Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • seq_GA
    Senior Member
    • Feb 2009
    • 124

    BWA error

    I am trying to map solexa pair end reads using BWA.
    1. As the first step, I converted solexa fastq format into sanger fastq using maq.
    Code:
    maq-0.7.1/maq sol2sanger s_5_2_sequence.txt s_5_2_fastq.txt
    2. I build the indices for BWA for human genome
    Code:
    BWA/bwa-0.5.6/bwa index -a bwtsw -p hg18 hg18.fa
    3. Next step is to generate suffice array coordiantes for read1 as below:
    Code:
     BWA/bwa-0.5.6/bwa aln /BWA/Genomes/hg18/hg18.fa s_5_1_fastq.txt > s_5_1.sai
    I am getting error as below.
    Code:
    [bwa_aln] 17bp reads: max_diff = 2
    [bwa_aln] 38bp reads: max_diff = 3
    [bwa_aln] 64bp reads: max_diff = 4
    [bwa_aln] 93bp reads: max_diff = 5
    [bwa_aln] 124bp reads: max_diff = 6
    [bwa_aln] 157bp reads: max_diff = 7
    [bwa_aln] 190bp reads: max_diff = 8
    [bwa_aln] 225bp reads: max_diff = 9
    [bwt_restore_bwt] fail to open file '/BWA/Genomes/hg18/hg18.fa.bwt'. Abort!
    Aborted
    I have all the fasta as well as built indices under the same directory as below:
    hg18.fa
    hg18.pac
    hg18.ann
    hg18.amb
    hg18.rpac
    hg18.bwt
    hg18.rbwt
    hg18.sa
    hg18.rsa

    Anything wrong with this or do I have to move hg18.fa out of this directory? Thanks.
  • nilshomer
    Nils Homer
    • Nov 2008
    • 1283

    #2
    If you used "hg18" as your prefix in your "bwa index" step, you should use the same prefix in your "bwa aln" step:
    Code:
     BWA/bwa-0.5.6/bwa aln /BWA/Genomes/hg18/hg18 s_5_1_fastq.txt > s_5_1.sai
    Ideally, you would not specify "-p" (unless of course you use both Illumina and ABI SOLiD data).

    Comment

    • seq_GA
      Senior Member
      • Feb 2009
      • 124

      #3
      Thanks and it works.

      Comment

      • seq_GA
        Senior Member
        • Feb 2009
        • 124

        #4
        For a pair end read, I tried as below:
        Code:
        BWA/bwa-0.5.6/bwa aln /BWA/Genomes/hg18/hg18 s_5_1_fastq.txt > s_5_1.sai
        BWA/bwa-0.5.6/bwa aln /BWA/Genomes/hg18/hg18 s_5_2_fastq.txt > s_5_2.sai
        
        BWA/bwa-0.5.6/bwa sampe BWA/Genomes/hg18/hg18 s_5_1.sai s_5_2.sai s_5_1_fastq.txt s_5_2_fastq.txt > out.sam
        I get the following error:
        Code:
        [bwa_read_seq] 0.0% bases are trimmed.
        [bwa_read_seq] 0.0% bases are trimmed.
        [bwa_sai2sam_pe_core] convert to sequence coordinate... 
         Segmentation fault
        How to resolve the issue? Thanks.
        Last edited by seq_GA; 05-24-2010, 09:26 PM.

        Comment

        • nilshomer
          Nils Homer
          • Nov 2008
          • 1283

          #5
          Originally posted by seq_GA View Post
          For a pair end read, I tried as below:
          Code:
          BWA/bwa-0.5.6/bwa aln /BWA/Genomes/hg18/hg18 s_5_1_fastq.txt > s_5_1.sai
          BWA/bwa-0.5.6/bwa aln /BWA/Genomes/hg18/hg18 s_5_2_fastq.txt > s_5_2.sai
          
          BWA/bwa-0.5.6/bwa sampe BWA/Genomes/hg18/hg18 s_5_1.sai s_5_2.sai s_5_1_fastq.txt s_5_2_fastq.txt > out.sam
          I get the following error:
          Code:
          [bwa_read_seq] 0.0% bases are trimmed.
          [bwa_read_seq] 0.0% bases are trimmed.
          [bwa_sai2sam_pe_core] convert to sequence coordinate...
          How to resolve the issue? Thanks.
          What's the error (the above is a status message)? Did it not finish?

          Comment

          • seq_GA
            Senior Member
            • Feb 2009
            • 124

            #6
            I was trying to edit my post.. You are too fast.. Anyway I get segmentation fault. Thanks.

            Comment

            • nilshomer
              Nils Homer
              • Nov 2008
              • 1283

              #7
              Originally posted by seq_GA View Post
              I was trying to edit my post.. You are too fast.. Anyway I get segmentation fault. Thanks.
              Sounds like a bug. Did you try sending an email to the BWA mailing list or author (lh3 is his handle on seqanswers)?

              Comment

              • seq_GA
                Senior Member
                • Feb 2009
                • 124

                #8
                I am not able to join the mailing list and post because of some error.
                I am trying to contenate all fasta of hg18 as hg18.fa and then build index. Anything wrong in that approach?

                Comment

                • drio
                  Senior Member
                  • Oct 2008
                  • 323

                  #9
                  Originally posted by seq_GA View Post
                  I am not able to join the mailing list and post because of some error.
                  I am trying to contenate all fasta of hg18 as hg18.fa and then build index. Anything wrong in that approach?
                  You are using an old version of bwa. Please update to -svn or get the latest release.
                  -drd

                  Comment

                  • seq_GA
                    Senior Member
                    • Feb 2009
                    • 124

                    #10
                    Hi,
                    Thx for the response. I am using bwa-0.5.6 and I am upgrading to latest version available bwa-0.5.7. How to check out the version from svn? Can you please provide me the link? Thanks.

                    Comment

                    • nilshomer
                      Nils Homer
                      • Nov 2008
                      • 1283

                      #11
                      Originally posted by seq_GA View Post
                      Hi,
                      Thx for the response. I am using bwa-0.5.6 and I am upgrading to latest version available bwa-0.5.7. How to check out the version from svn? Can you please provide me the link? Thanks.
                      Here's the command. Make sure you have subversion installed:
                      Code:
                      svn co http://bio-bwa.svn.sourceforge.net/svnroot/bio-bwa bio-bwa

                      Comment

                      • seq_GA
                        Senior Member
                        • Feb 2009
                        • 124

                        #12
                        Thx for the info.

                        Comment

                        • drio
                          Senior Member
                          • Oct 2008
                          • 323

                          #13
                          Originally posted by seq_GA View Post
                          Hi,
                          Thx for the response. I am using bwa-0.5.6 and I am upgrading to latest version available bwa-0.5.7. How to check out the version from svn? Can you please provide me the link? Thanks.
                          If you want to avoid svn (I'd suggest you don't), from here:



                          click in SF download page. That will take you to the latest release (already binary).

                          ALso, perhaps you can tell Heng how you got to the older version. I think there are some links there that still point to old versions.
                          -drd

                          Comment

                          • seq_GA
                            Senior Member
                            • Feb 2009
                            • 124

                            #14
                            Hi,
                            i get the same error even if I use the build from svn..

                            Comment

                            • drio
                              Senior Member
                              • Oct 2008
                              • 323

                              #15
                              Run your binary via gdb:

                              Code:
                              $ gdb your_bwa_binary
                              .... gdb output ... 
                              > run sampe BWA/Genomes/hg18/hg18 s_5_1.sai s_5_2.sai s_5_1_fastq.txt s_5_2_fastq.txt > out.sam
                              .... gdb output ....
                              > bt
                              And show us the output.
                              -drd

                              Comment

                              Latest Articles

                              Collapse

                              • SEQadmin2
                                Nine Things a Sample Prep Scientist Thinks About Before Sequencing
                                by SEQadmin2


                                I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.


                                Here are nine questions we think about, in roughly the order they matter, before...
                                06-18-2026, 07:11 AM
                              • SEQadmin2
                                From Collection to Sequencing: Why Sample Preparation and Preservation Define Sequencing Data
                                by SEQadmin2


                                Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.


                                The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
                                ...
                                06-02-2026, 10:05 AM
                              • SEQadmin2
                                Single-Cell Sequencing at an Inflection Point: Early Impacts of New Platforms and Emerging Trends
                                by SEQadmin2


                                With the launch of new single-cell sequencing platforms in 2026, the field stands at an exciting inflection point. This article surveys the most impactful advances in the field and discusses how they’re reshaping research in cancer, immunology, and beyond.


                                Introduction

                                Single-cell sequencing technologies have undergone remarkable advances over the past decade, transitioning from low-throughput experimental approaches to highly scalable platforms capable of...
                                05-22-2026, 06:42 AM

                              ad_right_rmr

                              Collapse

                              News

                              Collapse

                              Topics Statistics Last Post
                              Started by SEQadmin2, 06-17-2026, 06:09 AM
                              0 responses
                              21 views
                              0 reactions
                              Last Post SEQadmin2  
                              Started by SEQadmin2, 06-09-2026, 11:58 AM
                              0 responses
                              39 views
                              0 reactions
                              Last Post SEQadmin2  
                              Started by SEQadmin2, 06-05-2026, 10:09 AM
                              0 responses
                              46 views
                              0 reactions
                              Last Post SEQadmin2  
                              Started by SEQadmin2, 06-04-2026, 08:59 AM
                              0 responses
                              49 views
                              0 reactions
                              Last Post SEQadmin2  
                              Working...