Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Patrick
    Member
    • Mar 2009
    • 27

    #1

    AMOS & BAMBUS program experience sharing and general user guide.

    Hi,

    Anybody willing to share the experience of using AMOS & BAMBUS program?
    Can give the general explanation about this two program and general user guide of these two program?
    Thanks a lot for sharing and advise
  • niazi84@hotmail.com
    Member
    • Jan 2010
    • 25

    #2
    HI Patrick,

    Did you get any assistance about AMOS. I am at the same position when you did this post. Any help you can do?
    ~Adnan~

    Comment

    • Patrick
      Member
      • Mar 2009
      • 27

      #3
      Hi,

      I just subscribe with the AMOS help. I learning from there now. What problem you have facing now? Anything I can help you too? Maybe we face the same situation too.

      Comment

      • niazi84@hotmail.com
        Member
        • Jan 2010
        • 25

        #4
        i have installed AMOS but i dont know how to make relevant input formats from illumina reads and reference sequence.
        ~Adnan~

        Comment

        • jjohnson
          Member
          • Aug 2009
          • 20

          #5
          Adnan,

          AMOS is a pretty large suite of tools, what are you trying to do more specifically, maybe I can share some war stories if I know where to start.
          Justin H. Johnson | Twitter: @BioInfo | LinkedIn: http://bit.ly/LIJHJ | EdgeBio

          Comment

          • niazi84@hotmail.com
            Member
            • Jan 2010
            • 25

            #6
            Thanks johnson. I am actually intending to do comparative assembly of bacterial strain whose data is from illumina GA2 with 75bp of reads. The data was in scarf format and i converted it into standard fastq format. Now the thing is that AMOScmp-shortreads takes two inputs .1con and .afg. How to convert reference sequence to .1con? And which steps should i follow till final assembly, viewing and validation? Thanks
            ~Adnan~

            Comment

            • niazi84@hotmail.com
              Member
              • Jan 2010
              • 25

              #7
              Also how i convert paired end reads in .afg format since nowhere on AMOS pages is mentioned about paired end reads conversion. I am gone mad in this, no help on the web and at AMOS-help.
              ~Adnan~

              Comment

              • Kasycas
                Member
                • Sep 2009
                • 22

                #8
                Hi [email protected],

                Did you find out about this reference file? I can't find much info anywhere about it!

                Thanks,

                Kasycas

                Comment

                • catfisher
                  Member
                  • Mar 2010
                  • 10

                  #9
                  I got an error when I make files for Bambus, can anybody give help? Thanks,
                  The error is bellow:

                  for i in src doc ;do cd $i ; make all; cd .. ; done
                  make[1]: Entering directory `/home/ngs/SL/software/bambus-2.33/src'
                  for i in IO DotLib TIGR_Foundation_CC grommit ;do cd $i ; make all; cd .. ; done
                  make[2]: Entering directory `/home/ngs/SL/software/bambus-2.33/src/IO'
                  make[2]: Nothing to be done for `all'.
                  make[2]: Leaving directory `/home/ngs/SL/software/bambus-2.33/src/IO'
                  make[2]: Entering directory `/home/ngs/SL/software/bambus-2.33/src/DotLib'
                  make[2]: Nothing to be done for `all'.
                  make[2]: Leaving directory `/home/ngs/SL/software/bambus-2.33/src/DotLib'
                  make[2]: Entering directory `/home/ngs/SL/software/bambus-2.33/src/TIGR_Foundation_CC'
                  g++ -D_HAS_GETOPT -c -o ConfigFile.o ConfigFile.cc
                  ConfigFile.cc: In member function ‘void ConfigFile:arseConfig()’:
                  ConfigFile.cc:113: error: ‘strlen’ was not declared in this scope
                  make[2]: *** [ConfigFile.o] Error 1
                  make[2]: Leaving directory `/home/ngs/SL/software/bambus-2.33/src/TIGR_Foundation_CC'
                  make[2]: Entering directory `/home/ngs/SL/software/bambus-2.33/src/grommit'
                  g++ -I../TIGR_Foundation_CC/ -g -c grommit.cc
                  grommit.cc: In function ‘int main(int, char**)’:
                  grommit.cc:236: warning: format ‘%s’ expects type ‘char*’, but argument 3 has type ‘char (*)[1024]’
                  grommit.cc:317: error: ‘abort’ was not declared in this scope
                  make[2]: *** [grommit.o] Error 1
                  make[2]: Leaving directory `/home/ngs/SL/software/bambus-2.33/src/grommit'
                  make[1]: Leaving directory `/home/ngs/SL/software/bambus-2.33/src'
                  make[1]: Entering directory `/home/ngs/SL/software/bambus-2.33/doc'
                  make[1]: Nothing to be done for `all'.
                  make[1]: Leaving directory `/home/ngs/SL/software/bambus-2.33/doc'

                  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, Yesterday, 11:13 AM
                  0 responses
                  16 views
                  0 reactions
                  Last Post SEQadmin2  
                  Started by SEQadmin2, Yesterday, 10:48 AM
                  0 responses
                  17 views
                  0 reactions
                  Last Post SEQadmin2  
                  Started by SEQadmin2, 10-15-2026, 10:52 AM
                  0 responses
                  35 views
                  0 reactions
                  Last Post SEQadmin2  
                  Started by SEQadmin2, 10-14-2026, 05:39 AM
                  0 responses
                  42 views
                  0 reactions
                  Last Post SEQadmin2  
                  Working...