Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • owlbike
    Junior Member
    • Feb 2019
    • 4

    #1

    De novo assembly

    hello everyone,

    I have recently started working in a lab and have been assigned the following task.

    AIM:To assemble the given sequences as one consensus for transformation to be even more specific. Looking for regions around trnA, trnI, 23s and 16s.

    Data I have:
    1) chloroplast genome sequence of an algae along with its circular map.

    2) Sequences of the Primers used. Three sets of primers have been used (forward and reverse) along with trnaI and trnaA (both forward and reverse).
    The sequences are in ".ab1" format.

    Please let me know how will you approach this problem.

    PS: No other files or data has been handed over to me. Its someone else's work and that person has left.
  • pmiguel
    Senior Member
    • Aug 2008
    • 2328

    #2
    Upon being given such a homework assignment, I would post it on appropriate web forums hoping to find someone gullible enough to save me from answering the question myself.

    Wait, no! I would not do that. But you did, didn't you?
    --
    Phillip

    Comment

    • owlbike
      Junior Member
      • Feb 2019
      • 4

      #3
      @pmiguel No, I didn't post any homework question. I framed it in a way (in points ) so that it becomes easier for everyone to understand and they can guide me. I have recently joined a lab and have been given someone's unfinished work with no complete data.

      Comment

      • pmiguel
        Senior Member
        • Aug 2008
        • 2328

        #4
        "You have recently started working in a lab and have been assigned the following task:"

        That was the first sentence of your homework question (or take home exam), right?

        --
        Phillip

        Comment

        • owlbike
          Junior Member
          • Feb 2019
          • 4

          #5
          yes that was the first line. Had to restate it because it seemed you missed it. If you can't help budding people in science you may not answer anything at all.

          Comment

          • skycreative
            Member
            • Jan 2010
            • 33

            #6
            convert the ab1 file to seq file, then you can try to assembly

            Comment

            Latest Articles

            Collapse

            • kinpict.com
              Reply to 16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
              by kinpict.com
              The part about this topic feels surprisingly grounded, and the details on the page is the bit that made me slow down. I’d keep <a href="https://kinpict.com/">ai family photo generator</a> bookmarked for later.
              Today, 06:37 PM
            • SEQadmin2
              16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
              by SEQadmin2





              NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification,...
              10-30-2026, 06:46 AM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by SEQadmin2, 11-12-2026, 07:59 AM
            0 responses
            25 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 11-05-2026, 09:25 AM
            0 responses
            35 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 11-03-2026, 11:54 AM
            2 responses
            53 views
            0 reactions
            Last Post kinpict.com  
            Started by SEQadmin2, 10-28-2026, 09:57 AM
            0 responses
            175 views
            0 reactions
            Last Post SEQadmin2  
            Working...