Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • NGS_New_User
    Member
    • Sep 2012
    • 41

    #1

    Annotating and finding genes of a non-model organism (no reference genome)

    I desperately need some help in brainstorming how to approach my data. I have a de novo assembled genome of a non-model organism (no available reference genome) and my end goal is to annotate it and find the genes that determine/play a role in sex development. I plan to map/align the assembly to a related species that has an annotated reference genome. The data was sequenced pair end by illumina hiseq.
    I am stuck on what to do next, what would be a suggested pipeline on how to go about finding the genes of interest? And what programs/software open source or commercial can I use to achieve that? How do I go about annotating it?
    A related post I posted some few weeks ago is below, no responses yet
    Please, any ideas/suggestions or directions to an already similar answered post are welcomed.
    Thank you very much.

    Originally posted by NGS_New_User View Post
    Hello,

    I currently ran a de novo assembly on a male and female genome of a non-model organism.
    My plan is to compare the male and female genomes (get percentage of similarity and differences) then extract and annotate the sections that are unique between them.
    Additionally, I also plan to align(map) both male and female genomes with a well annotated genome of a related species (model organism); and annotate regions of similarities as well as finding out the percentage of how different or similar they are.

    My question is, what are the recommended ngs programs (soft ware) that I should use to accomplish what I want to do?

    Any suggestions will be appreciated
  • rhinoceros
    Senior Member
    • Apr 2013
    • 372

    #2
    Predict proteins with FragGeneScan. Blastp against nr. Predict tRNAs with tRNAscan-SE. Predict rRNAs with Blastn against silva SSU and LSURef?

    Alternatively, you could consider just submitting your data to IMG (if it's suitable for your organism) and let them do the computations for you? You could at least have a look at their SOP for ideas?
    Last edited by rhinoceros; 01-23-2014, 10:49 AM.
    savetherhino.org

    Comment

    • jimmybee
      Senior Member
      • Sep 2010
      • 119

      #3
      It completely depends on your species/sequence.

      How big is your genome? Is it repetitive? How close (taxonomically) is the nearest well-annotated genome? Have you outlined functional gene families that you want to target?

      Best bet is to identify ORFs with a gene finder (FGENESH, Augustus, GENSCAN), extract sequences and BLAST against a well-annotated gene/protein db of a closely related species...

      Comment

      • Joann
        Senior Member
        • Oct 2008
        • 230

        #4
        Originally posted by NGS_New_User View Post
        my end goal is to annotate it and find the genes that determine/play a role in sex development
        Thank you very much.
        Is this an organism possessing a phenotypic male and female organism in it's reproductive cycle or does it have a more obscure developmental strategy?

        Comment

        • NGS_New_User
          Member
          • Sep 2012
          • 41

          #5
          Originally posted by Joann View Post
          Is this an organism possessing a phenotypic male and female organism in it's reproductive cycle or does it have a more obscure developmental strategy?
          Yes, it has a phenotypic male and female in its reproductive cycle

          Comment

          • JackieBadger
            Senior Member
            • Mar 2009
            • 385

            #6
            Originally posted by jimmybee View Post
            It completely depends on your species/sequence.

            How big is your genome? Is it repetitive? How close (taxonomically) is the nearest well-annotated genome? Have you outlined functional gene families that you want to target?

            Best bet is to identify ORFs with a gene finder (FGENESH, Augustus, GENSCAN), extract sequences and BLAST against a well-annotated gene/protein db of a closely related species...
            Agreed.
            Find contigs with ORFs, and then run these through BLAST2GO. You can then filter the annotations based on E-value

            Comment

            • Anemone
              Junior Member
              • Sep 2012
              • 3

              #7
              Would like to just follow up on this post a little bit. Is it possible to get some faster annotation than by Blast2GO for non-model organisms? For me at least the blast step is running very slow (meaning weeks), even if using a more powerful computer. Does it help a lot to get a local BLAST database?? Or anyone has experience with the new Blast2GO CLC plugin, does it run faster? Thanks in advance!! :-)

              Comment

              • yueluo
                Member
                • Aug 2013
                • 82

                #8
                Originally posted by Anemone View Post
                Would like to just follow up on this post a little bit. Is it possible to get some faster annotation than by Blast2GO for non-model organisms? For me at least the blast step is running very slow (meaning weeks), even if using a more powerful computer. Does it help a lot to get a local BLAST database?? Or anyone has experience with the new Blast2GO CLC plugin, does it run faster? Thanks in advance!! :-)
                Setting up a local blast and blast2go database would certaining speed things up if you have access to a server/cluster.

                Comment

                Latest Articles

                Collapse

                • SEQadmin2
                  Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
                  by SEQadmin2



                  CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

                  Despite this, “CRISPR helped turn genome editing from a specialized technique into
                  ...
                  07-31-2026, 11:01 AM
                • SEQadmin2
                  Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
                  by SEQadmin2


                  Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

                  The systematic characterization of the human proteome has
                  ...
                  07-20-2026, 11:48 AM
                • 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.
                  ...
                  07-09-2026, 11:10 AM

                ad_right_rmr

                Collapse

                News

                Collapse

                Topics Statistics Last Post
                Started by SEQadmin2, 08-03-2026, 10:13 AM
                0 responses
                15 views
                0 reactions
                Last Post SEQadmin2  
                Started by SEQadmin2, 07-31-2026, 02:55 AM
                0 responses
                32 views
                0 reactions
                Last Post SEQadmin2  
                Started by SEQadmin2, 07-24-2026, 12:17 PM
                0 responses
                23 views
                0 reactions
                Last Post SEQadmin2  
                Started by SEQadmin2, 07-23-2026, 11:41 AM
                0 responses
                21 views
                0 reactions
                Last Post SEQadmin2  
                Working...