Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • ffinkernagel
    Senior Member
    • Oct 2009
    • 110

    #16
    yeah, that's what the line with grep is supposed to check-whether that string abyss complains about is in there.

    Comment

    • Seta
      Member
      • Mar 2011
      • 14

      #17
      how long should that take..hours or just minutes...mine is already bussy for an hour...

      Comment

      • ffinkernagel
        Senior Member
        • Oct 2009
        • 110

        #18
        Well, for a 1.2 gig file (compressed), my machine needed about 3 minutes (transfering it on a gigabit network) for doing the 'gzip -cd | grep' stanca.

        Comment

        • Seta
          Member
          • Mar 2011
          • 14

          #19
          I don't get any output at all, if I use the line:
          gzip -cd s_7_sequence.fastq.gz | grep "Ms_7_sequence.txt"
          But I also already thought that there wouldn't be a line with "Ms_7_sequence.txt"....

          Comment

          • ffinkernagel
            Senior Member
            • Oct 2009
            • 110

            #20
            Yes, no output is what you would get if there was no 'Ms_7_sequence.txt' in there.

            Curiouser and curiouser - have you tried passing the un-gziped file (gzip -d name.fastq.gz) to AbySS?

            Comment

            • Seta
              Member
              • Mar 2011
              • 14

              #21
              That is weird!!! the last time I tried it din't work and now it is reading the file! I'll cross my fingers and hope for the best. Do you have any idea how long it could take? I read somewhere that it can take between 3 and 10 hours...

              Comment

              • ffinkernagel
                Senior Member
                • Oct 2009
                • 110

                #22
                that depends.
                What exactly are you trying to assemble, how many reads do you have, etc?.

                Generally, assembly can take a long (long) time.

                Comment

                • Dorisday81
                  Junior Member
                  • Jun 2011
                  • 1

                  #23
                  Hi all, I'm new here and have a problem.
                  Maybe its not right place to write but I can not write new post.

                  I'm using the ABySS for 36bp sequences and now will use the trans-ABySS.

                  I used command: for k in {18..35}; do ABYSS <file to analyze> -o <where save the file>-k@$k.fa;

                  My input was file with contigs (after format: fastanrdb) with FASTA extenstion.

                  I got from ABYSS analysis files. They looks like (examples):

                  >0 31 117
                  AGACTTCCCAACATTTATTGCTCTTTCTCTT
                  >1 35 79
                  ATGAATTCTATTGGAGATTGTACATTAGTTATGTA
                  >2 27 60
                  ATGAATTCTATTGGAGAATGTACATTA
                  >3 44 666
                  TTTTTATTTTTGTTCAGAAGGAGTCGTTGGTTGTTCTTCATTTT
                  >4 111 1332
                  GATGGTGTAATGAACTCAACAATATCATCTCTTATTACTATATCTGACCGTGCTTATGTAACATTAACTAATTACCAAGGATTGTATAGATTAAATTGTGACCAGAAAACT
                  >5 18 31
                  GGAGTGTCGATGCTTGAA
                  >6 38 213
                  GCAAATTCTGTTACAATTGATATTTCTCCTTCTGTATA


                  I have problem with next step of analysis-the trans-Abyss

                  In manual guide I read that the trans abyss needs specific folder structure.

                  I dont know what does it means, because I put my results from abyss (in fasta) in folders: LIB0001/kn(15-35)/...fasta (from abyss)

                  I dont know what is next?

                  sorry for so complicates question but I am so sad sitting, reading and nothing.....

                  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...