Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • suludana
    Member
    • May 2008
    • 61

    #1

    Index

    Hi,
    someone had news about the launch of the indexing kit?

    Thanks
  • monad
    Member
    • May 2008
    • 40

    #2
    It is now officially available (see below).

    Multiplexing Sample Preparation
    Oligonucleotide Kit
    Kitted oligonucleotides used to prepare up to
    96 samples for multiplexed sequencing.
    PE-400-1001

    Multiplexing Sequencing Primers
    and PhiX Control Kit
    Kitted multiplexing sequencing primers, multiplexing
    control DNA, and buffer set. Sufficient for up to
    10 Genome Analyzer runs.
    PE-400-1002

    Comment

    • ShirleyHS
      Junior Member
      • Dec 2008
      • 5

      #3
      Hi,

      Has anyone tried the indexing? Any success? difficulties? Will be glad to receive insights as far as sample prep / sequencing / analysis are concerned.

      Shirley.

      Comment

      • floor121
        Junior Member
        • Feb 2008
        • 6

        #4
        I try to sample prep with the index kit last month, it seems work well and the workflow is almost the same as PE library prep except PCR, however, the index libraries cannot run with normal PE libraries, it is not easy to construct 7 libraries to run at the same time.
        Last edited by floor121; 08-16-2011, 10:41 AM.

        Comment

        • suludana
          Member
          • May 2008
          • 61

          #5
          I also see this problem.
          Moreover the kits of sample preparation do not adjust well (in number of samples) to the kits of index…

          Comment

          • ShirleyHS
            Junior Member
            • Dec 2008
            • 5

            #6
            Any experience with analyzing the indexed samples? Are they well-separated?

            Comment

            • scooterdog
              Junior Member
              • Sep 2008
              • 3

              #7
              I've heard that the cost for indexing is $30 more on a per-sample basis. So to index 12 samples on a single lane, is it a one-sample library prep cost (say $370 for doing a library prep on 12 samples) or is it 12 times the single-sample library prep ($370 x 12 = $4,440) just with the index?

              Comment

              • huguesparri
                Member
                • May 2008
                • 97

                #8
                The library generation cost is not reduced (it's a bit higher) as you have to go through the entire library preparation protocole. The indexing is taking place in the last PCR step.
                You earn money on the cluster and sequencing part: you only use 1 paired end cluster generation kit and 1 (+ part of another one to sequence the indexing tag) sequencing kit for up to 96 samples.

                Comment

                • scooterdog
                  Junior Member
                  • Sep 2008
                  • 3

                  #9
                  Thanks huguesparri for the reply.

                  So if I understand correctly then for 84 samples (12 x 7 lanes) the library preparation alone would be some 84 x $370 = $31,080 for the library preparation alone, and of course the per-sample cost for the cluster-generation/SBS is cut down by a factor of 84... a very expensive experiment...

                  Comment

                  • huguesparri
                    Member
                    • May 2008
                    • 97

                    #10
                    You can also try the "100 RXN Paired End Oligo Only Kit" (PE-102-1003).
                    Illumina's price is € 4.445,16 ( like 6000 US$ or so) for our department.
                    I didn't calculated if it's cheaper as it's depending on the price you have for the "non-Illumina's" supplies but it can be an option...

                    Comment

                    • bioinfosm
                      Senior Member
                      • Jan 2008
                      • 483

                      #11
                      Originally posted by ShirleyHS View Post
                      Any experience with analyzing the indexed samples? Are they well-separated?
                      Yes.. the samples are well separated. Although I would think some index would be closer to a few others, making it useful to group selective indexes in a lane if thats an option
                      --
                      bioinfosm

                      Comment

                      • Aaron Cooper
                        Member
                        • Feb 2011
                        • 15

                        #12
                        This question is in response to the above comment that index reads cannot be done mixed in with PE libraries without indexes.

                        I am planning on doing SE 100 sequencing, but for multiple reasons I'd like to use a PE adapter with an index. The sequencing core at our institution accepts lanes for sequencing and will batch your library with several others to fill a flow cell. Does anyone know if it is possible with regard to the GAIIx/HiSeq 2000 instruments and Illumina software to get an index read if not all of the lanes have PE adapters?

                        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
                        58 views
                        0 reactions
                        Last Post SEQadmin2  
                        Started by SEQadmin2, 10-22-2026, 10:48 AM
                        0 responses
                        42 views
                        0 reactions
                        Last Post SEQadmin2  
                        Started by SEQadmin2, 10-15-2026, 10:52 AM
                        0 responses
                        46 views
                        0 reactions
                        Last Post SEQadmin2  
                        Started by SEQadmin2, 10-14-2026, 05:39 AM
                        0 responses
                        48 views
                        0 reactions
                        Last Post SEQadmin2  
                        Working...