Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • TopNattapat
    Junior Member
    • Dec 2012
    • 2

    What does "non-redundant genomic sequence dataset" mean?

    Hello,

    I have read the paper "Identification of SNP and SSR markers in
    eggplant using RAD tag sequencing"



    and I don't understand the meaning of "non-redundant genomic
    sequence dataset" in abstract

    Could you help me, please?

    Thank you very much for your help
  • jimmybee
    Senior Member
    • Sep 2010
    • 119

    #2
    A non-redundant dataset is one where a single entry isn't repeated. For example, you are searching for something in a database and you find the same thing but in 2 different entries. That would mean there is redundancy within the dataset. A non-redundant database would be where there is only one entry

    Comment

    • maryam p
      Junior Member
      • Jul 2017
      • 5

      #3
      do you know about "custom-made perl script" in RNA Seq analysis? is it a software?

      Comment

      • GenoMax
        Senior Member
        • Feb 2008
        • 7142

        #4
        Originally posted by maryam p View Post
        do you know about "custom-made perl script" in RNA Seq analysis? is it a software?
        Not sure what reference this question is in but generally a perl script is a program written in Perl (a text processing programming language) for a specific purpose (custom part).

        Comment

        • Brian Bushnell
          Super Moderator
          • Jan 2014
          • 2709

          #5
          Originally posted by maryam p View Post
          do you know about "custom-made perl script" in RNA Seq analysis? is it a software?
          That seems to be completely unrelated to this thread. In such situations, I suggest you create a new post rather than adding to an old and irrelevant thread.

          Comment

          • maryam p
            Junior Member
            • Jul 2017
            • 5

            #6
            Thanks for your reply in a paper: https://www.ncbi.nlm.nih.gov/pmc/art...e.0129422.s001
            they have written:
            "GC counts of transcripts were determined using a custom-made perl script".
            I couldnt underestand diffinition of "custom-made perl script"
            many thanks

            Comment

            • ecgonina
              Junior Member
              • Aug 2018
              • 1

              #7
              "GC counts of transcripts were determined using a custom-made perl script".

              It means that indeed, they made a program that I guess takes each sequence, counst how many G and C's are and using a formula, calculates the percentage of GC in a whole sequence.

              Perl is a programming language.

              Comment

              Latest Articles

              Collapse

              • SEQadmin2
                Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
                by SEQadmin2



                Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
                ...
                Yesterday, 11:10 AM
              • SEQadmin2
                Cancer Drug Resistance: The Lingering Barrier to Rising Survival
                by SEQadmin2



                Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.

                There is no single reason why many patients don’t respond to treatment as expected. Cancer is...
                07-08-2026, 05:17 AM
              • GATTACAT
                Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
                by GATTACAT
                Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
                07-01-2026, 11:43 AM

              ad_right_rmr

              Collapse

              News

              Collapse

              Topics Statistics Last Post
              Started by SEQadmin2, Yesterday, 10:04 AM
              0 responses
              10 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 07-08-2026, 10:08 AM
              0 responses
              7 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 07-07-2026, 11:05 AM
              0 responses
              15 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 07-02-2026, 11:08 AM
              0 responses
              31 views
              0 reactions
              Last Post SEQadmin2  
              Working...