Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • El Crazy Xabi
    Junior Member
    • Aug 2014
    • 4

    #241
    For those with the problem with the -x 1 "Process 'extend/format contigs' failed":
    I wrote an email yesterday to the company that distributes the program (Baseclear) and they told me:
    I understand this point, yet we do not have plans at this very moment to address this.
    So please continue to use the –x 0 option. My apologies.
    So I asked for a previous version and they send me the 2.0.

    Good luck.

    PS: the 2.0 needs Perl 4 ¬¬'
    Last edited by El Crazy Xabi; 02-09-2016, 04:12 PM.

    Comment

    • milo0615
      Member
      • Dec 2012
      • 39

      #242
      Hello,

      Were you guys able to figure it out? I am running SSPACE x_64 with options (x=1 and T=16) but I am getting the following error:

      =>Mon Mar 7 15:46:00 2016: Extending of contigs with unmapped reads

      =>Mon Mar 7 15:46:00 2016: Building Bowtie index for contigs

      =>Mon Mar 7 16:58:09 2016: Mapping reads to contigs with Bowtie
      Thread 18 terminated abnormally: Can't open bwa output -- fatal
      **************************************************

      Process 'extend/format contigs' failed on Mon Mar 7 23:58:49 2016


      I would really appreciate your help.

      Comment

      • sunnycqcn
        Member
        • Apr 2013
        • 17

        #243
        Could you present your whole command?




        Originally posted by milo0615 View Post
        Hello,

        Were you guys able to figure it out? I am running SSPACE x_64 with options (x=1 and T=16) but I am getting the following error:

        =>Mon Mar 7 15:46:00 2016: Extending of contigs with unmapped reads

        =>Mon Mar 7 15:46:00 2016: Building Bowtie index for contigs

        =>Mon Mar 7 16:58:09 2016: Mapping reads to contigs with Bowtie
        Thread 18 terminated abnormally: Can't open bwa output -- fatal
        **************************************************

        Process 'extend/format contigs' failed on Mon Mar 7 23:58:49 2016


        I would really appreciate your help.

        Comment

        • milo0615
          Member
          • Dec 2012
          • 39

          #244
          Originally posted by sunnycqcn View Post
          Could you present your whole command?
          Hi sunnycqcn,

          The command I used is as follows. Thank you for your help

          >perl $HOME/SSPACE-STANDARD-3.0_linux-x86_64/SSPACE_Standard_v3.0.pl -l libraries.txt -s gercombsadaptrim200_k44-contigs.fa -x 1 -z 200 -T 16 -k 3 -a 0.7 -m 32 -r 0.9 -p 0 -o 15 -n 10 -v 1 -b gercombsk44 &

          [1] 20196

          log:

          [stilllab@b30-fac-staff-134-71-20-58 NEW_SSPACE_Gerreg]$ Your inserted inputs on [SSPACE_Standard_v3.0_linux] at Mon Mar 7 15:40:17 2016:
          Required inputs:
          -l = libraries.txt
          Number of paired files = 2
          -s = gercombsadaptrim200_k44-contigs.fa
          -b = gercombsk44

          Optional inputs:
          -x = 1
          -z = 200
          -k = 3
          -g = 0
          -a = 0.7
          -n = 10
          -T = 16
          -p = 0

          Contig extension inputs:
          -o = 15
          -m = 32
          -r = 0.9


          =>Mon Mar 7 15:40:17 2016: Reading, filtering and converting input sequences of library file initiated

          ------------------------------------------------------------

          =>Mon Mar 7 15:46:00 2016: Extending of contigs with unmapped reads

          =>Mon Mar 7 15:46:00 2016: Building Bowtie index for contigs

          =>Mon Mar 7 16:58:09 2016: Mapping reads to contigs with Bowtie
          Thread 18 terminated abnormally: Can't open bwa output -- fatal
          **************************************************

          Process 'extend/format contigs' failed on Mon Mar 7 23:58:49 2016

          Comment

          • fahmida
            Member
            • Aug 2010
            • 54

            #245
            Originally posted by milo0615 View Post
            Hi sunnycqcn,

            The command I used is as follows. Thank you for your help

            >perl $HOME/SSPACE-STANDARD-3.0_linux-x86_64/SSPACE_Standard_v3.0.pl -l libraries.txt -s gercombsadaptrim200_k44-contigs.fa -x 1 -z 200 -T 16 -k 3 -a 0.7 -m 32 -r 0.9 -p 0 -o 15 -n 10 -v 1 -b gercombsk44 &

            [1] 20196

            log:

            [stilllab@b30-fac-staff-134-71-20-58 NEW_SSPACE_Gerreg]$ Your inserted inputs on [SSPACE_Standard_v3.0_linux] at Mon Mar 7 15:40:17 2016:
            Required inputs:
            -l = libraries.txt
            Number of paired files = 2
            -s = gercombsadaptrim200_k44-contigs.fa
            -b = gercombsk44

            Optional inputs:
            -x = 1
            -z = 200
            -k = 3
            -g = 0
            -a = 0.7
            -n = 10
            -T = 16
            -p = 0

            Contig extension inputs:
            -o = 15
            -m = 32
            -r = 0.9


            =>Mon Mar 7 15:40:17 2016: Reading, filtering and converting input sequences of library file initiated

            ------------------------------------------------------------

            =>Mon Mar 7 15:46:00 2016: Extending of contigs with unmapped reads

            =>Mon Mar 7 15:46:00 2016: Building Bowtie index for contigs

            =>Mon Mar 7 16:58:09 2016: Mapping reads to contigs with Bowtie
            Thread 18 terminated abnormally: Can't open bwa output -- fatal
            **************************************************

            Process 'extend/format contigs' failed on Mon Mar 7 23:58:49 2016
            Please see the response of 'El Crazy Xabi' above.
            Either use -x = 0 or use an older version of SSPACE.

            Comment

            • milo0615
              Member
              • Dec 2012
              • 39

              #246
              Originally posted by fahmida View Post
              Please see the response of 'El Crazy Xabi' above.
              Either use -x = 0 or use an older version of SSPACE.
              Hi fahmida,

              If I use -x = 0 the assembly stats such as the N50, n>200, and max length stay the same. I have already emailed the SSPACE developers for an older version of it.

              Thank you for your help.

              -Milo

              Comment

              • sunnycqcn
                Member
                • Apr 2013
                • 17

                #247
                I am sure the 3.0 version work well with the big genome. I assembled one genome last month, it worked well. Meanwhile, I met the same problem as same with you. So if your library file include a lot of libraries, the error file should be like as your error file. So if you can present your library file, I can know what it happen.



                Originally posted by milo0615 View Post
                Hi fahmida,

                If I use -x = 0 the assembly stats such as the N50, n>200, and max length stay the same. I have already emailed the SSPACE developers for an older version of it.

                Thank you for your help.

                -Milo

                Comment

                • El Crazy Xabi
                  Junior Member
                  • Aug 2014
                  • 4

                  #248
                  I found the SSPACE basic 2.1 in GitHub, from one of the original devs, so no need to bother with Baseclear to use the -x=1

                  Comment

                  • milo0615
                    Member
                    • Dec 2012
                    • 39

                    #249
                    Originally posted by sunnycqcn View Post
                    I am sure the 3.0 version work well with the big genome. I assembled one genome last month, it worked well. Meanwhile, I met the same problem as same with you. So if your library file include a lot of libraries, the error file should be like as your error file. So if you can present your library file, I can know what it happen.
                    Hi sunnycqcn,

                    My libraries.txt file looks like the following:

                    gjHS bowtie GerJamesonii_HS_1_P.fastq GerJamesonii_HS_2_P.fastq 100 0.25 FR
                    gjGA bowtie GerJamesonii_1_P.fastq GerJamesonii_2_P.fastq 125 0.25 FR


                    Thank you,

                    -Milo

                    Comment

                    • sunnycqcn
                      Member
                      • Apr 2013
                      • 17

                      #250
                      How many libraries is in your libraries files.


                      Originally posted by milo0615 View Post
                      Hi sunnycqcn,

                      My libraries.txt file looks like the following:

                      gjHS bowtie GerJamesonii_HS_1_P.fastq GerJamesonii_HS_2_P.fastq 100 0.25 FR
                      gjGA bowtie GerJamesonii_1_P.fastq GerJamesonii_2_P.fastq 125 0.25 FR


                      Thank you,

                      -Milo

                      Comment

                      • sunnycqcn
                        Member
                        • Apr 2013
                        • 17

                        #251
                        Usually, you can try a small dataset firstly.
                        Then software work well, you can run lots of data.
                        I am sure that my data run well now.




                        Originally posted by milo0615 View Post
                        Hi sunnycqcn,

                        My libraries.txt file looks like the following:

                        gjHS bowtie GerJamesonii_HS_1_P.fastq GerJamesonii_HS_2_P.fastq 100 0.25 FR
                        gjGA bowtie GerJamesonii_1_P.fastq GerJamesonii_2_P.fastq 125 0.25 FR


                        Thank you,

                        -Milo

                        Comment

                        • darthsequencer
                          Member
                          • Feb 2012
                          • 35

                          #252
                          Hi - I have a question about the "-n" option.

                          Here's what the option does: "minimum overlap required between contigs to merge adjacent contigs"

                          Does this mean that the SSPACE will assemble to contigs together that have terminal overlaps - like minimus2 would do?

                          Comment

                          • uloeber
                            Member
                            • Mar 2013
                            • 44

                            #253
                            Hi all,
                            What am I doing wrong if I get:

                            READING READS lib1:
                            ------------------------------------------------------------
                            Total inserted pairs = 3413702
                            Number of pairs containing N's = 17688
                            Remaining pairs = 3396014
                            ------------------------------------------------------------



                            LIBRARY lib1 STATS:
                            ################################################################################

                            MAPPING READS TO CONTIGS:
                            ------------------------------------------------------------
                            Number of single reads found on contigs = 0
                            Number of pairs used for pairing contigs / total pairs = 0 / 0
                            ------------------------------------------------------------

                            READ PAIRS STATS:
                            Assembled pairs: 0 (0 sequences)
                            Satisfied in distance/logic within contigs (i.e. -> <-, distance on target: 600 +/-60): 0
                            Unsatisfied in distance within contigs (i.e. distance out-of-bounds): 0
                            Unsatisfied pairing logic within contigs (i.e. illogical pairing ->->, <-<- or <-->): 0
                            ---
                            Satisfied in distance/logic within a given contig pair (pre-scaffold): 0
                            Unsatisfied in distance within a given contig pair (i.e. calculated distances out-of-bounds): 0
                            ---
                            Total satisfied: 0 unsatisfied: 0


                            Estimated insert size statistics (based on 0 pairs):
                            Mean insert size = 0
                            Median insert size = 0
                            REPEATS:
                            Number of repeated edges = 0
                            ------------------------------------------------------------
                            ?
                            Thanks in advance!
                            Ulrike

                            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
                              ...
                              Yesterday, 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, Today, 10:52 AM
                            0 responses
                            8 views
                            0 reactions
                            Last Post SEQadmin2  
                            Started by SEQadmin2, Yesterday, 05:39 AM
                            0 responses
                            17 views
                            0 reactions
                            Last Post SEQadmin2  
                            Started by SEQadmin2, 10-13-2026, 09:56 AM
                            0 responses
                            15 views
                            0 reactions
                            Last Post SEQadmin2  
                            Started by SEQadmin2, 10-09-2026, 11:14 AM
                            0 responses
                            27 views
                            0 reactions
                            Last Post SEQadmin2  
                            Working...