Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • lgoff
    Member
    • Feb 2008
    • 82

    #31
    Originally posted by AddDNAse View Post
    Hi everyone,

    I hope someone is still checking this thread. I am having a very similar problem. I have tried all of the troubleshoots posted here. I keep getting the following:
    tracking_id gene_short_name
    1 XLOC_000010 <NA>
    2 XLOC_000011 <NA>
    3 XLOC_000013 <NA>
    4 XLOC_000014 <NA>
    5 XLOC_000018 <NA>
    6 XLOC_000022 <NA>
    Hi AddDNAse, Can you provide a bit more context here. How are you generating this list of tracking_id and gene_short_names. Can you find a gene by gene_short_name using findGene()? Can you post a bit more of the code to provide a better description of what's going on.

    Thanks,
    Loyal

    Comment

    • AddDNAse
      Junior Member
      • May 2014
      • 3

      #32
      Hi Loyal,

      First of all, I'm using the S. cerevisiae annotation and genome from Ensembl (found on the Cufflinks website). I have modified the annotation to include a few smallRNAs.

      This list I posted was done using the following code:
      Code:
      gene_diff_data<-diffData(genes(cuff_data))
      sig_gene_data<-subset(gene_diff_data, (significant == 'yes'))
      diffGenes<-getGenes(cuff_data, sig_gene_data$gene_id)
      head(featureNames(diffGenes),n=3)
      I also tried doing the following:
      Code:
      gene.features<-annotation(genes(cuff))
      head(gene.features)
      Where I get the same result (almost all are 'NA' for gene_short_name with a few exceptions).

      Originally posted by lgoff View Post
      Hi AddDNAse, Can you provide a bit more context here. How are you generating this list of tracking_id and gene_short_names. Can you find a gene by gene_short_name using findGene()? Can you post a bit more of the code to provide a better description of what's going on.

      Thanks,
      Loyal
      Hope this is enough info? Thanks!
      Last edited by AddDNAse; 05-14-2014, 02:02 PM.

      Comment

      • david.eby
        Junior Member
        • Sep 2012
        • 3

        #33
        Hi everyone,

        I'm just posting this for the benefit of anyone looking for help on the topic in the future. I worked out a variation of the code posted earlier by Thomas but modified to handle merging in the face of duplicate lines in the table. Here's a simplified version of what we're using in GenePattern for the CummeRbund.QcReport module (currently in Beta):
        Code:
              feature.level <- "genes"
                 # ... or "isoforms", "TSS", "CDS"
              idColumnName <- "gene_id"
                 # ... or "isoform_id", "TSS_group_id", "CDS_id" to match above
              report.name <- paste0('QC.sig_diffExp_', feature.level,'.txt')
                 # ... or whatever you want
              
              cuff <- readCufflinks()
              sigIDs <- getSig(cuff,level=feature.level,alpha=0.05)
              if (NROW(sigIDs) > 0) {
                 sigFeatures <- getFeatures(cuff,sigIDs,level=feature.level)
                 sigData <- diffData(sigFeatures)
                 sigData <- subset(sigData, (significant == 'yes'))
                 names <- featureNames(sigFeatures)
                 sigOutput <- merge(names, sigData, by.x="tracking_id", 
                                    by.y=idColumnName)
                 
                 # Patch the merged table to have the original name for the ID column.  
                 # This is always the first column for the examples we've seen.
                 colnames(sigOutput)[1] <- idColumnName
                 write.table(sigData, report.name, sep='\t', row.names = F, 
                             col.names = T, quote = F)
              }
        The point here is to write a report file containing the table, but one could obviously use the sigOutput object directly instead.

        Here is similar code to do likewise for the distValue reports:
        Code:
              dist.selector.function <- promoters
                 # ... or splicing or relCDS
                 # Note that this is a function name, not a String!
              feature.level <- "genes"
                 # use "isoforms" for splicing, "genes" for promoter and relCDS
              report.name <- "QC.sig_promoter_data.txt"
                 # ... or whatever you want
        
              distData <- distValues(dist.selector.function(cuff))
              sigData <- subset(distData, (significant == 'yes'))
              if (nrow(sigData) > 0) {
                 sigIDs <- sigData[[1]]
                 sigFeatures <- getFeatures(cuff,sigIDs,level=feature.level)
                 names <- featureNames(sigFeatures)
                 sigOutput <- merge(names, sigData, by.x="tracking_id", 
                                    by.y=idColumnName)
                 colnames(sigOutput)[1] <- idColumnName
                 write.table(sigData, report.name, sep='\t', row.names = F, 
                             col.names = T, quote = F)
              }
        Just for reference, the above is for R 2.15.3, Bioconductor 2.11 and cummeRbund 2.0.0. Hope it helps someone!

        Comment

        • NRB
          Junior Member
          • Mar 2020
          • 1

          #34
          Hi can someone help me. I am student still learning on R. Doing a DEG analysis. i want to visualize my DEG data got from cuffdiff 2.0... When want to create Gene Set Obeject, an error occurs


          enes<-getGenes(cuffCan,myGeneIds)
          Getting gene information:
          FPKM
          Error: near ")": syntax error
          In addition: Warning message:
          Closing open result set, pending rows



          Im not sure where is the syntax error. Could someone guide me through it

          Comment

          Latest Articles

          Collapse

          • mylaser
            Reply to Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
            by mylaser
            Kheloyaar: The Complete Guide to Kheloyaar Loginand Kheloyaar ID
            The online gaming industry has transformed the way people enjoy digital entertainment. As technology continues to improve, players are looking for platforms that offer convenience, security, and a seamless user experience. Kheloyaarhas gained attention among users who value an easy-to-use platform, quick account access, and a simple registration process.
            Whether you're exploring Kheloyaar for the first time or want to understand...
            Today, 09:27 PM
          • 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.
            ...
            Today, 11:10 AM
          • SEQadmin2
            Cancer Drug Resistance: The Lingering Barrier to Rising Survival
            by SEQadmin2



            Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.

            There is no single reason why many patients don’t respond to treatment as expected. Cancer is...
            Yesterday, 05:17 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by SEQadmin2, Today, 10:04 AM
          0 responses
          8 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, Yesterday, 10:08 AM
          0 responses
          7 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 07-07-2026, 11:05 AM
          0 responses
          10 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 07-02-2026, 11:08 AM
          0 responses
          31 views
          0 reactions
          Last Post SEQadmin2  
          Working...