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  • woodydon
    Member
    • Jan 2010
    • 52

    #1

    Would RNA quality/quantity be good enough for sequencing when the liver tumor samples

    Dear all,

    Would RNA quality/quantity be good enough for sequencing when the liver tumor samples are frozen and sliced?

    One of my colleague thinks that the RNA quality should be fine for those cryo-sliced liver tumor samples. We just need to use more sliced samples to get enough RNA. Is this correct?

    One of my friends told me that the sliced liver tumor samples will have poor RNA quality, so I am worried. I am a totally dry lab geek. Could please someone help me? Thanks!

    Woody
    Last edited by woodydon; 04-02-2014, 09:59 PM.
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    The only way to find out would be to extract RNA from a bunch of slices and have a look on a bioanalyzer. I've sequenced RNA from frozen liver samples without issue, so unless the cryo-slicing wasn't really cryo enough then I would expect it'd work.

    Comment

    • woodydon
      Member
      • Jan 2010
      • 52

      #3
      Originally posted by dpryan View Post
      The only way to find out would be to extract RNA from a bunch of slices and have a look on a bioanalyzer. I've sequenced RNA from frozen liver samples without issue, so unless the cryo-slicing wasn't really cryo enough then I would expect it'd work.
      Hi dpryan,

      Thanks!

      Woody

      Comment

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