Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • PhiX removal

    Hi all,
    I am trying to removed Phix reads from my miseq data but I keep on getting
    # reads processed: 839305
    # reads with at least one reported alignment: 0 (0.00%)
    # reads that failed to align: 839305 (100.00%)
    No alignments
    The bowtie command used is - bowtie PhiX_index --sam --al aligned.fq --un unaligned.fq -1 ~/misedata/phixinput/13_S13_L001_R1_001.fastq.out -2 ~/misedata/phixinput/13_S13_L001_R2_001.fastq.out S13.sam

    could someone tell me where the problem is?
    Thanks,
    Joshua

  • #2
    Your sequencing facility may have already removed the phiX sequences when they processed your data. The result you are looking at may be real i.e. there is no phiX sequence in your sample file. You should ask the facility if they have removed phiX sequences.
    Last edited by GenoMax; 07-30-2014, 04:41 AM.

    Comment


    • #3
      I agree with GenoMax - you probably do not have any phiX reads. If you want to test this out you could put part of phiX at the end of your read files (making copies of them first!) and see if you get one hit. In other words deliberately contaminate your reads.

      Comment


      • #4
        Can anyone please help me which web i can downloan PhiX genome fastq file?
        Thank you very much.

        Comment


        • #5
          From iGenomes (if you want Illumina's version, it is there): http://support.illumina.com/sequenci...e/igenome.html This is a package download with indexes etc but you will find the genome fasta file there. If you need it in fastq format then you could made a fake set of Q-scores.

          Comment


          • #6
            Thank you very much GenoMax

            Comment

            Latest Articles

            Collapse

            • seqadmin
              Recent Advances in Sequencing Analysis Tools
              by seqadmin


              The sequencing world is rapidly changing due to declining costs, enhanced accuracies, and the advent of newer, cutting-edge instruments. Equally important to these developments are improvements in sequencing analysis, a process that converts vast amounts of raw data into a comprehensible and meaningful form. This complex task requires expertise and the right analysis tools. In this article, we highlight the progress and innovation in sequencing analysis by reviewing several of the...
              Yesterday, 07:48 AM
            • seqadmin
              Essential Discoveries and Tools in Epitranscriptomics
              by seqadmin




              The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...
              04-22-2024, 07:01 AM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by seqadmin, Yesterday, 07:17 AM
            0 responses
            11 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 05-02-2024, 08:06 AM
            0 responses
            19 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-30-2024, 12:17 PM
            0 responses
            20 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-29-2024, 10:49 AM
            0 responses
            28 views
            0 likes
            Last Post seqadmin  
            Working...
            X