Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • cefanter
    Junior Member
    • Mar 2015
    • 2

    #1

    Appropriate Adapter Sequence fora trimming? RNAseq Transcriptome

    For previous studies I have contracted out both Illumina sequencing and RNAseq analysis of transcriptomes. An updated reference genome was added to NCBI this past year, and I want to take previously sequenced fastq files and realign them to the new reference genome in galaxy using Tophat and Cufflinks. I contacted the sequencing facilities to understand their protocol to determine if adapter sequences had been removed. They were unclear whether or not the trimming had already been executed, and their response time to my questions is lagging. They have however sent me this email.

    "We performed a polyA selection with a kit from Ambion: MicroPoly(A) Purist Kit; required 1000ng as starting material

    We used a cDNA kit from NuGEN: Ovation RNA-Seq System V2; we added 1ng of mRNA into the reaction. There is a SPIA adaptor sequence you will most likely want to trim off the 5' ends.
    We used an in house cocktail for the Illumina libraries (combination of kits from Lucigen and NEB); we initiated the Illumina libraries with 500ng of cDNA. We used the indexed Illumina adaptors:

    Multiplexing Adapters
    5' P-GATCGGAAGAGCACACGTCT
    5' ACACTCTTTCCCTACACGACGCTCTTCCGATCT

    Multiplexing PCR Primer 1.0
    5' AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT

    Multiplexing PCR Primer 2.0
    5' GTGACTGGAGTTCAGACGTGTGCTCTTCCGATCT

    PCR Primer, Index 1
    5’ CAAGCAGAAGACGGCATACGAGATXXXXXXGTGACTGGAGTTC

    Let me know if you have more questions.

    Thanks!
    Catrina


    Index Sequence - XXXXXX
    Sample Library
    GCCGCG CPAM-RS15-RS15-V1 CPAM-RS15-RS15-V1-cDNA-1-lib1a
    GCTCCA CPAM-RS14-RS14-CS1 CPAM-RS14-RS14-CS1-cDNA-1-lib1a
    GGCACA CPAM-RS9-RS9-CS1 CPAM-RS9-RS9-CS1-cDNA-1-lib1a
    GGCCTG CPAM-RS12-RS12-V1 CPAM-RS12-RS12-V1-cDNA-1-lib1a
    GTCCGC CPAM-RS11-RS11-CS1 CPAM-RS11-RS11-CS1-cDNA-1-lib1a
    TAATCG CPAM-RS11-RS11-V1 CPAM-RS11-RS11-V1-cDNA-1-lib1a
    TACAGC CPAM-RS16-RS16-V1 CPAM-RS16-RS16-V1-cDNA-1-lib1a
    TATAAT CPAM-RS13-RS13-CS1 CPAM-RS13-RS13-CS1-cDNA-1-lib1a
    Index Sequence - XXXXXX Sample Library
    CACCGG CPAM-RS12-RS12-CS1 CPAM-RS12-RS12-CS1-cDNA-2-lib2a
    CCTTAG CPAM-RS9-RS9-V1 CPAM-RS9-RS9-V1-cDNA-2-lib2a
    CTCAGA CPAM-RS8-RS8-CS1 CPAM-RS8-RS8-CS1-cDNA-2-lib2a
    CTGCTG CPAM-RS8-RS8-V1 CPAM-RS8-RS8-V1-cDNA-2-lib2a
    GACGGA CPAM-RS13-RS13-V1 CPAM-RS13-RS13-V1-cDNA-2-lib1a
    GATATA CPAM-RS14-RS14-V1 CPAM-RS14-RS14-V1-cDNA-2-lib1a
    GATGCT CPAM-RS15-RS15-CS1 CPAM-RS15-RS15-CS1-cDNA-2-lib1a
    GTAGAG CPAM-RS16-RS16-CS1 CPAM-RS16-RS16-CS1-cDNA-2-lib1a "

    I want to make sure that there is no contamination of adapter sequences, even though the quality of my reads is high. I have tried creating a fasta file using the Multiplexing Adapters sequences listed above, and attempting trimming using Scythe, however the output file always is empty. Am I using the correct sequences? Do I need to trim individual fastq files using their appropriate indexes? I am still new to the process, so any advice would be appreciated.
  • Brian Bushnell
    Super Moderator
    • Jan 2014
    • 2709

    #2
    I recommend creating a fasta file with all the sequences, except for the one with XXXXXX, make a copy of that with each index - GCCGCG, GCTCCA, etc. Then trim all of your reads with the same fasta file. Sometimes there is confusion about which orientation the adapters will be read in, so it may also be useful to try the reverse-complements as well if scythe doesn't do that automatically.

    If the reads have never been trimmed in any way, they will all be the same length.

    Comment

    • cefanter
      Junior Member
      • Mar 2015
      • 2

      #3
      Brian,

      Thanks for the advice.

      I am still having problems with trimming using the tool scythe in a local host galaxy. I went ahead and created a fasta file containing all of the adapters and their reverse sequences. The resulting output has a description of "no peek" and is empty. The fasta file is in the proper format with each adapter identification line starting with a ">" and a following line of sequence containing only basepair letters (see attached).

      Is this an internal problem with scythe downloaded to galaxy? would another tool be more appropriate for my need of trimming out adapters? What causes this no peek result?
      Attached Files

      Comment

      • Brian Bushnell
        Super Moderator
        • Jan 2014
        • 2709

        #4
        Your adapter file appears to be valid. Unfortunately, I don't use Galaxy or Scythe, so I'm not sure what the problem might be, or what "no peek" is supposed to mean. If you are able to process your data on the command line, I suggest you try running BBDuk, like this:

        bbduk.sh in=reads.fastq out=trimmed.fastq ref=adapters.txt ktrim=r k=23 mink=11 hdist=1

        Comment

        • GenoMax
          Senior Member
          • Feb 2008
          • 7142

          #5
          I don't have access to a galaxy with scythe installed but I think this may be a problem with your local galaxy. Have you asked your local galaxy admins/support for help?

          There are many tools that can trim but you will need to work outside galaxy.

          Comment

          Latest Articles

          Collapse

          • SEQadmin2
            Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
            by SEQadmin2



            Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

            Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
            ...
            10-14-2026, 09:55 AM
          • SEQadmin2
            New Genomics Technologies Take Aim at Long-Standing Limits
            by SEQadmin2


            Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

            We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
            ...
            09-28-2026, 10:25 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by SEQadmin2, 10-22-2026, 11:13 AM
          0 responses
          26 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 10-22-2026, 10:48 AM
          0 responses
          20 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 10-15-2026, 10:52 AM
          0 responses
          36 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 10-14-2026, 05:39 AM
          0 responses
          43 views
          0 reactions
          Last Post SEQadmin2  
          Working...