Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • steven
    Senior Member
    • Aug 2009
    • 269

    #16
    Originally posted by NextGenSeq View Post
    You have to annotate your reference genome to know where the coding exons and SNPs are. After the assembly and SNP/DIP detection the software tells you if the variations are coding or known SNPs. You have to know this for mutation discovery.
    OK, so that is not "gene prediction" as mentioned in the first post -if i get it right. If you want to automatically annotated gene structures on a genomic sequence, then look for something like G-Morse or Cufflink, or a traditional gene finder.

    Comment

    • bioinfosm
      Senior Member
      • Jan 2008
      • 483

      #17
      sorry, but whats DIP?
      --
      bioinfosm

      Comment

      • steven
        Senior Member
        • Aug 2009
        • 269

        #18
        i bet on deletion insertion polymorphism.

        Comment

        • pedrotanno
          Junior Member
          • Oct 2009
          • 3

          #19
          Originally posted by NextGenSeq View Post
          CLC Bio is a bit buggy. You have to force import your reference genome as normal sequence data NOT next gen sequence data. Once you do that it is easy to annotate it using a GFF file. I tried attach the pdf describing it but this website gave an error message. If you private message me with your email address I can email it to you.

          Hi guys,
          I'm having the same problem using CLC ... and I couldn't find any viable solution...About this pdf... is it from Clc? Because not even using their example data from the 'Annotation Plug-in' we could make it work.

          Comment

          • zee
            NGS specialist
            • Apr 2008
            • 249

            #20
            If you're looking to do basic analysis have a look at some open solutions e.g. DIYA. It's quite simple to run a set of programs in serial. The hard part with annotation is manual curation and Artemis is a good tried and tested option. Geneious has some good offerings and it is prettier.

            Comment

            • pedrotanno
              Junior Member
              • Oct 2009
              • 3

              #21
              We are trying to know where the coding exons and SNPs are, to see if our snps are on coding regions.
              We tried to import one annotated reference genome and only the annotation file (GFF) but none of this approaches worked.

              Comment

              • NextGenSeq
                Senior Member
                • Apr 2009
                • 482

                #22
                Note CLC Bio will import the reference genome file from GenBank with the annotations. The files get very large if you include all the annotations. However, for small genomes it can handle all the annotations.

                Comment

                • pedrotanno
                  Junior Member
                  • Oct 2009
                  • 3

                  #23
                  Using Arthemis we can import the annotations, but using CLC and the same GFF annotation file we can't.
                  The problem using Artemis is that we are having problem extracting the snps annotations in CLC... so in one program we have the exon annotations and in CLC we have our snps annotations.

                  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, Today, 07:41 AM
                  0 responses
                  9 views
                  0 reactions
                  Last Post SEQadmin2  
                  Started by SEQadmin2, 08-03-2026, 10:13 AM
                  0 responses
                  25 views
                  0 reactions
                  Last Post SEQadmin2  
                  Started by SEQadmin2, 07-31-2026, 02:55 AM
                  0 responses
                  38 views
                  0 reactions
                  Last Post SEQadmin2  
                  Started by SEQadmin2, 07-24-2026, 12:17 PM
                  0 responses
                  25 views
                  0 reactions
                  Last Post SEQadmin2  
                  Working...