Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • How to isolate and examine discordant pairs?

    Hello,
    I am examining yeast that have undergone meiotic recombination, using paired-end sequencing on the Illumina MiSeq and aligned with bowtie2.
    I want to look in my sequencing data for ectopic recombination, e.g. if one read pair mate aligns to one chromosome and the other mate to another chromosome. I think I can do this by isolating 'discordant' pairs, e.g. in the command line output you get something like:

    650 pairs aligned concordantly 0 times; of these:
    34 (5.23%) aligned discordantly 1 time

    I want to be able to isolate and take a closer look at the discordant pairs, but I can't figure out how they are marked in the SAM file - I have been reading about the CIGAR string and FLAG field, but I don't think any of the values match what I want.

    Many thanks for any help with this

  • #2
    The FLAG field has bit 0x2 set if reads are properly paired. So, you want to filter for reads that have bit 0x2 unset. For example, with Reformat:

    reformat.sh in=mapped.sam out=filtered.sam requiredbits=1 filterbits=14

    That will require reads to have a mate (1) and forbid them from being properly paired, unmapped, or having an unmapped mate (2 & 4 & 8 = 14).

    You can do the same thing with samtools -f and -F flags.

    Comment


    • #3
      Originally posted by Brian Bushnell View Post
      The FLAG field has bit 0x2 set if reads are properly paired. So, you want to filter for reads that have bit 0x2 unset. For example, with Reformat:

      reformat.sh in=mapped.sam out=filtered.sam requiredbits=1 filterbits=14

      That will require reads to have a mate (1) and forbid them from being properly paired, unmapped, or having an unmapped mate (2 & 4 & 8 = 14).

      You can do the same thing with samtools -f and -F flags.
      Thank you very much for your reply!

      I am now trying to run bbmap reformat on Windows via the command line by entering:

      java -ea -Xmx200m C:\bbmap\current\ jgi.ReformatReads in=reads.sam out=discordant.sam requiredbits=1 filterbits=14

      However, I get the error: "Could not find or load main class C:\bbmap\current\". From googling the error it seems there is probably something wrong with the filepath but I tried a few different things and it still doesn't work. I'm not very experienced with java!

      Comment


      • #4
        Is your BBMap directory under c:\? If you put it someplace else then replace the c:\ with that path (e.g. c:\download\bbmap\current).

        Comment


        • #5
          Originally posted by GenoMax View Post
          Is your BBMap directory under c:\? If you put it someplace else then replace the c:\ with that path (e.g. c:\download\bbmap\current).
          Yes, it is under C:\ (I deliberately put it there to make the path nice and short )

          Comment


          • #6
            There should be a space between C:\bbmap\current\ and jgi.ReformatReads. Is it there? Hard to tell from post. Hopefully you did not move any files under bbmap folder.

            Comment


            • #7
              Originally posted by GenoMax View Post
              There should be a space between C:\bbmap\current\ and jgi.ReformatReads. Is it there? Hard to tell from post. Hopefully you did not move any files under bbmap folder.
              Yes, there is a space. I didn't move any files either, but I might try re-downloading bbmap just in case.

              Comment


              • #8
                I am not that good at Java either but I do think you need a 'cp' before your path. When I run 'reformat.sh' from a Linux command line it says that it is running the program like so (single line broken down into multiple lines for clarity)

                java
                -ea
                -Xmx200m
                -cp /group/bioinfo/apps/apps/BBMap-34.94/current/
                jgi.ReformatReads
                PhiX_NoIndexfastq.gz
                out=rick.tmp

                Comment


                • #9
                  Originally posted by westerman View Post
                  I am not that good at Java either but I do think you need a 'cp' before your path. When I run 'reformat.sh' from a Linux command line it says that it is running the program like so (single line broken down into multiple lines for clarity)

                  java
                  -ea
                  -Xmx200m
                  -cp /group/bioinfo/apps/apps/BBMap-34.94/current/
                  jgi.ReformatReads
                  PhiX_NoIndexfastq.gz
                  out=rick.tmp
                  Thanks so much! Adding '-cp' works. However... it now can't find my .sam file. Which folder is it looking in? I tried putting the file in the 'bbmap', 'current' and 'jgi' folders. Or do I need the full path in front of each filename as well?

                  Comment


                  • #10
                    The full path couldn't hurt. Quoting for spaces, etc. if you have any.

                    Comment


                    • #11
                      OK, I added the full path to each filename and it works now! Thanks for all the help in this thread

                      Comment

                      Latest Articles

                      Collapse

                      • seqadmin
                        Recent Advances in Sequencing Analysis Tools
                        by seqadmin


                        The sequencing world is rapidly changing due to declining costs, enhanced accuracies, and the advent of newer, cutting-edge instruments. Equally important to these developments are improvements in sequencing analysis, a process that converts vast amounts of raw data into a comprehensible and meaningful form. This complex task requires expertise and the right analysis tools. In this article, we highlight the progress and innovation in sequencing analysis by reviewing several of the...
                        05-06-2024, 07:48 AM
                      • 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

                      ad_right_rmr

                      Collapse

                      News

                      Collapse

                      Topics Statistics Last Post
                      Started by seqadmin, 05-10-2024, 06:35 AM
                      0 responses
                      20 views
                      0 likes
                      Last Post seqadmin  
                      Started by seqadmin, 05-09-2024, 02:46 PM
                      0 responses
                      26 views
                      0 likes
                      Last Post seqadmin  
                      Started by seqadmin, 05-07-2024, 06:57 AM
                      0 responses
                      21 views
                      0 likes
                      Last Post seqadmin  
                      Started by seqadmin, 05-06-2024, 07:17 AM
                      0 responses
                      21 views
                      0 likes
                      Last Post seqadmin  
                      Working...
                      X