Header Leaderboard Ad

Collapse

How can I tell if 454 PE sequences in fasta file format have already been separated?

Collapse

Announcement

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

  • How can I tell if 454 PE sequences in fasta file format have already been separated?

    Hi

    I am new to bioinformatics and have never worked with 454 PE sequences before. I have 454 PE reads in fasta file format. The sequencing was done on the Roche 454 Titanium platform.

    My understanding is that 454 results are stored in .sff files, from which sequence and quality data must be extracted.

    Is it safe to assume, then, that if I have fasta files the forward and reverse ends have been separated already? I only have one file, not two.

    Is it possible for the ends to still be joined in the fasta file? If so, how can I tell if the PE sequences have been separated already?

    Can anyone suggest tools for doing the separation if I need to? I've found pyrocleaner and the NGS QC Toolkit, but I have no experience with either of them.

    thanks!

    E

  • #2
    You can tell if you either have multiple files for the reads, one with the left end and one with the right end, and perhaps a file with unsplittable (shotgun) reads. Or the names of the sequences can tell you, something like /1 and /2, or read1 and read2, or left and right, or whatever the splitting tool uses. You can splitt using sff_extract, or the newbler program from 454/Roche (perform and assembly and set the '-tr' option on).

    Comment


    • #3
      Why don't you just ask from whoever gave you the file?
      savetherhino.org

      Comment

      Latest Articles

      Collapse

      • seqadmin
        Improved Targeted Sequencing: A Comprehensive Guide to Amplicon Sequencing
        by seqadmin



        Amplicon sequencing is a targeted approach that allows researchers to investigate specific regions of the genome. This technique is routinely used in applications such as variant identification, clinical research, and infectious disease surveillance. The amplicon sequencing process begins by designing primers that flank the regions of interest. The DNA sequences are then amplified through PCR (typically multiplex PCR) to produce amplicons complementary to the targets. RNA targets...
        03-21-2023, 01:49 PM
      • 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

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by seqadmin, 03-24-2023, 02:45 PM
      0 responses
      16 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 03-22-2023, 12:26 PM
      0 responses
      17 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 03-17-2023, 12:32 PM
      0 responses
      17 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 03-15-2023, 12:42 PM
      0 responses
      24 views
      0 likes
      Last Post seqadmin  
      Working...
      X