Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • dhanapala
    Junior Member
    • Nov 2011
    • 8

    #1

    50 bp Single end Vs 100 bp Single end Vs 50 bp Paired end

    Hi

    I have planned to do RNAseq in Soybean with 3 biological replicates

    May i know which type of sequencing would be the right one (Hi seq), if i would like to see the

    SNP difference
    Gene expression
    Differential expression and
    Splice junctions
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    For SNP calling you need to mark PCR duplicates. That works better with paired-end reads, so of the options I'd do 50bp paired-end. Paired-end reads will also be beneficial for mapping in general. You'll also be better able to differentiate isoforms with paired-end reads, if that's important to you.

    Comment

    • dhanapala
      Junior Member
      • Nov 2011
      • 8

      #3
      Thanks dpryan

      Since we have reference genome for Soybean

      So do you mean the 50bp PE is good option and still all above four analysis can be done ?

      How about the exon expression ? Is it possible too ?

      Comment

      • alexdobin
        Senior Member
        • Feb 2009
        • 161

        #4
        I would recommend doing 2x100bp

        Paired-end reads are preferred for de-convolution of isoform expression such as done by Cufflinks.
        On the other hand, longer reads allow for much more accurate detection of the splice junctions.

        Comment

        • adaptivegenome
          Super Moderator
          • Nov 2009
          • 436

          #5
          PE first priority, longer reads second. Any reason you can't do 100?

          Comment

          Latest Articles

          Collapse

          • SEQadmin2
            Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
            by SEQadmin2



            CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

            Despite this, “CRISPR helped turn genome editing from a specialized technique into
            ...
            07-31-2026, 11:01 AM
          • SEQadmin2
            Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
            by SEQadmin2


            Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

            The systematic characterization of the human proteome has
            ...
            07-20-2026, 11:48 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by SEQadmin2, 08-13-2026, 12:22 PM
          0 responses
          26 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 08-11-2026, 10:35 AM
          0 responses
          21 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 08-06-2026, 07:41 AM
          0 responses
          36 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 08-03-2026, 10:13 AM
          0 responses
          51 views
          0 reactions
          Last Post SEQadmin2  
          Working...