Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Is left end (_1.fq) of normally mapped reads always positive strand?

    Is it true?

    Thanks.

  • #2
    In a normal genomic paired end library there should be no preference for whether the first read of the pair maps to the original top or bottom strands. The only constraint should be that the second read should map to the opposite strand to the first and that the 3' ends of the two reads should point towards each other - usually separated by the approximate insert size of the library. If you are viewing these mapped pairs of reads in a genome browser then the read on the left (most 5' on the top strand) could have come from either the first or second read of the actual sequencing run.

    There are library preparation methods (mostly RNA-Seq or ChIP-Seq) where a single strand is selected, so the coverage of a region will be strand biased, but this won't be a global effect (ie everything on the same genomic strand), but will be localised to a specific transcript or binding site.

    Comment


    • #3
      Thank you

      It helps me a lot.

      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, Yesterday, 08:47 AM
      0 responses
      12 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
      59 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-10-2024, 09:21 AM
      0 responses
      54 views
      0 likes
      Last Post seqadmin  
      Working...
      X