Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Deb
    Junior Member
    • Nov 2011
    • 4

    #1

    Picard: EstimateLibraryComplexity

    Hello,

    I've been using EstimateLibraryComplexity in Picard and have read the documentation but want to make sure I am interpreting the results accurately. We recently ran an estimate on our genomic reads and our library size was reported as 660,102,280 while the number of read pairs was 170,440,606 (our genome size is ~1GB). From my interpretation, this means that we have 660,102,280 unique fragments within our library of which 170,440,606 have been sequenced. Therefore, we have sequenced ~1/3 of the library and in theory some additional HiSeq runs would be needed to increase complexity?

    Any insight would be helpful.

    Thank you!
  • timydaley
    Member
    • Jun 2010
    • 26

    #2
    If you want to get more distinct genomic molecules from the library, then sequencing more will give you more. But there is a law of diminishing returns since you have already sequenced the most common molecules in the library, so that most of the additional sequencing is duplicates. I am not sure how Picard estimates the library size, looking at the java code now, but it doesn't answer the question of how much more you stuff you will get from sequencing more.

    Our lab does a lot of bisulfite sequencing analysis. To save money on sequencing poor libraries, we developed a tool to answer this question, "How many more reads are you going to get?" The website is here. Since we were looking at mapped reads, this is what the input is. We're looking for users, so maybe this can be of help to your problem.

    Comment

    Latest Articles

    Collapse

    • SEQadmin2
      Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
      by SEQadmin2



      CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

      Despite this, “CRISPR helped turn genome editing from a specialized technique into
      ...
      07-31-2026, 11:01 AM
    • SEQadmin2
      Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
      by SEQadmin2


      Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

      The systematic characterization of the human proteome has
      ...
      07-20-2026, 11:48 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by SEQadmin2, 08-13-2026, 12:22 PM
    0 responses
    29 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-11-2026, 10:35 AM
    0 responses
    24 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-06-2026, 07:41 AM
    0 responses
    38 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-03-2026, 10:13 AM
    0 responses
    51 views
    0 reactions
    Last Post SEQadmin2  
    Working...