Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Ion Torrent targeted sequencing

    Hello Every one,

    I am a new NGS user. I am starting to work on targeted sequencing using Ion Torrent technology.

    My targeted gene is BRCA1 and I have about 50 samples. The gene is 112 amplicon. I would like to know how many samples per run I can pool?

    Thank you for your help

  • #2
    That depends a little on your experiment, ie how big your amplicons are, if its germline somatic mutationd and which chip you want to use ie 314/316/318.
    FYI -- we have recently been testing Sabioscience (Qiagen) gene-read (multiplex PCR) for this type of targeted experiment, seems to work well. We estimate (guess-timate) that 48 samples should be reasonable on a 316 (200mbp) Ion run.

    Comment


    • #3
      Thank you for your replay.
      I was just wondering how do you do these calculations?

      I found out that if I used 318 I will get a coverage of 7,84 but should use tow chips as the chip takes 48 samples. on the other hand if I used 316 I will have a coverage of 1,57. My samples are DNA from blood, do I need still (big) coverage?

      Comment


      • #4
        Here's a back-of-the-envelope calculation (i.e. it's rough).

        Assuming that average amplicon size = 200 bp
        you have 112 amplicons,
        you want 100X seq coverage

        = 2,2 mbp/individual (ie 200bp X 112 amplicons X 100 fold).

        2,2 X 48 = 107 mbp total. ABout capacity of a 316 mbp

        Very rough though so maybe overestimate needed coverage in order to achieve the minimum you need (ie difference in amplicons, barcodes etc).

        Comment


        • #5
          Thank you

          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, 04-11-2024, 12:08 PM
          0 responses
          59 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 10:19 PM
          0 responses
          57 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 09:21 AM
          0 responses
          51 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-04-2024, 09:00 AM
          0 responses
          55 views
          0 likes
          Last Post seqadmin  
          Working...
          X