.fastq, in2=Std_host_removed_R2.fastq, out=./sorted_indexed20200219/Std_megahit_BBmapped.sam, bamscript=bs.sh]
    Version 38.76

    Retaining first best site only for ambiguous mappings.
    Found samtools 1.9
    Set genome to 1

    Loaded Reference: 0.509 seconds.
    Loading index for chunk 1-1, build 1
    Generated Index: 1.078 seconds.
    Analyzed Index: 2.608 seconds.
    Started output stream: 0.075 seconds.
    Cleared Memory: 0.389 seconds.
    Processing reads in paired-ended mode.
    Started read stream.
    Started 40 mapping threads.
    /mnt/home/leejooy5/Downloads/bbmap/bbmap.sh: line 352: 10803 Killed java -da -Xmx377g -Xms377g -cp /mnt/home/leejooy5/Downloads/bbmap/current/ align2.BBMap build=1 overwrite=true fastareadlen=500 -da -Xmx377g in=Std_host_removed_R1.fastq in2=Std_host_removed_R2.fastq out=./sorted_indexed20200219/Std_megahit_BBmapped.sam bamscript=bs.sh
    Note: This script is designed to run with the amount of memory detected by BBMap.
    If Samtools crashes, please ensure you are running on the same platform as BBMap,
    or reduce Samtools' memory setting (the -m flag).
    Note: Please ignore any warnings about 'EOF marker is absent'; this is a bug in samtools that occurs when using piped input.
    [bam_sort_core] merging from 0 files and 3 in-memory blocks...
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    Cross-posted on biostars: https://www.biostars.org/p/423541/

    I will keep answering there.

    Comment

    Latest Articles

    Collapse

    • SEQadmin2
      Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
      by SEQadmin2



      CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

      Despite this, “CRISPR helped turn genome editing from a specialized technique into
      ...
      07-31-2026, 11:01 AM
    • SEQadmin2
      Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
      by SEQadmin2


      Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

      The systematic characterization of the human proteome has
      ...
      07-20-2026, 11:48 AM
    • SEQadmin2
      Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
      by SEQadmin2



      Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
      ...
      07-09-2026, 11:10 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by SEQadmin2, Yesterday, 07:41 AM
    0 responses
    12 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-03-2026, 10:13 AM
    0 responses
    27 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-31-2026, 02:55 AM
    0 responses
    39 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-24-2026, 12:17 PM
    0 responses
    25 views
    0 reactions
    Last Post SEQadmin2  
    Working...