Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • sanju0891
    Member
    • Mar 2012
    • 15

    #1

    Short fragments removal- Amplicon sequencing

    Hi
    i have performed amplicon sequencing using gs junior and in the first run they were peaks around 120-150 bp.

    so in the next run i want to reduce these peaks. i did 2x purification with the ampure beads(0.8: 1 ratio) but still there are slight or faint bands visible in agarose gel. How do i get rid of these bands completely?

    if i am purifying it more further i am losing my ampliocns which are around 300bp.

    Please help me.

    Thanks
  • pmiguel
    Senior Member
    • Aug 2008
    • 2328

    #2
    You might be able to drop to a lower ratio. Depends on your lot of beads. If you take a DNA ladder of some sort, you can calibrate your batch of beads by trying different ratios. Here is an example:



    For this calibration, it looks like the best differentiation between 300 and 150 bp would be around 0.7:1 or 0.75:1.

    Alternatively you can just cut your band of a desired size out of a gel and extract the DNA from the slice. But that may be more work. Well, maybe not for a single band. But if you had numerous samples it would be.

    --
    Phillip

    Comment

    • sanju0891
      Member
      • Mar 2012
      • 15

      #3
      Hi
      Thankyou so much for replying

      with the 0.8:1, i was able to remove all bands below 250bp , eventhough there is a slight loss of my amplicon samples.

      but now the problem was with the quantitation of the samples. we used the Nanodrop 2000 to measure the conc of DNA in the purified samples. but the nanodrop values are negative for concentration of DNA.

      i do not understand this and i am confused with wat procedure shuould i use to quatify my samples?

      Comment

      • pmiguel
        Senior Member
        • Aug 2008
        • 2328

        #4
        A nanodrop spectrophotometer is not useful for quantifying samples below 20 ng/ul or so. Use a fluorimeter, a bioanalyzer chip, and/or your gel. Or qPCR.

        --
        Phillip

        Comment

        • sanju0891
          Member
          • Mar 2012
          • 15

          #5
          Thank you for the reply.

          we are thinking to use the picogreen assay fro the quantitation.

          Comment

          • HMorrison
            Senior Member
            • May 2009
            • 121

            #6
            We use picogreen routinely, then make amplicon pools and quantitate the pools with Kapa qPCR kit. Has been very reliable.

            Comment

            • sanju0891
              Member
              • Mar 2012
              • 15

              #7
              i was just reading all the threads and evrybody recomends Kappa kit.

              i have a small question regarding this. which kit from the KAPA biosystems is best fro GS junior titanium- LIB A

              Comment

              • HMorrison
                Senior Member
                • May 2009
                • 121

                #8
                Kapa kits

                I don't know all the variations and it depends on your cycler; check with the company first if you have trouble sorting out their web site (really needs a decision tree).

                We use the FLX version, not the Ti version, with LibA (adapters for LibA/Titanium are like old FLX adapters, not like LibL/Titanium shotgun). Part number is KK4830. This is for ABI Prism qPCR instrument. We have a standard GS-FLX, not Junior.

                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
                • SEQadmin2
                  Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
                  by SEQadmin2



                  Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
                  ...
                  07-09-2026, 11:10 AM

                ad_right_rmr

                Collapse

                News

                Collapse

                Topics Statistics Last Post
                Started by SEQadmin2, Yesterday, 07:41 AM
                0 responses
                12 views
                0 reactions
                Last Post SEQadmin2  
                Started by SEQadmin2, 08-03-2026, 10:13 AM
                0 responses
                25 views
                0 reactions
                Last Post SEQadmin2  
                Started by SEQadmin2, 07-31-2026, 02:55 AM
                0 responses
                38 views
                0 reactions
                Last Post SEQadmin2  
                Started by SEQadmin2, 07-24-2026, 12:17 PM
                0 responses
                25 views
                0 reactions
                Last Post SEQadmin2  
                Working...