Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • CharlesG
    Junior Member
    • Jul 2019
    • 8

    #1

    Advice on how much data output to specify for single Cell RNA seq of human PBMCs?

    Hi everyone, I am a novice in to single cell RNA seq and my colleagues and I have sent PBMCs of one patient (before and after treatment) to Novogene for paired-end single cell RNA sequencing. We are interested in obtaining as much biological information as possible from the sequenced PBMCs including sepration of sub-populations, differential expression analysis, gene-gene correlation or covariation, possible discovery of novel cell types.

    Novogene has sent us an urgent email asking us how much data to output from the PBMCs and also if we need information about the sequencing saturation (we will be charged more for this). They can output between 12 million bp and 50 million bp. My colleagues and I have searched the internet but cannot find exactly which information to provide to Novogene in this regard. Please can any one help us with some advice? So far all we know is that 30000 reads per cell is suffifient to seprate different populations of PBMCs.Thank you in advance for your kind help.
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    Are you using 10x? If so take a look at: https://kb.10xgenomics.com/hc/en-us/...ion-libraries-

    Comment

    • CharlesG
      Junior Member
      • Jul 2019
      • 8

      #3
      Thank you very much for the very helpful suggestion. However I still wish to know how much data output in Giga bases should I specify to Novogene for a 90% sequencing saturation level and 30000 reads per cell?
      Last edited by CharlesG; 04-20-2020, 07:37 AM.

      Comment

      • GenoMax
        Senior Member
        • Feb 2008
        • 7142

        #4
        How many cells did you submit?

        Comment

        • CharlesG
          Junior Member
          • Jul 2019
          • 8

          #5
          Thanks a lot for helping. We submitted approximately 10000 (ten thousand cells) per condition (before and after treatment).

          Comment

          • GenoMax
            Senior Member
            • Feb 2008
            • 7142

            #6
            If we assume all 10000 cells survived. You want a minimum 50000 reads per cell so that is 500M reads * 2 conditions = 1 Billion clusters/single-end reads total. Sequencing length if fixed based on the kit used so you should just worry about reads than basepairs.

            According to 10x this will give you 30-50% saturation. If you need more saturation then you will need to sequence more. This assumes that libraries work/sequence well.
            Last edited by GenoMax; 04-20-2020, 12:18 PM.

            Comment

            • CharlesG
              Junior Member
              • Jul 2019
              • 8

              #7
              Thank you very much.

              Comment

              Latest Articles

              Collapse

              • SEQadmin2
                Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
                by SEQadmin2



                Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

                Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
                ...
                10-14-2026, 09:55 AM
              • SEQadmin2
                New Genomics Technologies Take Aim at Long-Standing Limits
                by SEQadmin2


                Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

                We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
                ...
                09-28-2026, 10:25 AM

              ad_right_rmr

              Collapse

              News

              Collapse

              Topics Statistics Last Post
              Started by SEQadmin2, 10-22-2026, 11:13 AM
              0 responses
              26 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-22-2026, 10:48 AM
              0 responses
              20 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-15-2026, 10:52 AM
              0 responses
              36 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-14-2026, 05:39 AM
              0 responses
              43 views
              0 reactions
              Last Post SEQadmin2  
              Working...