Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • SWP
    Member
    • Nov 2010
    • 20

    #1

    Dnaa

    Hello-

    Trying to install DNAA here. Following instructions in install I get the following error below. It appears that it's not finding BError.c, however, BError.c is found at the exact path it where it says it can't be found. I'm installing as root, so shouldn't be a permissions problem. Any advice would be awesome, thanks!

    make all-recursive
    make[1]: Entering directory `/home/user/software/dnaa-0.1.2'
    Making all in dkbaseencoding
    make[2]: Entering directory `/home/user/software/dnaa-0.1.2/dkbaseencoding'
    gcc -DHAVE_CONFIG_H -I. -I.. -Wall -g -O2 -pthread -D_IOLIB=2 -D_FILE_OFFSET_BITS=64 -m64 -MT dkbaseencoding.o -MD -MP -MF .deps/dkbaseencoding.Tpo -c -o dkbaseencoding.o dkbaseencoding.c
    mv -f .deps/dkbaseencoding.Tpo .deps/dkbaseencoding.Po
    make[2]: *** No rule to make target `../bfast/bfast/BError.c', needed by `BError.o'. Stop.
    make[2]: Leaving directory `/home/user/software/dnaa-0.1.2/dkbaseencoding'
    make[1]: *** [all-recursive] Error 1
    make[1]: Leaving directory `/home/user/software/dnaa-0.1.2'
    make: *** [all] Error 2
  • nilshomer
    Nils Homer
    • Nov 2008
    • 1283

    #2
    Originally posted by SWP View Post
    Hello-

    Trying to install DNAA here. Following instructions in install I get the following error below. It appears that it's not finding BError.c, however, BError.c is found at the exact path it where it says it can't be found. I'm installing as root, so shouldn't be a permissions problem. Any advice would be awesome, thanks!

    make all-recursive
    make[1]: Entering directory `/home/user/software/dnaa-0.1.2'
    Making all in dkbaseencoding
    make[2]: Entering directory `/home/user/software/dnaa-0.1.2/dkbaseencoding'
    gcc -DHAVE_CONFIG_H -I. -I.. -Wall -g -O2 -pthread -D_IOLIB=2 -D_FILE_OFFSET_BITS=64 -m64 -MT dkbaseencoding.o -MD -MP -MF .deps/dkbaseencoding.Tpo -c -o dkbaseencoding.o dkbaseencoding.c
    mv -f .deps/dkbaseencoding.Tpo .deps/dkbaseencoding.Po
    make[2]: *** No rule to make target `../bfast/bfast/BError.c', needed by `BError.o'. Stop.
    make[2]: Leaving directory `/home/user/software/dnaa-0.1.2/dkbaseencoding'
    make[1]: *** [all-recursive] Error 1
    make[1]: Leaving directory `/home/user/software/dnaa-0.1.2'
    make: *** [all] Error 2
    Show an "ls -alh" of your root DNAA directory. Did you make sure to follow the install instructions in INSTALL exactly?

    Comment

    • SWP
      Member
      • Nov 2010
      • 20

      #3
      Originally posted by nilshomer View Post
      Show an "ls -alh" of your root DNAA directory. Did you make sure to follow the install instructions in INSTALL exactly?
      Almost exactly, I already had samtools and bfast installed and in my path, and I added the sym link for bfast.

      Here's the ls...

      drwxr-xr-x 10 501 cdrom 4.0K 2011-04-05 09:09 .
      drwxr-xr-x 15 user users 4.0K 2011-04-05 09:08 ..
      -rw-r--r-- 1 root root 34K 2011-04-05 09:08 aclocal.m4
      -rw-r--r-- 1 501 cdrom 102 2009-09-30 00:04 AUTHORS
      -rw-r--r-- 1 501 cdrom 45K 2009-09-30 00:04 autogen.sh
      drwxr-xr-x 2 root root 4.0K 2011-04-05 09:08 autom4te.cache
      -rw-r--r-- 1 501 cdrom 244 2010-04-28 22:30 ChangeLog
      drwxr-xr-x 2 501 cdrom 4.0K 2011-04-05 09:08 config
      -rw-r--r-- 1 root root 4.2K 2011-04-05 09:09 config.h
      -rw-r--r-- 1 root root 3.9K 2011-04-05 09:08 config.h.in
      -rw-r--r-- 1 501 cdrom 3.8K 2010-08-28 17:42 config.h.in~
      -rw-r--r-- 1 root root 28K 2011-04-05 09:09 config.log
      -rwxr-xr-x 1 root root 34K 2011-04-05 09:09 config.status
      -rwxr-xr-x 1 501 cdrom 198K 2011-04-05 09:08 configure
      -rw-r--r-- 1 501 cdrom 4.0K 2010-08-28 17:42 configure.ac
      -rw-r--r-- 1 501 cdrom 83 2009-09-30 00:04 COPYING
      drwxr-xr-x 3 501 cdrom 4.0K 2011-04-05 09:09 dkbaseencoding
      drwxr-xr-x 2 501 cdrom 4.0K 2011-04-05 09:08 dlib
      drwxr-xr-x 3 501 cdrom 4.0K 2011-04-05 09:09 dqc
      drwxr-xr-x 3 501 cdrom 4.0K 2011-04-05 09:09 dtranslocations
      drwxr-xr-x 3 501 cdrom 4.0K 2011-04-05 09:09 dutil
      drwxr-xr-x 3 501 cdrom 4.0K 2011-04-05 09:09 dwgsim
      -rw-r--r-- 1 501 cdrom 768 2010-04-07 09:21 INSTALL
      -rw-r--r-- 1 501 cdrom 18K 2009-09-30 00:04 LICENSE
      -rw-r--r-- 1 root root 24K 2011-04-05 09:09 Makefile
      -rw-r--r-- 1 501 cdrom 220 2010-04-28 17:03 Makefile.am
      -rw-r--r-- 1 root root 24K 2011-04-05 09:08 Makefile.in
      -rw-r--r-- 1 501 cdrom 28 2009-09-30 00:04 NEWS
      -rw-r--r-- 1 501 cdrom 2.4K 2010-04-07 09:21 README
      -rw-r--r-- 1 root root 23 2011-04-05 09:09 stamp-h1

      Comment

      • nilshomer
        Nils Homer
        • Nov 2008
        • 1283

        #4
        Where are the samtools and bfast symbolic links here? They should be in this directory.

        Comment

        • SWP
          Member
          • Nov 2010
          • 20

          #5
          thanks for your help <fixed>

          Got the sym links in the right place

          Comment

          • masterpiece
            Member
            • Mar 2009
            • 40

            #6
            Hi all,

            I found a blog showing how to set up the dnaa step by step. Hope this can solve the dnaa installation prob. BTW i've install under Fedora13 and its works

            Update finally got it to work. #prereqs GNU Autoconf version 2.59 GNU Automake version 1.9.6 GNU Libtool version 1.5.22 also requires...


            kamal

            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

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by SEQadmin2, 08-06-2026, 07:41 AM
            0 responses
            16 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 08-03-2026, 10:13 AM
            0 responses
            33 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-31-2026, 02:55 AM
            0 responses
            42 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...