Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • ymc
    Senior Member
    • Mar 2010
    • 496

    #1

    Software to use Illumina reads for error correction?

    I am using Pilon. Seems ok to me.

    Are there better alternatives?

    I am using 2x250 MiSeq for error correction. Is there a better read length and machine-chemistry combo?
  • mido1951
    Senior Member
    • May 2014
    • 123

    #2
    you use the short reads from illumina to correct Nanopore long reads?

    Comment

    • ymc
      Senior Member
      • Mar 2010
      • 496

      #3
      Originally posted by mido1951 View Post
      you use the short reads from illumina to correct Nanopore long reads?
      Yeah, to be specific, I only try to correct the 2D reads

      Comment

      • mido1951
        Senior Member
        • May 2014
        • 123

        #4
        the NanoCorr for oxford nanopore reads correction.
        it is specific to the nanopore data.

        Comment

        • ymc
          Senior Member
          • Mar 2010
          • 496

          #5
          Thanks for your NanoCorr suggestion. Did you also try NaS? If so, how did it compare to NanoCorr? Its paper claims it can improve K12 genome to one mismatch per 100kbp.

          Comment

          • mido1951
            Senior Member
            • May 2014
            • 123

            #6
            Yes, I have used and tested NaS but I have not tested NanoCorr. I can not compare them because I have not tested NanoCorr. You have to see the results of the two papers, they used the same K12 genome.

            Comment

            • ymc
              Senior Member
              • Mar 2010
              • 496

              #7
              Originally posted by mido1951 View Post
              Yes, I have used and tested NaS but I have not tested NanoCorr. I can not compare them because I have not tested NanoCorr. You have to see the results of the two papers, they used the same K12 genome.
              Thank you very much for your reply.

              I am trying NaS now. It seems to output fasta of corrected nanopore reads. How do I feed fasta to celera assembler which is expecting a fastq?

              Comment

              • Dmitry.Antipov
                Junior Member
                • Feb 2013
                • 2

                #8
                I'm not sure that this is what you are interested in, but if you want to assemble Nanopore reads after error correction with Illumina, you can try SPAdes for hybrid assembly instead.

                Comment

                • mido1951
                  Senior Member
                  • May 2014
                  • 123

                  #9
                  do you have installed Nanocore?
                  I could not install it.

                  Comment

                  • ymc
                    Senior Member
                    • Mar 2010
                    • 496

                    #10
                    I could run both NaS and nanocorr to completion. But the resulting corrected fasta couldn't be assembled to a single contig whereas the uncorrected fasta could be assembled into one contig that is 94% identical to the reference E coli K12 MG1655 genome.

                    I used SRR1030394 from SRA to correct the 2d reads downloaded from

                    Comment

                    • mido1951
                      Senior Member
                      • May 2014
                      • 123

                      #11
                      for me, I could not install Nanocorr.
                      I do not know the problem.
                      do you have any problems during installation ??
                      Thank you

                      Comment

                      • ymc
                        Senior Member
                        • Mar 2010
                        • 496

                        #12
                        Originally posted by mido1951 View Post
                        for me, I could not install Nanocorr.
                        I do not know the problem.
                        do you have any problems during installation ??
                        Thank you
                        I don't have any problem. I just followed what was described in README.

                        Comment

                        • mido1951
                          Senior Member
                          • May 2014
                          • 123

                          #13
                          for NaS, I find not long reads corrected !!
                          NaS do long reads generated corrected? and where I find this file?
                          Thank you

                          Comment

                          • ymc
                            Senior Member
                            • Mar 2010
                            • 496

                            #14
                            Originally posted by mido1951 View Post
                            for NaS, I find not long reads corrected !!
                            NaS do long reads generated corrected? and where I find this file?
                            Thank you
                            NaS_hqctg_reads.fa?

                            Comment

                            Latest Articles

                            Collapse

                            • SEQadmin2
                              Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
                              by SEQadmin2



                              Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

                              Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
                              ...
                              10-14-2026, 09:55 AM
                            • SEQadmin2
                              New Genomics Technologies Take Aim at Long-Standing Limits
                              by SEQadmin2


                              Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

                              We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
                              ...
                              09-28-2026, 10:25 AM

                            ad_right_rmr

                            Collapse

                            News

                            Collapse

                            Topics Statistics Last Post
                            Started by SEQadmin2, 10-15-2026, 10:52 AM
                            0 responses
                            26 views
                            0 reactions
                            Last Post SEQadmin2  
                            Started by SEQadmin2, 10-14-2026, 05:39 AM
                            0 responses
                            32 views
                            0 reactions
                            Last Post SEQadmin2  
                            Started by SEQadmin2, 10-13-2026, 09:56 AM
                            0 responses
                            31 views
                            0 reactions
                            Last Post SEQadmin2  
                            Started by SEQadmin2, 10-09-2026, 11:14 AM
                            0 responses
                            28 views
                            0 reactions
                            Last Post SEQadmin2  
                            Working...