Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Intersecting multiple bed files

    Hello,

    I have several RNA-Seq transcript data sets assembled and in BED format. I have masked out previously identified transcripts from the data, leaving me with "unidentified" transcripts. A visual of this data in the UCSC Genome Browser is attached.

    I need to computationally gather the locations where all of the resulting transcripts intersect. In looking though the bedtools intersect function, it seems that there is no option to specify regions where ALL the files intersect, only those where at least 2 of the supplied files intersect.

    Have any of you encountered this issue before? What are your suggested workarounds? Would I need to continually compare 2 files and then keep comparing that output to the next file and so on? Or is there an option I am unaware of/another software function that can handle this?

    Thank you all very much!
    -Anna
    Attached Files

  • #2
    bedops --intersect first.bed second.bed third.bed > result.bed

    Comment


    • #3
      Perfect, thanks!

      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...
        Yesterday, 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
      39 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
      55 views
      0 likes
      Last Post seqadmin  
      Working...
      X