Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Re. De Novo Assembly for RNA seq Data using Trinity

    Hi Everyone,

    I am trying to run De Novo Assembly for (Schizosaccharomyces pombe) and follow the steps described by (Haas., et al paper). In the methods section, they used Trinity software in order to do the De Novo Assembly and I'm just trying to reproduce what they did in the paper.

    I'm using the school server which has Trinity to do this but I wasn't able to unpack the file that has the RNA fq sequences reads when I used this command:
    tar –xvf TrinityNatureProtocolTutorial.tgz

    Also using Terminal linux commands in my Mac, how can I add RNA seq data to a new directory and view the right and left fq reads to be able to Run Trinity.

    Sorry, I am new to this.

    Thank you so much in advance.

  • #2
    Hi Hamad,

    to uncompress tgz files you should use:

    tar –xzvf TrinityNatureProtocolTutorial.tgz -C new_dir

    -z to use gnuzip
    -C to specify the directory where the extracted files will be placed

    Good luck!

    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
    36 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