Header Leaderboard Ad

Collapse

Rfam/infernal help running

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • Rfam/infernal help running

    Hi all,

    I am trying to use rfam to search for sequence homologs to many small RNAs (read lists of about 50,000 sequences).

    I have successfully installed infernal and downloaded the rfam database. I am unclear on if/how I need to prepare the rfam database using cmbuild, cmcalibrate, and cmsearch. (I saw this in a tutorial for searching a sequence database with a single covariance model). When I tried this, cmbuild worked but cmcalibrate gave an error. Or, is rfam already in the correct format? If so, what are the steps to run a search? Or can you point me to the appropriate tutorial?

    Any help on how to run rfam using infernal would be greatly appreciated!

    Thanks very much,
    Claire

  • #2
    What exactly is the error?

    Running it is easy, if you use the perl script provided at the website (rfam_scan.pl).

    Command:
    perl rfam_scan.pl -blastdb /home/Data/RFAM/Rfam.fasta -o /home/Data/RFAM_output.txt --bt 0.0001 --nobig /home/Data/RFAM/Rfam.cm /home/Data/input.fasta

    (evalue: empirical from my site; --nobig: Doesn't scan for the big rRNA subunits; rnammer is way faster for that)

    Comment


    • #3
      Hi Claire,

      if you have downloaded the Rfam.cm from the Rfam website (ftp://ftp.ebi.ac.uk/pub/databases/Rfam/12.0/), then you only have to run cmpress on the Rfam.cm file to prepare it for cmscan (infernal v1.1).

      Comment

      Latest Articles

      Collapse

      • seqadmin
        Targeted Sequencing: Choosing Between Hybridization Capture and Amplicon Sequencing
        by seqadmin




        Targeted sequencing is an effective way to sequence and analyze specific genomic regions of interest. This method enables researchers to focus their efforts on their desired targets, as opposed to other methods like whole genome sequencing that involve the sequencing of total DNA. Utilizing targeted sequencing is an attractive option for many researchers because it is often faster, more cost-effective, and only generates applicable data. While there are many approaches...
        03-10-2023, 05:31 AM
      • seqadmin
        Expert Advice on Automating Your Library Preparations
        by seqadmin



        Using automation to prepare sequencing libraries isn’t a new concept, and most researchers are aware that there are numerous benefits to automating this process. However, many labs are still hesitant to switch to automation and often believe that it’s not suitable for their lab. To combat these concerns, we’ll cover some of the key advantages, review the most important considerations, and get real-world advice from automation experts to remove any lingering anxieties....
        02-21-2023, 02:14 PM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by seqadmin, 03-17-2023, 12:32 PM
      0 responses
      8 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 03-15-2023, 12:42 PM
      0 responses
      17 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 03-09-2023, 10:17 AM
      0 responses
      66 views
      1 like
      Last Post seqadmin  
      Started by seqadmin, 03-03-2023, 12:03 PM
      0 responses
      64 views
      0 likes
      Last Post seqadmin  
      Working...
      X