Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • #16
    I have seen duplicate percentage of 33% in targeted high coverage experiment and based on my assessment of false positive and false negative I am happy not removing duplicates.

    Comment


    • #17
      Originally posted by husamia View Post
      I have seen duplicate percentage of 33% in targeted high coverage experiment and based on my assessment of false positive and false negative I am happy not removing duplicates.
      It depends on what your experiment is. In some cases it has very little effect, in some it can be detrimental. In no case that I've heard of does leaving PCR duplicates in your data improve your results, however.
      Mendelian Disorder: A blogshare of random useful information for general public consumption. [Blog]
      Breakway: A Program to Identify Structural Variations in Genomic Data [Website] [Forum Post]
      Projects: U87MG whole genome sequence [Website] [Paper]

      Comment


      • #18
        Originally posted by lh3 View Post
        It is possible to dedup before mapping. You may hash the first 14bp of each end and discard a pair if the 14+14bp coincides another pair. This method is not as good as deduping after mapping, but should be good enough. On the other hand, I do not think deduping is quite necessary for assembly.
        Why 14bp? Why not something else?

        Comment


        • #19
          Hi. everybody
          I have a problem about remove duplicates,
          In this study , http://www.ncbi.nlm.nih.gov/Traces/sra/?study=ERP000603
          It's have 2 Experiments, and 13 RUNs,
          How to do remove duplicates? by study? by Experiments? or by one runs?
          Thanks !!

          Comment


          • #20
            Remove PCR duplicates by library (and this looks like one big "library" mixed from 4 PCR pools). Optical duplicates are removed by lane (but I guess Picard would detect the within lane reads, given proper read group labelling).

            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