Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • tophat2 splice sequence has more than 2^32-1 characters

    Hello,

    I have 60 samples that I've tried on tophat2 and about half have all failed at Indexing splices saying "Error: Reference sequence has more than 2^32-1 characters".

    Anyone else get this and have a solution? Any ideas?

    Comand used:

    Code:
     
    ${TOPHAT} \
    --mate-inner-dist ${INNERDIST} \
    --mate-std-dev ${STDEV} \
    --output-dir $PBS_O_WORKDIR/tophat2 \
    --num-threads 12 \
    --transcriptome-index ${HUMAN_TRANS_FA} \
    --no-coverage-search \
    --fusion-search \
    --fusion-ignore-chromosomes MT \
    --b2-sensitive \
    --keep-fasta-order \
    --rg-id ${SAMPLE_ID}_${DATE} \
    --rg-sample ${SAMPLE_ID} \
    --rg-library ${SAMPLE_ID}_Lib1 \
    --rg-platform ILLUMINA \
    ${HUMAN_REF_FA} \
    ${read1} ${read2}
    And error output:

    Code:
    [2012-07-19 00:40:43] Beginning TopHat run (v2.0.4)
    -----------------------------------------------
    [2012-07-19 00:40:43] Checking for Bowtie
    		  Bowtie version:	 2.0.0.7
    [2012-07-19 00:40:43] Checking for Samtools
    		Samtools version:	 0.1.18.0
    [2012-07-19 00:40:43] Checking for Bowtie index files
    [2012-07-19 00:40:43] Checking for Bowtie index files
    [2012-07-19 00:40:43] Checking for reference FASTA file
    [2012-07-19 00:40:43] Generating SAM header for ~/resources/GRCh37/bowtie2_b37/Homo_sapiens.GRCh37.62
    	format:		 fastq
    	quality scale:	 phred33 (default)
    [2012-07-19 00:41:19] Reading known junctions from GTF file
    [2012-07-19 00:41:33] Preparing reads
    	 left reads: min. length=51, max. length=51, 82100145 kept reads (7919 discarded)
    	right reads: min. length=51, max. length=51, 81990155 kept reads (117909 discarded)
    [2012-07-19 01:11:51] Using pre-built transcriptome index..
    [2012-07-19 01:11:57] Mapping left_kept_reads to transcriptome Homo_sapiens.GRCh37.66 with Bowtie2 
    [2012-07-19 02:28:44] Mapping right_kept_reads to transcriptome Homo_sapiens.GRCh37.66 with Bowtie2 
    [2012-07-19 03:44:34] Resuming TopHat pipeline with unmapped reads
    [2012-07-19 03:44:34] Mapping left_kept_reads.m2g_um to genome Homo_sapiens.GRCh37.62 with Bowtie2 
    [2012-07-19 03:59:51] Mapping left_kept_reads.m2g_um_seg1 to genome Homo_sapiens.GRCh37.62 with Bowtie2 (1/2)
    [2012-07-19 04:02:30] Mapping left_kept_reads.m2g_um_seg2 to genome Homo_sapiens.GRCh37.62 with Bowtie2 (2/2)
    [2012-07-19 04:05:18] Mapping right_kept_reads.m2g_um to genome Homo_sapiens.GRCh37.62 with Bowtie2 
    [2012-07-19 04:20:59] Mapping right_kept_reads.m2g_um_seg1 to genome Homo_sapiens.GRCh37.62 with Bowtie2 (1/2)
    [2012-07-19 04:24:50] Mapping right_kept_reads.m2g_um_seg2 to genome Homo_sapiens.GRCh37.62 with Bowtie2 (2/2)
    [2012-07-19 04:28:48] Searching for junctions via segment mapping
    [2012-07-19 05:04:34] Retrieving sequences for splices
    [2012-07-19 05:18:32] Indexing splices
    Error: Reference sequence has more than 2^32-1 characters!  Please divide the
    reference into batches or chunks of about 3.6 billion characters or less each
    and index each independently.
    Error: Encountered internal Bowtie 2 exception (#1)

  • #2
    Turns out this was due to an upgrade to our isilon NFS disk... Rebooting machines fixed the error. Very strange, but moving on...

    Comment

    Latest Articles

    Collapse

    • seqadmin
      Essential Discoveries and Tools in Epitranscriptomics
      by seqadmin




      The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...
      04-22-2024, 07:01 AM
    • seqadmin
      Current Approaches to Protein Sequencing
      by seqadmin


      Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
      04-04-2024, 04:25 PM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by seqadmin, Yesterday, 11:49 AM
    0 responses
    15 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-24-2024, 08:47 AM
    0 responses
    16 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-11-2024, 12:08 PM
    0 responses
    61 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 10:19 PM
    0 responses
    60 views
    0 likes
    Last Post seqadmin  
    Working...
    X