Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • illuminaGA
    Member
    • Dec 2012
    • 71

    #1

    How to save/export BSMAP run info?

    Dear All

    I am new for bioinfo and Linux system.

    When BSMAP finished. I usually got some running information form terminal like this.

    Load in 2739 db seqs, total size 2909698938 bp. 46 secs passed
    total_kmers: 43046721
    Create seed table. 193 secs passed
    max number of mismatches: read_length * 8% max gap size: 0
    kmer cut-off ratio: 5e-07
    max multi-hits: 2 max Ns: 5 seed size: 16 index interval: 4
    quality cutoff: 20 base quality char: '!'
    min fragment size:28 max fragemt size:500
    start from read #1 end at read #4294967295
    additional alignment: T in reads => C in reference
    mapping strand: ++,-+
    Single-end alignment(8 threads)
    Input read file: /run/media/qingsong/MyBook/Jendai/Brain_GSE50077_MBD_Seq/PILO_and_KD/2_SRR955124_207.fastq (format: FASTQ)
    Output file: /home/qingsong/Documents/wli/bsmap_Jendai_project/Brain_GSE50077_MBD_Seq/PILO_and_KD/2_q20_r0_w2.sam (format: SAM)
    Thread #4: 300000 reads finished. 206 secs passed
    Thread #5: 100000 reads finished. 206 secs passed
    Thread #2: 350000 reads finished. 207 secs passed
    Thread #7: 200000 reads finished. 207 secs passed
    .........
    .........
    Thread #2: 22459469 reads finished. 963 secs passed
    Thread #6: 22350000 reads finished. 964 secs passed
    Thread #4: 22300000 reads finished. 964 secs passed
    Thread #3: 22400000 reads finished. 966 secs passed
    Thread #1: 22450000 reads finished. 966 secs passed
    Total number of aligned reads: 12036799 (54%)
    Done.
    Finished at Thu Jul 3 16:21:22 2014
    Total time consumed: 966 secs


    Actually I want to save/export the red highlight information to a file. I tried ">" in the end of command line in Terminal but the exported file was blank. Any one have idea about this? Thank you in advance!!
    Last edited by illuminaGA; 07-03-2014, 12:39 PM.
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    That's written to stderr, so do "2>" rather than ">".

    Comment

    • illuminaGA
      Member
      • Dec 2012
      • 71

      #3
      Originally posted by dpryan View Post
      That's written to stderr, so do "2>" rather than ">".
      Thank you so much! It works

      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, Yesterday, 07:41 AM
      0 responses
      11 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-03-2026, 10:13 AM
      0 responses
      25 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-31-2026, 02:55 AM
      0 responses
      38 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-24-2026, 12:17 PM
      0 responses
      25 views
      0 reactions
      Last Post SEQadmin2  
      Working...