Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Read length of different illumina machines

    Dear All,
    I was wondering about the read length of different illumina instruments like:

    Illumina GAIIx read length of 150+150
    Illumina HiSeq read length of 100+100

    But I also had paired/single end reads ( not mate pairs for sure) with a read length of 27-36, Does anyone knows which illumina machines produced those ?

    Cheers,
    seq_g

  • #2
    Originally posted by Seq_g View Post
    Dear All,
    I was wondering about the read length of different illumina instruments like:

    Illumina GAIIx read length of 150+150
    Illumina HiSeq read length of 100+100

    But I also had paired/single end reads ( not mate pairs for sure) with a read length of 27-36, Does anyone knows which illumina machines produced those ?

    Cheers,
    GAIIx maxed out at 76 bp reads in our hands. 36 bp runs were the norm early on. We also ran 50 bp.

    HiSeq runs can be of varying length. In general, SE/PE/Multiplex 50bp to 150bp (on the HiSeq 2500 variant) would be common lengths at this time.

    It would be difficult to know for sure but the reads you describe (27-36) could possibly have come from a GAII or GAIIx, specially if they are not of a recent vintage.

    Comment


    • #3
      The GA, HiSeq, and MiSeq can all give you those 27-36 bp reads, but most likely it's GA or early HiSeq data. You should be able to roughly tell what machine was used from the sequence ID in the fastq file. I can't say for sure that it was always like this, but all current fastq files from Illumina instruments incorporate the sequencer's serial number in the ID

      To give an example, for files coming off our MiSeq the sequence IDs all begin with @Mxxxxx. The M indicates the instrument is a MiSeq, and the serial # is the xxxxx. HiSeqs are HWI if I'm remembering this off the top of my head correctly.

      Comment


      • #4
        Originally posted by mcnelson.phd View Post
        The GA, HiSeq, and MiSeq can all give you those 27-36 bp reads, but most likely it's GA or early HiSeq data. You should be able to roughly tell what machine was used from the sequence ID in the fastq file. I can't say for sure that it was always like this, but all current fastq files from Illumina instruments incorporate the sequencer's serial number in the ID

        To give an example, for files coming off our MiSeq the sequence IDs all begin with @Mxxxxx. The M indicates the instrument is a MiSeq, and the serial # is the xxxxx. HiSeqs are HWI if I'm remembering this off the top of my head correctly.
        You're correct. HiSeq read headers start off with @HWI-ST, while GA reads start with @HWUSI-EAS. These names refer to the fact that the instrument was built in Hayward, CA as well as the codename used during development.

        Comment


        • #5
          Thank you every one. Your reply's helped me
          seq_g

          Comment

          Latest Articles

          Collapse

          • seqadmin
            Current Approaches to Protein Sequencing
            by seqadmin


            Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
            04-04-2024, 04:25 PM
          • seqadmin
            Strategies for Sequencing Challenging Samples
            by seqadmin


            Despite advancements in sequencing platforms and related sample preparation technologies, certain sample types continue to present significant challenges that can compromise sequencing results. Pedro Echave, Senior Manager of the Global Business Segment at Revvity, explained that the success of a sequencing experiment ultimately depends on the amount and integrity of the nucleic acid template (RNA or DNA) obtained from a sample. “The better the quality of the nucleic acid isolated...
            03-22-2024, 06:39 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by seqadmin, 04-11-2024, 12:08 PM
          0 responses
          24 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 10:19 PM
          0 responses
          25 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 09:21 AM
          0 responses
          21 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-04-2024, 09:00 AM
          0 responses
          52 views
          0 likes
          Last Post seqadmin  
          Working...
          X