Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • anyone1985
    Member
    • Mar 2009
    • 68

    MUMmer VS blastp

    I just finish a bacteria genome, then compare two genomes of the same genus. I hesitate between the MUMmer and blastp. Please give me some suggestions. And also, is there any software to get a dot plot from the result of blastp?
  • bio-x
    Member
    • Nov 2008
    • 18

    #2
    yes, you can try BSR, it is based on blastp.

    good luck!

    Comment

    • anyone1985
      Member
      • Mar 2009
      • 68

      #3
      Thank you for bio-x's kind help. I think accurately I'd like to get a dot plot of two genomes's ortholog plot by reciprocal best-hit pair from the result of pair-wise BLASTP. I guess there must be some software which is suitable to do this. Please give me some suggestions.

      Comment

      • Torst
        Senior Member
        • Apr 2008
        • 275

        #4
        Originally posted by anyone1985 View Post
        I think accurately I'd like to get a dot plot of two genomes's ortholog plot by reciprocal best-hit pair from the result of pair-wise BLASTP.
        "promer" from the Mummer suite will effectively do want you want. Although it doesn't examine "genes" it matches translated regions, which if there is a good match, are likely to be orthologs (or paralogs) anyway.

        Comment

        • anyone1985
          Member
          • Mar 2009
          • 68

          #5
          Yes, promer is pretty good. However, I'd like to draw the graph exactly. The promer can not give a clear position to identify the gene. Many literatures have figures as below. I am intrested in which software can draw such figure.

          Originally posted by Torst View Post
          "promer" from the Mummer suite will effectively do want you want. Although it doesn't examine "genes" it matches translated regions, which if there is a good match, are likely to be orthologs (or paralogs) anyway.
          Attached Files

          Comment

          • rahul.m.dhodapkar
            Member
            • Jun 2010
            • 28

            #6
            does anyone know how to fix the following MUMmer error?

            where textlen is the same as the length of build36 (hg18)

            ./mummer: suffix tree construction failed: textlen=3080436075 larger than maximal textlen=536870908

            Comment

            • robs
              Senior Member
              • May 2010
              • 116

              #7
              Try:


              The corresponding paper can be found here:

              Comment

              • rahul.m.dhodapkar
                Member
                • Jun 2010
                • 28

                #8
                @robs

                thanks, but the link says:

                [Thanks for the hint about the recent "MEMs" implementation that "can serve as a drop-in replacement for the MEMs algorithm in MUMmer 3". Seems to be working perfectly where MUMmer crashed :-) --Dan 15:08, 5 January 2010 (UTC)]

                what was the original hint? (sorry for any stupidity)

                Comment

                • robs
                  Senior Member
                  • May 2010
                  • 116

                  #9
                  Not sure what you mean with "original hint". There is only one hint and if you take a look at the paper you will see that the quote is actually from there.
                  The MEMs implementation has a mummer module that can be used instead of the MUMmer3 one. By doing this, mummer shouldn't crash anymore. More details are in the paper.

                  Comment

                  • rahul.m.dhodapkar
                    Member
                    • Jun 2010
                    • 28

                    #10
                    @robs

                    thanks so much for your help.

                    Comment

                    • Will Nelson
                      Member
                      • Nov 2010
                      • 16

                      #11
                      To solve the textlen problem, build a 64-bit version, and make sure
                      #define SIXTYFOURBITS is set in types.h.
                      (Grep for the one place this is used, to see where to set it).

                      Comment

                      • flxlex
                        Moderator
                        • Nov 2008
                        • 412

                        #12
                        Originally posted by Will Nelson View Post
                        To solve the textlen problem, build a 64-bit version, and make sure
                        #define SIXTYFOURBITS is set in types.h.
                        (Grep for the one place this is used, to see where to set it).
                        First, thanks for, as far as I can tell, the only solution to the mummer textlen problem on the web...

                        Not being an hardcore programmer, but a biologist-come-bioinformatician (more like a user of programs), it took me some time to figure out how to implement it, though. What you meant was to add this line

                        Code:
                        #define SIXTYFOURBITS
                        to the src/kurtz/libbasedir/types.h file before the line where it says

                        Code:
                        #ifdef SIXTYFOURBITS
                        and then run

                        Code:
                        make install
                        again.

                        (I had begun to 'uncomment' the ifdef line, causing all kinds of errors - like I said, not a programmer)

                        Just clarifying for future generations...

                        Comment

                        • colindaven
                          Senior Member
                          • Oct 2008
                          • 417

                          #13
                          This thread also supplies another solution:



                          "
                          If you recompile the package like so:

                          > make clean
                          > make CPPFLAGS="-O3 -DSIXTYFOURBITS"

                          you should have no more problems with space limitations.

                          Best,
                          -Adam
                          "

                          Comment

                          • cindy0805
                            Junior Member
                            • Jan 2013
                            • 1

                            #14
                            I want to compare to genomes with 87%similarity, I cant decide should I use Promer or NUCMER?

                            Comment

                            Latest Articles

                            Collapse

                            • mylaser
                              Reply to Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
                              by mylaser
                              Kheloyar – Everything You Need to Know About Kheloyaar Login and Kheoyar Id
                              If you are looking for an online gaming platform that offers a user-friendly experience, Kheloyar has become a name that many users search for. Whether you're interested in creating a new account, accessing your dashboard through Kheloyaar Login, or learning how to obtain a Kheoyar Id, understanding the platform's features and account process is essential.
                              This guide explains everything you need to know about...
                              Today, 01:13 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
                            • 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...
                              07-08-2026, 05:17 AM

                            ad_right_rmr

                            Collapse

                            News

                            Collapse

                            Topics Statistics Last Post
                            Started by SEQadmin2, 07-09-2026, 10:04 AM
                            0 responses
                            17 views
                            0 reactions
                            Last Post SEQadmin2  
                            Started by SEQadmin2, 07-08-2026, 10:08 AM
                            0 responses
                            10 views
                            0 reactions
                            Last Post SEQadmin2  
                            Started by SEQadmin2, 07-07-2026, 11:05 AM
                            0 responses
                            22 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...