Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #16
    Files referred to in the last post by @Sajna are once again available at the same link.

    Comment

    • Sajna
      Member
      • Oct 2015
      • 14

      #17
      As per the RNASeq version 2 pipeline in the link below, I have been able to obtain outputs till step 11, i.e the transcriptome_alignments_filtered.bam output. Next step is to run rsem.



      I ran RSEM using the following command : /opt/rsem-1.1.13/rsem-calculate-expression --paired-end --bam --estimate-rspd -p 8 transcriptome_alignments_filtered.bam /home/group_sh/TCGA+SRA_datamergerquantification_RNASeqV2/RSEM_ref_from_TCGA_webshare/hg19_M_rCRS_ref ERR519523.rsem > rsem.log_2 > rsem.log

      I get this error in the log file :

      rsem-parse-alignments failed! Please check if you provide correct parameters/options for the pipeline!

      What is wrong? I donot understand. I am running exactly the same command!!!

      Kindly help.

      Comment

      • GenoMax
        Senior Member
        • Feb 2008
        • 7142

        #18
        Are you using a different version of RSEM than the one in the PDF?

        Comment

        • Sajna
          Member
          • Oct 2015
          • 14

          #19
          No. I am using the same version mentioned in the UNC mRNASeq version2 document.

          Comment

          • GenoMax
            Senior Member
            • Feb 2008
            • 7142

            #20
            Have you done first part of step 4 in this document: https://tcga-data.nci.nih.gov/tcgafi...ESCRIPTION.txt

            Comment

            • Sajna
              Member
              • Oct 2015
              • 14

              #21
              Yes, I have done the first part of step 4 from that doc. I have the transcripts_aligned.bam, furthur filtering is also done. The only thing thats not working is RSEM...which we need!!!

              Comment

              • GenoMax
                Senior Member
                • Feb 2008
                • 7142

                #22
                Write directly to the contacts included in the TCGA doc with a request for help.

                Comment

                • Sajna
                  Member
                  • Oct 2015
                  • 14

                  #23
                  Ok. I will do that. Will update on the same once I receive the reply. Thanks.

                  Comment

                  Latest Articles

                  Collapse

                  • SEQadmin2
                    Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
                    by SEQadmin2






                    CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

                    Despite this, “CRISPR helped turn genome editing from a specialized
                    ...
                    07-31-2026, 11:01 AM
                  • SEQadmin2
                    Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
                    by SEQadmin2


                    Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

                    The systematic characterization of the human proteome has
                    ...
                    07-20-2026, 11:48 AM
                  • SEQadmin2
                    Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
                    by SEQadmin2



                    Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
                    ...
                    07-09-2026, 11:10 AM

                  ad_right_rmr

                  Collapse

                  News

                  Collapse

                  Topics Statistics Last Post
                  Started by SEQadmin2, 07-31-2026, 02:55 AM
                  0 responses
                  20 views
                  0 reactions
                  Last Post SEQadmin2  
                  Started by SEQadmin2, 07-24-2026, 12:17 PM
                  0 responses
                  16 views
                  0 reactions
                  Last Post SEQadmin2  
                  Started by SEQadmin2, 07-23-2026, 11:41 AM
                  0 responses
                  16 views
                  0 reactions
                  Last Post SEQadmin2  
                  Started by SEQadmin2, 07-20-2026, 11:10 AM
                  0 responses
                  26 views
                  0 reactions
                  Last Post SEQadmin2  
                  Working...