Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • yu_chem
    Member
    • Mar 2015
    • 23

    #1

    How to install local blast on linux

    Hi everybody

    Now I’m bothered with setting of local blast-2.2.26 on linux
    Please help me. I'm beginner as bioinfomatician.

    I have downloaded local blast-2.2.26, homo_sapiens genome and Refseq from below sites.
    and use CentOS linux 7

    genome data from ensembl ftp://ftp.ensembl.org/pub/release-75...o_sapiens/dna/
    Refseq data from NCBI ftp://ftp.ncbi.nlm.nih.gov/genomes/H..._level.gff3.gz

    Now I have two problems.
    1.I don't know how to check proper combination of data between genome data and Refseq.
    2.I don't know how to make database for blast using above two data

    I think that actually user first combine two data into one file using 'cat' command and next use 'formatdb' command
    >formatdb -i input-file-name -n database-name -p F

    but I got following error
    [formatdb] WARNING: Sequence number 1 (lcl|1_input-file-name), 8139970 illegal characters were removed:
    54 Es, 114 Fs, 42 Is, 117 Js, 2 Ls, 114 Qs

    Please reply to above question.
    best regards
  • Richard Finney
    Senior Member
    • Feb 2009
    • 701

    #2
    That's a WARNING, not an ERROR.
    Did it create an output file?

    Comment

    • GenoMax
      Senior Member
      • Feb 2008
      • 7142

      #3
      Why bother creating your own when NCBI makes pre-formatted indexes available here: ftp://ftp.ncbi.nlm.nih.gov/blast/db/ Both human genomic and refseq db are available.

      Download the relevant files (there are multiple) for each set e.g. refseq_genomic.xx.tar.gz. Unzip/untar them and leave them all in a single folder. When doing the blast search use the "base name" as db name (e.g. refseq_genomic).

      Comment

      • yu_chem
        Member
        • Mar 2015
        • 23

        #4
        Dear Richard Finney.

        Thank you for answer and I' sorry about delay of the reply
        After I commanded formatdb, blast creates files: database-name.nsq, database-name.nhr and database-name.nin and then in formatdb.log, the below message was written.

        Version 2.2.26 [Sep-21-2011]
        Started database file "./data/Hchr-d.fa"
        WARNING: [000.000] Sequence number 24 (lcl|24_Hdata), 8139970 illegal characters were removed:
        54 Es, 114 Fs, 42 Is, 117 Js, 2 Ls, 114 Qs

        Formatted 24 sequences in volume 0
        SUCCESS: formatted database database-name

        But e.g. when I commanded ./bin/fastacmd -d database-name -s NC_000001.10 -L 100,500, the blow message was displayed.

        [fastacmd] ERROR: Entry "nc_000001.10" not found

        If I succeed in formatdb, why cann't I succeed in fastacmd?
        Last edited by yu_chem; 03-06-2015, 02:50 AM.

        Comment

        • yu_chem
          Member
          • Mar 2015
          • 23

          #5
          Dear Genomax

          Thank you for answer and I'm sorry for delay of the reply.
          I also try using other database.
          It's reason for selecting these files of genome and genes that when I started to learn bioinformatics, other researcher recommended to use these files NCIB refseq and ensembl genome data, But I didn't know the reason. Actually I should ask him, But he is busy. So I try install of local blast on my own.

          Comment

          Latest Articles

          Collapse

          • kinpict.com
            Reply to 16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
            by kinpict.com
            The part about this topic feels surprisingly grounded, and the details on the page is the bit that made me slow down. I’d keep <a href="https://kinpict.com/">ai family photo generator</a> bookmarked for later.
            Today, 06:37 PM
          • SEQadmin2
            16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
            by SEQadmin2





            NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification,...
            10-30-2026, 06:46 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by SEQadmin2, 11-12-2026, 07:59 AM
          0 responses
          27 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 11-05-2026, 09:25 AM
          0 responses
          35 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 11-03-2026, 11:54 AM
          2 responses
          56 views
          0 reactions
          Last Post kinpict.com  
          Started by SEQadmin2, 10-28-2026, 09:57 AM
          0 responses
          175 views
          0 reactions
          Last Post SEQadmin2  
          Working...