Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • mycorr10
    Junior Member
    • Dec 2011
    • 7

    #1

    Settings for cap3 assembly of cDNA to genomic data

    Hello,
    Sorry if there has been an answer to this elsewhere- i couldn't find it.
    I've been given the task of extending some short ESTs with pieces of genome sequence that have been accumulated for a particularly AT-rich organism. There is no complete genome yet but my lab doesn't want to wait for the assembly-which may be six months down the line.

    I've tried to align the ESTs to the genome contigs with cap3 but the assembly consistently fails to capture regions with introns properly.
    I have tried to alter the -f,-r, and -h parameters but it's my first time trying cap3 and haven't gotten it right.

    Can someone advise me about what are the correct parameters for this task?
    thank you.
  • aloliveira
    Member
    • Aug 2010
    • 47

    #2
    've tried to align the ESTs to the genome contigs with cap3 but the assembly consistently fails to capture regions with introns properly.I have tried to alter the -f,-r, and -h parameters but it's my first time trying cap3 and haven't gotten it right.
    Cap3 is an assembler program not an aligner program. If you want an alignment to the genome using EST use the program BLAT.

    Comment

    • mycorr10
      Junior Member
      • Dec 2011
      • 7

      #3
      I've already used blat to find the appropriate genome contigs that match the EST but it doesn't fit my needs. What i need is a program that does multiple sequence alignment capable of incorporating large gaps such as introns. BLAT does a good job of ID the right pieces but I'm trying to define the whole-length gene and therefore need a decent alignment program. CAP3 was the program suggested to me but if someone has a better suggestion I'd appreciate it.

      Comment

      • tbanks
        Member
        • Mar 2010
        • 11

        #4
        Exonerate is a great piece of software for sequence alignment. Check out the est2genome option.

        Comment

        • mycorr10
          Junior Member
          • Dec 2011
          • 7

          #5
          Yes,
          I like exonerate but since my genome isn't assembled i don't get a convenient multiple sequence alignment out of it. I often have two or three long genome contigs that align to my EST and the output of the program just gives a one to one cDNA to contig alignment. Again it may be a question of finding the right parameters cause I'm new to exonerate too but so far I haven't found a command line program that can do what a commercial MSA program like CodonCodeAligner or sequencher can do- which is a pity cause I'd love to automate this procedure...
          If I'm wrong about the capabilities of exonerate I'd love some clarification.

          Comment

          • pkerrwall
            Junior Member
            • Dec 2009
            • 2

            #6
            Did you find a solution to this problem? I need to do a similar job. Wish we knew the clustal options that the Sequencher Large Gap option uses.

            Comment

            • sphil
              Senior Member
              • Apr 2010
              • 192

              #7
              Hey,

              SSPACE is a tool which migrates cDNA (i.e. RNA-seq data) with standard DNA contigs. It uses PE as well as SE reads and gives you the chance to close gaps etc. using cDNA. Available at:

              Comment

              • mycorr10
                Junior Member
                • Dec 2011
                • 7

                #8
                Thanks I will check that out. A day or two ago someone suggested an alignment tool called Spicey and then they promptly left town. I can't find a reference or website for it but when they get back to me I'll post it.

                Comment

                • kmcarr
                  Senior Member
                  • May 2008
                  • 1181

                  #9
                  Originally posted by mycorr10 View Post
                  Thanks I will check that out. A day or two ago someone suggested an alignment tool called Spicey and then they promptly left town. I can't find a reference or website for it but when they get back to me I'll post it.
                  They probably meant 'Spidey'
                  Last edited by kmcarr; 01-16-2012, 07:40 AM. Reason: fix typo

                  Comment

                  • mycorr10
                    Junior Member
                    • Dec 2011
                    • 7

                    #10
                    Oh that does look likely - thanks.

                    Comment

                    • mycorr10
                      Junior Member
                      • Dec 2011
                      • 7

                      #11
                      getting a usable alignment out of exonerate

                      Though I posted a separate thread for this I've gotten no response there so I'm asking here. As of now I've found exonerate to be useful in aligning ests to genomic dna and the output is supposed to be easy to parse but I'm not that great at writing my own code. Does anyone have existing scripts they'd ve willing to share to parse and combine the alignments from exonerate to create a consensus sequence?

                      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
                      23 views
                      0 reactions
                      Last Post SEQadmin2  
                      Started by SEQadmin2, 10-14-2026, 05:39 AM
                      0 responses
                      28 views
                      0 reactions
                      Last Post SEQadmin2  
                      Started by SEQadmin2, 10-13-2026, 09:56 AM
                      0 responses
                      25 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...