Details

    • Type: Task
    • Status: Closed (View Workflow)
    • Priority: Major
    • Resolution: Done
    • Affects Version/s: None
    • Fix Version/s: None
    • Labels:
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      Description

      GOAL:

      To use the newly annotated Trinity files as a REFERENCE to align reads to and determine gene expression for Kelsey's dataset.

      There are 4 newly generated Trinity sets of contigs (TMNH). See IGBF-3741.

      Want to run NEXTFLOW. One for each variety.

      Location of Trinity COntigs:
      /projects/tomato_genome/fnb/dataprocessing/trinity/NEXTFLOW/postblat
      (there should be 4 fasta files here, if not yet, soon.....)

      The reads that will be used are here:
      /projects/tomato_genome/rnaseq/renamed_Ravi_Combined

      Instead of running ALL reads, we be separating by variety.
      So only using the reads fr heinz with the Heinz trinity contig file......

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          Activity

          robofjoy Robert Reid created issue -
          robofjoy Robert Reid made changes -
          Field Original Value New Value
          Epic Link IGBF-2993 [ 21429 ]
          robofjoy Robert Reid made changes -
          Assignee Ann Loraine [ aloraine ] Robert Reid [ robertreid ]
          Hide
          robofjoy Robert Reid added a comment -

          This is a golden opportunity to test out Molly's pipeline document!

          Used this document to run the pipeline: https://docs.google.com/document/d/1ig9ET-ykXF5nAX3P487cXWmZDGUlQpcwrvFXpbyP5vw/edit

          And I will have Brandon try this out also and get familiar with the nextflow process.

          This time however we will not be aligning to SL4 or SL5 but to the Trinity contigs.

          Show
          robofjoy Robert Reid added a comment - This is a golden opportunity to test out Molly's pipeline document! Used this document to run the pipeline: https://docs.google.com/document/d/1ig9ET-ykXF5nAX3P487cXWmZDGUlQpcwrvFXpbyP5vw/edit And I will have Brandon try this out also and get familiar with the nextflow process. This time however we will not be aligning to SL4 or SL5 but to the Trinity contigs.
          robofjoy Robert Reid made changes -
          Status To-Do [ 10305 ] In Progress [ 3 ]
          Hide
          robofjoy Robert Reid added a comment -

          Need all the pieces for next flow:

          • A csv file for the files (Using data from (SRP499796) sample,fastq_1,fastq_2,strandedness
          • Fasta file of the trinity Contigs
          • A GTF file
          • A genebed file
          • The tomato config file

          Running this here: /projects/tomato_genome/fnb/dataprocessing/trinity/NEXTFLOW/hei-run1

          Copied tomato config file from Molly's runs.

          Got Fasts? Want GTF ? A perl script is hidden in the Trinity utils folder!! Works great.
          perl /apps/pkg/trinity/2.14.0/util/misc/cdna_fasta_file_to_transcript_gtf.pl tamaulipas-trinity.Trinity.fasta | grep -w "exon" - > Trinity.gtf

          Show
          robofjoy Robert Reid added a comment - Need all the pieces for next flow: A csv file for the files (Using data from (SRP499796) sample,fastq_1,fastq_2,strandedness Fasta file of the trinity Contigs A GTF file A genebed file The tomato config file Running this here: /projects/tomato_genome/fnb/dataprocessing/trinity/NEXTFLOW/hei-run1 Copied tomato config file from Molly's runs. Got Fasts? Want GTF ? A perl script is hidden in the Trinity utils folder!! Works great. perl /apps/pkg/trinity/2.14.0/util/misc/cdna_fasta_file_to_transcript_gtf.pl tamaulipas-trinity.Trinity.fasta | grep -w "exon" - > Trinity.gtf
          Hide
          robofjoy Robert Reid added a comment -

          After presenting a few of these results to Kevin, he suggested that we use tools other than Trinity for this process.

          Specifically, the tools RNA-Spades and RNA BLOOM 2.

          Going to end this task in favor of exploring these potentially better options.
          New tasks will be made for them.

          Show
          robofjoy Robert Reid added a comment - After presenting a few of these results to Kevin, he suggested that we use tools other than Trinity for this process. Specifically, the tools RNA-Spades and RNA BLOOM 2. Going to end this task in favor of exploring these potentially better options. New tasks will be made for them.
          robofjoy Robert Reid made changes -
          Status In Progress [ 3 ] Needs 1st Level Review [ 10005 ]
          robofjoy Robert Reid made changes -
          Status Needs 1st Level Review [ 10005 ] First Level Review in Progress [ 10301 ]
          robofjoy Robert Reid made changes -
          Status First Level Review in Progress [ 10301 ] Ready for Pull Request [ 10304 ]
          robofjoy Robert Reid made changes -
          Status Ready for Pull Request [ 10304 ] Pull Request Submitted [ 10101 ]
          robofjoy Robert Reid made changes -
          Status Pull Request Submitted [ 10101 ] Reviewing Pull Request [ 10303 ]
          robofjoy Robert Reid made changes -
          Status Reviewing Pull Request [ 10303 ] Merged Needs Testing [ 10002 ]
          robofjoy Robert Reid made changes -
          Status Merged Needs Testing [ 10002 ] Post-merge Testing In Progress [ 10003 ]
          robofjoy Robert Reid made changes -
          Resolution Done [ 10000 ]
          Status Post-merge Testing In Progress [ 10003 ] Closed [ 6 ]

            People

            • Assignee:
              robofjoy Robert Reid
              Reporter:
              robofjoy Robert Reid
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              • Created:
                Updated:
                Resolved: