Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • How to check for mutations common across all samples?

    I have .bam, .vcf, and ANNOVAR .csv files for several samples.

    Is there a straightforward way to sort or view mutations that are the most common or present in several samples?

    I was thinking of trying to sort the variant location columns in ascending order and line them up for all the samples, but then how would I create a list of the most common variants?

    Any ideas are appreciated, thank you.

  • #2
    I had to do this once. It's not a perfect solution, but check out this thread: Get common lines from multiple files. Specifically, look at what the user Radoulov posts. Unfortunately, the solution is just provided and not explained so it might be hard to tweak it.

    You'll probably have to take out a few columns of your vcf though. If you just want the chrom, pos and alt, you could do:
    Code:
    awk '{print $1,$2,$5}' file.vcf
    I'm sure there are some other things that you would have to do with the output if it's not exactly what you want, but I think it can be done with a few unix commands.

    Edit: One more thing. If you wanted to do several pairwise comparisons (which you probably don't), look into using unix's comm.
    Last edited by blakeoft; 07-16-2014, 12:14 PM.

    Comment


    • #3
      Thank you for the help, I was able to do something with what you suggested.

      It looks like many of the samples have tons of the same mutations so I'm not sure how fruitful this little test was. Perhaps I can refine it.

      Comment


      • #4
        You might also filter out the variants in dbsnp, or at least do them separately.

        Comment


        • #5
          Programs like BEDTools can give you the intersection of multiple .vcf files.

          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, Today, 08:47 AM
          0 responses
          10 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-11-2024, 12:08 PM
          0 responses
          60 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 10:19 PM
          0 responses
          59 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 09:21 AM
          0 responses
          53 views
          0 likes
          Last Post seqadmin  
          Working...
          X