Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • AndyOD
    Junior Member
    • Mar 2010
    • 3

    blast

    Hi,

    Probably a basic question.
    I have a file which contains 3 nucleotide sequences.These 3 sequences have been aligned using MUSCLE.

    I now want to blast this FILE, as opposed to each gene seperately, against a database of nucleotide sequences, is this possible?

    SO basically i want my query to be the file and db to be a massive database of various organisms?



    Thanks
    Andy
  • flxlex
    Moderator
    • Nov 2008
    • 412

    #2
    This is possible both for the web-based blast, as well as for the stand-alone blast. However, you will need to convert your sequences to fasta format.

    On the web, just paste the sequences into the query window. The stand-alone (blastall) will take your input file no matter how many sequences it contains.

    Happy blasting,

    flxlex

    Comment

    • AndyOD
      Junior Member
      • Mar 2010
      • 3

      #3
      the reply is very much appreciated.

      I think its posibly a little more tricky and involving some kind of profile building?

      So I have a file, it has three sequences.I don't want to compare each sequence in that file to a database, but rather I want to see how similar the 3 sequences combined are to a database.

      So to do that, I made an alignment of the three sequences.

      The next step would be to build a profile of the alignment and then blast the profile against the database, but I can't seem to find any program that builds profiles from nucleotides, prophecy etc. seem to be protein-based?

      Confused

      Comment

      • krobison
        Senior Member
        • Nov 2007
        • 734

        #4
        It does sound like you wish to build a profile.

        First, make sure you understand what you are really trying to do. Why do you believe combining the three sequences will improve sensitivity or specificity or both? What is the underlying pattern you are trying to detect?

        There are a host of nucleotide profile building & search tools (e.g. MEME, AlignACE), many of which are focused on looking for short motifs such as transcription factor binding sites. Is this what you expect to find?

        Alternatively, you can post-process the BLAST output to ask what sequences were matched by the aligned regions of you queries. If you don't believe there is a sensitivity gain from building a profile, this might give you the required specificity.

        AFAIK, there is no mode of BLAST to search nucleotide profiles, but I haven't tracked development of BLAST closely for a while & so could easily be wrong. There are programs to search profiles vs. DNA or can be used to build such profiles; I'm pretty sure HMMER is not strictly protein-based (but again, that hasn't tended to be its main use).

        You might also ask whether for what you are looking primary sequence is the most conserved feature. If secondary structure is important, there are other profile construction & search tools at the Eddy lab (HMMER builders) which are more appropriate in that circumstance.

        Comment

        Latest Articles

        Collapse

        • GATTACAT
          Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
          by GATTACAT
          Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
          07-01-2026, 11:43 AM
        • SEQadmin2
          Nine Things a Sample Prep Scientist Thinks About Before Sequencing
          by SEQadmin2


          I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

          Here are nine questions we think about, in roughly the order they matter, before...
          06-18-2026, 07:11 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, Yesterday, 11:08 AM
        0 responses
        6 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 06-30-2026, 05:37 AM
        0 responses
        11 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 06-26-2026, 11:10 AM
        0 responses
        19 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 06-17-2026, 06:09 AM
        0 responses
        53 views
        0 reactions
        Last Post SEQadmin2  
        Working...