Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • How can I get the report by using SMRT command-line version?

    Now I have RS_IsoSeq command-line installed, and it works well for filter(getting reads of insert) classify(Getting full length reads) ,Isoform level clustering (ICE and Quiver),but how can I get the similar analysis report generated by SMRT Portal version with both statstic information and plot?

    In addition, how can I evaluate the quality of my rawdata(Quality Control)? Something like whether the data volume is enough(full passes?SMWs?),the quality of each reads(reads of insert accuracy?Q30?cluster reads accuracy?). Is there any software or script can do this?

    Thanks,
    huan
    happy

  • #2
    To generate the summary plot "fulllength_nonchimeric_readlength_hist.png", you will need to run the script "isoseq_classify_report.py", such as
    Code:
    mkdir -p report  && \
    isoseq_classify_report.py \
        isoseq_flnc.fasta  # output from pbtranscript.py classify
        isoseq.classify_summary.txt  # output from pbtranscript.py classify, it also contains the summary information
        output.json  # output json
        -o report  # output folder, need to exist

    Comment


    • #3
      @bowhan Thanks very much! It helps a lotO(∩_∩)O~
      happy

      Comment


      • #4
        Originally posted by huan View Post

        In addition, how can I evaluate the quality of my rawdata(Quality Control)? Something like whether the data volume is enough(full passes?SMWs?),the quality of each reads(reads of insert accuracy?Q30?cluster reads accuracy?). Is there any software or script can do this?

        Thanks,
        huan
        Hi, how do you solve this problem? Could you provide some advice or a link?Thanks!

        Comment


        • #5
          Hi,

          The simplest thing may be to run "RS_subreads" protocol in SMRTPortal. It gives you:

          # of P1 ZMWs in the "Loading" tab
          Polymerase (raw) read quality in the "Filtering" tab
          Mean subread length and total subread base in the "Subread filtering" tab

          You can also download the filtered subreads as a fasta file. That will give you further information about each subread and since the subread sequence IDs tell you which ZMW it is from (each ZMW can generate 0, 1, or more subreads), it gives you a sense of how many passes you are getting per ZMW.

          Hope this helps.

          --Liz

          Comment

          Latest Articles

          Collapse

          • seqadmin
            Recent Advances in Sequencing Analysis Tools
            by seqadmin


            The sequencing world is rapidly changing due to declining costs, enhanced accuracies, and the advent of newer, cutting-edge instruments. Equally important to these developments are improvements in sequencing analysis, a process that converts vast amounts of raw data into a comprehensible and meaningful form. This complex task requires expertise and the right analysis tools. In this article, we highlight the progress and innovation in sequencing analysis by reviewing several of the...
            Today, 07:48 AM
          • 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

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by seqadmin, Today, 07:17 AM
          0 responses
          11 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 05-02-2024, 08:06 AM
          0 responses
          19 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-30-2024, 12:17 PM
          0 responses
          20 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-29-2024, 10:49 AM
          0 responses
          28 views
          0 likes
          Last Post seqadmin  
          Working...
          X