Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • castrovr
    Junior Member
    • Nov 2016
    • 7

    Merge paired-end sequences

    Hello

    I'm new and I wonder if somebody knows is the program fastq-join requires perfect matches to merged the reads.
    Maybe is obvious but I need to be sure of this information.

    Thank you
  • Brian Bushnell
    Super Moderator
    • Jan 2014
    • 2709

    #2
    No, it does not. However, I've found that fastq-join does not give very good results in my tests, compared to other programs such as BBMerge (which I wrote) and Usearch.

    Comment

    • castrovr
      Junior Member
      • Nov 2016
      • 7

      #3
      Brian

      Thank you for your quick reply. I will try BBMerge and Usearch with my sequences and compare the results.

      Ruth

      Comment

      • castrovr
        Junior Member
        • Nov 2016
        • 7

        #4
        BBmerge stats.sh

        Hello
        I download and installed BBmap, and I tried to test the stat.sh of BBmerge but I had an error:
        Exception in thread "main" java.lang.UnsupportedClassVersionError: Bad version number in .class file
        at java.lang.ClassLoader.defineClass1(Native Method)
        at java.lang.ClassLoader.defineClass(Unknown Source)
        at java.security.SecureClassLoader.defineClass(Unknown Source)
        at java.net.URLClassLoader.defineClass(Unknown Source)
        at java.net.URLClassLoader.access$100(Unknown Source)
        at java.net.URLClassLoader$1.run(Unknown Source)
        at java.security.AccessController.doPrivileged(Native Method)
        at java.net.URLClassLoader.findClass(Unknown Source)
        at java.lang.ClassLoader.loadClass(Unknown Source)
        at sun.misc.Launcher$AppClassLoader.loadClass(Unknown Source)
        at java.lang.ClassLoader.loadClass(Unknown Source)
        at java.lang.ClassLoader.loadClassInternal(Unknown Source)
        Full Command:/local/cluster/spatafora/bin/bbmap/stats.sh in=/local/cluster/spatafora/bin/bbmap/resources/phix174_ill.ref.fa.gz

        What's this error means?

        Comment

        • GenoMax
          Senior Member
          • Feb 2008
          • 7142

          #5
          Originally posted by castrovr View Post
          Hello
          I download and installed BBmap, and I tried to test the stat.sh of BBmerge but I had an error:
          Exception in thread "main" java.lang.UnsupportedClassVersionError: Bad version number in .class file
          at java.lang.ClassLoader.defineClass1(Native Method)
          at java.lang.ClassLoader.defineClass(Unknown Source)
          at java.security.SecureClassLoader.defineClass(Unknown Source)
          at java.net.URLClassLoader.defineClass(Unknown Source)
          at java.net.URLClassLoader.access$100(Unknown Source)
          at java.net.URLClassLoader$1.run(Unknown Source)
          at java.security.AccessController.doPrivileged(Native Method)
          at java.net.URLClassLoader.findClass(Unknown Source)
          at java.lang.ClassLoader.loadClass(Unknown Source)
          at sun.misc.Launcher$AppClassLoader.loadClass(Unknown Source)
          at java.lang.ClassLoader.loadClass(Unknown Source)
          at java.lang.ClassLoader.loadClassInternal(Unknown Source)
          Full Command:/local/cluster/spatafora/bin/bbmap/stats.sh in=/local/cluster/spatafora/bin/bbmap/resources/phix174_ill.ref.fa.gz

          What's this error means?
          Do you know which version of Java you are using? @Brian validates BBMap against Java 7/8 (not sure if 6 is supported any more).

          Comment

          • Brian Bushnell
            Super Moderator
            • Jan 2014
            • 2709

            #6
            Java 6 does work for most of the programs (except BBNorm), though I don't test with it anymore. This error message looks like it's from Java 5 or earlier. Please try running this, on the command line:

            Code:
            java -Xmx100m -version

            Comment

            • castrovr
              Junior Member
              • Nov 2016
              • 7

              #7
              Yes, it seems I was using an older version of Java, I change that and run the test and it works!. Now I running my own data. No error messages yet.
              Thank you

              Comment

              • castrovr
                Junior Member
                • Nov 2016
                • 7

                #8
                Create a short insert library in silico

                Hello all,

                I have I genome assembly that I made with velvet, and now I want to create in silico a short insert library of ~250pb. Which program in your experience is better to do this?

                Thanks

                Comment

                • Brian Bushnell
                  Super Moderator
                  • Jan 2014
                  • 2709

                  #9
                  I'd suggest RandomReads. You can use it like this:

                  (index the reference)
                  bbmap.sh ref=assembly.fa

                  (generate reads)
                  randomreads.sh out=reads.fq.gz reads=5m paired len=100 mininsert=150 maxinsert=350 bell adderrors

                  That will get a 250bp insert average, with a bell-shaped distribution, and 100bp reads. The file will be interleaved but you can get reads in 2 files with the out1 and out2 flags if you want.

                  Comment

                  • castrovr
                    Junior Member
                    • Nov 2016
                    • 7

                    #10
                    Thank you Brian

                    Comment

                    Latest Articles

                    Collapse

                    • GATTACAT
                      Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
                      by GATTACAT
                      Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
                      Today, 11:43 AM
                    • 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

                    ad_right_rmr

                    Collapse

                    News

                    Collapse

                    Topics Statistics Last Post
                    Started by SEQadmin2, Yesterday, 05:37 AM
                    0 responses
                    8 views
                    0 reactions
                    Last Post SEQadmin2  
                    Started by SEQadmin2, 06-26-2026, 11:10 AM
                    0 responses
                    17 views
                    0 reactions
                    Last Post SEQadmin2  
                    Started by SEQadmin2, 06-17-2026, 06:09 AM
                    0 responses
                    52 views
                    0 reactions
                    Last Post SEQadmin2  
                    Started by SEQadmin2, 06-09-2026, 11:58 AM
                    0 responses
                    110 views
                    0 reactions
                    Last Post SEQadmin2  
                    Working...