Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • rahul.m.dhodapkar
    Member
    • Jun 2010
    • 28

    #1

    MosaikJump not working properly

    Hello all,

    I have been trying to create a mosaik jump database from a reference fasta file (hg18, NCBI build 36). I'm using the following command:

    Code:
    ./MosaikJump -ia hg18_combined.dat -out hg18_combined.jmp -hs 15
    it starts off running fine, but when it gets to 5% completed, the ETA starts climbing and the "number of hashes" also starts climbing rapidly. this goes until both values roll over to 0, and then the program freezes. help much appreciated.

    -Rahul Dhodapkar
  • KevinLam
    Senior Member
    • Nov 2009
    • 204

    #2
    how much ram do you have?

    Code:
    MosaikJump -ia human_g1k_v37_chr_ucsc.fasta.dat -out human_g1k_v37_chr_ucsc.fasta_15 -hs 15 -mem 6
    works fine for me but I ran into memory problems again when I tried to aligned.
    http://kevin-gattaca.blogspot.com/

    Comment

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

      #3
      i have 10 GB of ram, is that insufficient for this task?

      -Rahul Dhodapkar
      Last edited by rahul.m.dhodapkar; 08-05-2010, 11:54 AM.

      Comment

      • tinacai
        Member
        • Apr 2010
        • 18

        #4
        Hello all,

        I have been trying to create a mosaikbuild vertion from a reference fasta file (hg18, NCBI build 36). I'm using the following command:
        ./Mosaikbuild -fr hg18.fa -oa hg18.dat ,warning
        ERROR: Could not open FASTA file (/home/database/hg18/hg18.fa) when performing integrity check
        but I input ./Mosaikbuild -fr chr1.fa -oa chr1.dat ,It can running now .my RAM is 32G,I want to kown if my RAM is low

        Comment

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

          #5
          32 Gigabytes of RAM should be plenty to convert hg18.fa to hg18.dat

          Comment

          • tinacai
            Member
            • Apr 2010
            • 18

            #6
            mosaik-aligner/bin/MosaikBuild -fr /home/database/hg18/hg18.fa.gz -oa /home/share2/chenchong/hg18.dat
            ------------------------------------------------------------------------------
            MosaikBuild 1.0.1388 2010-02-01
            Michael Stromberg Marth Lab, Boston College Biology Department
            ------------------------------------------------------------------------------

            - converting /home/database/hg18/hg18.fa.gz to a reference sequence archive.

            - parsing reference sequences:
            ref seqs: 49 (0.1205 ref seqs/s)

            - writing reference sequences:
            100%[==================================] 1.71 ref seqs/s in 28 s

            - calculating MD5 checksums:
            100%[==================================] 3.90 ref seqs/s in 12 s

            - writing reference sequence index:
            100%[==================================] 49.0 ref seqs/s in 1 s
            ERROR: Unable to allocate enough memory (3087005219 bytes) to create the concatenated reference sequence.
            my RAM is 32G,but the result warning Unable to allocate enough memory (3087005219 bytes) to create the concatenated reference sequence.

            Comment

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

              #7
              wait, why do you have 49 ref seqs? Shouldn't there only be 25 (22 autosomes + X, Y, M)? That might be the source of the problem. What exactly is in your hg18.fa file?

              Comment

              • tinacai
                Member
                • Apr 2010
                • 18

                #8
                >chr10
                >chr10_random
                >chr11
                >chr11_random
                >chr12
                >chr13
                >chr13_random
                >chr14
                >chr15
                >chr15_random
                >chr16
                >chr16_random
                >chr17
                >chr17_random
                >chr18
                >chr18_random
                >chr19
                >chr19_random
                >chr1
                >chr1_random
                >chr20
                >chr21
                >chr21_random
                >chr22
                >chr22_h2_hap1
                >chr22_random
                >chr2
                >chr2_random
                >chr3
                >chr3_random
                >chr4
                >chr4_random
                >chr5
                >chr5_h2_hap1
                >chr5_random
                >chr6_cox_hap1
                >chr6
                >chr6_qbl_hap2
                >chr6_random
                >chr7
                >chr7_random
                >chr8
                >chr8_random
                >chr9
                >chr9_random
                >chrM
                >chrX
                >chrX_random
                >chrY

                Comment

                • tinacai
                  Member
                  • Apr 2010
                  • 18

                  #9
                  this mine hg18.fa

                  Comment

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

                    #10
                    I'm not sure how useful anything that aligns to _random will be, since the _random .fa files contain random sequence that is on those chromosomes. They're bits that haven't been fitted in yet, so I would try removing those, and running MosaikBuild again and seeing where that puts you. It may well be that those additional sequences are eating up an enormous amount of memory. Let me know how that goes.

                    -Rahul Dhodapkar

                    Comment

                    • tinacai
                      Member
                      • Apr 2010
                      • 18

                      #11
                      [chenchong@node03 chenchong]$ mosaik-aligner/bin/MosaikBuild -fr /home/share2/chenchong/hg18/hg18.fa -oa /home/share2/chenchong/hg18.dat
                      ------------------------------------------------------------------------------
                      MosaikBuild 1.0.1388 2010-02-01
                      Michael Stromberg Marth Lab, Boston College Biology Department
                      ------------------------------------------------------------------------------

                      - converting /home/share2/chenchong/hg18/hg18.fa to a reference sequence archive.

                      - parsing reference sequences:
                      ref seqs: 25 (0.1938 ref seqs/s)

                      - writing reference sequences:
                      100%[==================================] 0.8736 ref seqs/s in 28 s

                      - calculating MD5 checksums:
                      100%[==================================] 1.99 ref seqs/s in 12 s

                      - writing reference sequence index:
                      100%[==================================] 25.0 ref seqs/s in 1 s
                      ERROR: Unable to allocate enough memory (3080448052 bytes) to create the concatenated reference sequence.
                      I have been removed the _random ,but the resullt seem to similar

                      Comment

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

                        #12
                        tinacai,

                        do you have a portal you can use to monitor the memory usage of your node? How much memory is the process using when it fails? Is there a memory usage spike?

                        -Rahul Dhodapkar

                        Comment

                        • tinacai
                          Member
                          • Apr 2010
                          • 18

                          #13
                          Rahul
                          I'm sure it is not problem for my memory, my RAM is 32G and only me is using it

                          Comment

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

                            #14
                            it's possible is that there is some sort of internal memory ceiling that prevents your process from using all of the RAM that you physically have available, which is why I'm asking if the memory usage is highest at the last step of the process

                            Comment

                            • tinacai
                              Member
                              • Apr 2010
                              • 18

                              #15
                              hi,Rahul
                              I have run my program again and check my memory situation,I found my memory usage highest at the last step of the process is 9.5%

                              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, 08-06-2026, 07:41 AM
                              0 responses
                              13 views
                              0 reactions
                              Last Post SEQadmin2  
                              Started by SEQadmin2, 08-03-2026, 10:13 AM
                              0 responses
                              30 views
                              0 reactions
                              Last Post SEQadmin2  
                              Started by SEQadmin2, 07-31-2026, 02:55 AM
                              0 responses
                              40 views
                              0 reactions
                              Last Post SEQadmin2  
                              Started by SEQadmin2, 07-24-2026, 12:17 PM
                              0 responses
                              26 views
                              0 reactions
                              Last Post SEQadmin2  
                              Working...