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  • genbio
    Junior Member
    • Dec 2009
    • 1

    #1

    help with FLX 454

    Hi Everybody,

    I need help with FLX454. I want to get random sequences from a plant genome where no genomic data available. I would like to use these random sequences later in SSR identification which would be later my tools in phylogenetic studies. I've just started to learn about these next-generation sequencing.

    My questions could be so basic about the system and the methodology of shotgun sequencing. I thought about making shotgun sequencing in FLX, but I don't have a budget enough to sequence the whole genome. So how can I use shotgun sequencing for partial sequencing of this plants genome? Should I somehow try to specify my DNA pool for sequencing ? If so how can I make this?
    Could someone help me? I urgently need understand the system so please help me , thanks a lot!
  • flxlex
    Moderator
    • Nov 2008
    • 412

    #2
    Hi,

    Since you know nothing about your genome, you won't be able to to some sort of reduction straight away. Normally, I would have said use mRNA/cDNA sequencing to reduce the amount of sequence, bu I guess that won't work for SSRs.

    There are people out there who use AFLPs and sequence the bands, but with varying success...

    Good luck,

    flxlex

    Good luck,

    Comment

    • AKroxy
      Member
      • May 2009
      • 20

      #3
      To isolate microsatellites (SSRs), I think you could make magnetic beads (dynabeads) with a particular microsat sequence attached (ATATATATATAT for instance). Chop up the DNA, and isolate the DNA ATATATATAT containing DNA (and surrounding regions) with the dynabeads. You could do that for a bunch of different microsat sequences. Then you could pool all of the isolated DNA and 454 sequence it. Might be cheaper to clone and Sanger sequence though, unless you need a lot of loci. I think this is a pretty standard approach to SSR isolation.
      But if you are heading into the world of nextgen sequencing, perhaps there is a next gen approach to your phylogenetic question that would save time and money and get you way more data. Why go back to old-fashioned SSRs?

      Comment

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