Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • Single-end sequencing for RNA-seq

    Hello everybody,

    we have to run some RNA-seq experiments on HiSeq 2500, and the sequencing facility has lots of experience with exomes/genomes resequencing, but very little experience with mRNA-seq. Overall, from what I know, the consensus is that for read count-based methods (ChIP-seq, RNA-seq) you want to run single-end sequencing with shorter read length, to get more individual reads from the same reagents.

    What are the pitfalls and recommendations to get the best throughput from a single-end experiment in terms of cluster density, concentrations, etc?

    Thank you in advance

  • #2
    Originally posted by apredeus View Post
    Hello everybody,

    we have to run some RNA-seq experiments on HiSeq 2500, and the sequencing facility has lots of experience with exomes/genomes resequencing, but very little experience with mRNA-seq. Overall, from what I know, the consensus is that for read count-based methods (ChIP-seq, RNA-seq) you want to run single-end sequencing with shorter read length, to get more individual reads from the same reagents.

    What are the pitfalls and recommendations to get the best throughput from a single-end experiment in terms of cluster density, concentrations, etc?

    Thank you in advance
    Performing a single end read will not "get more individual reads from the same reagents". The optimal cluster density (number of reads) obtained from one HiSeq 2500 flow cell lane is the same regardless of whether it is a single end or paired end read, DNA, RNA or ChIP-Seq library. Once the Illumina library is made it makes (virtually) no difference to the sequencer what the starting material was or the kit used to create the library. You load an mRNA library the same way you load a DNA library. The difference is you purchase a Single Read flow cell kit and a 50 cycle reagent kit to perform your run. That's what saves you money.

    Comment


    • #3
      Thank you very much! As I don't work with the sequencer itself directly, that's what was eluding me. I knew about the "less reagents" argument, but not about the different flow cell.

      Thanks again.

      Comment

      Latest Articles

      Collapse

      • seqadmin
        Essential Discoveries and Tools in Epitranscriptomics
        by seqadmin




        The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...
        04-22-2024, 07:01 AM
      • seqadmin
        Current Approaches to Protein Sequencing
        by seqadmin


        Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
        04-04-2024, 04:25 PM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by seqadmin, Today, 08:47 AM
      0 responses
      10 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-11-2024, 12:08 PM
      0 responses
      60 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-10-2024, 10:19 PM
      0 responses
      57 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-10-2024, 09:21 AM
      0 responses
      53 views
      0 likes
      Last Post seqadmin  
      Working...
      X