Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • how to define a forward or reverse read file

    i often meet the concept of "forward" or "reverse".
    but not exact definition provided

    does the "forward" means the reads who have the same direction with PCR primer 1 ?
    does the "reverse". means the reads who have the same direction with PCR primer 2 ?

    thank u very much
    shan gao

  • #2
    In relation to your sequence:
    Forward: 5' to 3'
    Reverse: 3' to 5'

    Comment


    • #3
      no, not that simple

      In classical biology, we define "Forward" is the direction from 5' to 3' and "Reverse". 3' to 5'. but in NGS sequencing, all the sequences direction is from 5' to 3' , so F means sense strand, and R means anti sense.but in classical biology, we define sense strand is mRNA direction. those concepts are a little confusing.

      and also in the Trinity algorithm, i think sense or antisense is just oppossite to each other. if you define one srtand is sense, the other one is antisense. trinity donot care which one is which one. i think you design this parameter --SS_lib_type, just to make the output sequences following
      the sense direction which defined by users.

      Comment


      • #4
        I would agree with Soleil...the way people use forward and reverse in NGS context, the forward read is the one that is in the same direction as your reference, and the reverse is the one that is in the opposite direction. Of course, what might be forward for a genone might be reverse when talking about a transcript.

        If you were doing something other than an ordinary genomic prep, like you were doing PCR, with the adaptors incorporated into the PCR primers, and putting that product onto the flow cell, then there would be a solid correlation between read 1 and the direction of the read itsself, with respect to the reference. But with ordinary genomic-type preps, the DNA gets sheared, and adaptors are ligated, and they don't know which way the DNA was oriented with respect to the telomere, or whether your reference puts the telomere at the start or the end of your refeence. So reads go in all directions. So really, all that matters is that for each cluster, read 1 runs one way, and read 2 runs the other way; towards each other in paired end, away from each other in mate-pair.

        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 on Modified Bases...
          Today, 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, 04-11-2024, 12:08 PM
        0 responses
        37 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-10-2024, 10:19 PM
        0 responses
        41 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-10-2024, 09:21 AM
        0 responses
        35 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-04-2024, 09:00 AM
        0 responses
        54 views
        0 likes
        Last Post seqadmin  
        Working...
        X