Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • yjpark1091
    Junior Member
    • May 2017
    • 4

    Genome assembly using Pacbio sequel data

    Hello guys~

    I got a fungal genome sequencing data using sequel platform.

    Also, I already finish to set up SMRT Link and SMRT analysis to lab server.

    The reason why I make new post in pacbio forum is getting an opinion about choosing assemble protocol (HGAP2, HGAP3, HAGP4 ....)

    Please tell or suggest me about best assemble protocol if there any guys that assemble fungal genome data from pacbio platform.

    Any opinion, source, or comments are okay.
    Thank you.
  • rhall
    Senior Member
    • Aug 2012
    • 324

    #2
    HGAP.4, it's actually not possible to run sequel data through the HGAP.2 and HGAP.3 pipelines.
    How big is the fungi? so long as you have reasonable coverage default parameters should be a good starting point.

    Comment

    • yjpark1091
      Junior Member
      • May 2017
      • 4

      #3
      I think it is almost 30 Mb and consist of several chromosome.
      The value is also just estimation. Also there is no sequencing report of fungal genome that similar with my fungal genome.
      And I already try to analyzed my fungal genome sequel data using HGAP.4 in Pacbio SMRT Link but the result is not good that sum of polish contig is not same with estimate genome size of my fungal genome.
      In this case, how can i improve my sequening result?

      Comment

      • GenoMax
        Senior Member
        • Feb 2008
        • 7142

        #4
        Post some of the stats from your HGAP.4 run. Dr. Hall will likely need those to comment further.

        Comment

        • rhall
          Senior Member
          • Aug 2012
          • 324

          #5
          Preassembled yield, polished contig total size and what the raw coverage of the polished contigs is would be a good place to start.

          Comment

          • SNPsaurus
            Registered Vendor
            • May 2013
            • 525

            #6
            You could look at completeness by running Busco on it. http://busco.ezlab.org/
            Providing nextRAD genotyping and PacBio sequencing services. http://snpsaurus.com

            Comment

            Latest Articles

            Collapse

            • SEQadmin2
              Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
              by SEQadmin2



              Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
              ...
              Today, 11:10 AM
            • SEQadmin2
              Cancer Drug Resistance: The Lingering Barrier to Rising Survival
              by SEQadmin2



              Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.

              There is no single reason why many patients don’t respond to treatment as expected. Cancer is...
              Yesterday, 05:17 AM
            • GATTACAT
              Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
              by GATTACAT
              Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
              07-01-2026, 11:43 AM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by SEQadmin2, Today, 10:04 AM
            0 responses
            8 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, Yesterday, 10:08 AM
            0 responses
            7 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-07-2026, 11:05 AM
            0 responses
            9 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-02-2026, 11:08 AM
            0 responses
            31 views
            0 reactions
            Last Post SEQadmin2  
            Working...