Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • diegobonatto
    Junior Member
    • Mar 2014
    • 9

    Changing text in a GTF

    Hi,

    I have the following GTF file (from Gencode):
    HTML Code:
    chr10	Yale_UCSC	transcript	3117806	3119013	.	-	.	gene_id "PGOMOU00000268019"; transcript_id "PGOMOU00000268019"; gene_type "pseudogene"; gene_status "UNKNOWN"; gene_name "PGOMOU00000268019"; transcript_type "pseudogene"; transcript_status "UNKNOWN"; transcript_name "PGOMOU00000268019"; level 3; tag "2way_pseudo_cons"; yale_id "PGOMOU00000268019"; ucsc_id "NM_019986.3-3"; parent_id "ENSMUSG00000021476
    ";
    chr10	Yale_UCSC	transcript	3139466	3141067	.	-	.	gene_id "PGOMOU00000268020"; transcript_id "PGOMOU00000268020"; gene_type "pseudogene"; gene_status "UNKNOWN"; gene_name "PGOMOU00000268020"; transcript_type "pseudogene"; transcript_status "UNKNOWN"; transcript_name "PGOMOU00000268020"; level 3; tag "2way_pseudo_cons"; yale_id "PGOMOU00000268020"; ucsc_id "BC036983.1-1"; parent_id "ENSMUSG00000028228
    ";
    I would like to change all "PGOMOU*" names for "ENSMUSG*". How it can be done in R or awk in an easy way? Sorry for naive question, but I am struggling with awk to make the changes in GTF file. PGOMOU* nomenclature is not recognized by Bowtie/TopHat. So, any input is welcome!
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    Make a backup copy of the file before trying the following:

    Code:
    $ sed 's/PGOMOU/ENSMUSG/g' your_file > new_file
    Last edited by GenoMax; 08-22-2014, 10:38 AM.

    Comment

    • dpryan
      Devon Ryan
      • Jul 2011
      • 3478

      #3
      It's unlikely that changing this will solve whatever problem you're having. Post the actual problem and we'll try to solve it.

      Comment

      • diegobonatto
        Junior Member
        • Mar 2014
        • 9

        #4
        Thanks all!

        I'm trying to use the GTF file from Gencode that contain all pseudogenes predicted by the Yale & UCSC pipelines (but not by Havana on reference chromosomes) (ftp://ftp.sanger.ac.uk/pub/gencode/G...pseudos.gtf.gz) with the last GRCm38.p3 assembly, also from Gencode. The fastq files are OK. However, when I use Bowtie2, I'm always getting Bowtie error = 1, which could be related to PGOMOU gene nomenclature (my hypothesis). My first idea was to change all PGOMOU for ENSMUSG in order to allow Bowtie to recognize the same ID on genome...or I'm wrong?

        Comment

        • dpryan
          Devon Ryan
          • Jul 2011
          • 3478

          #5
          ENSMUSG* doesn't exist in the mouse genome (it's just used in the annotation). Please provide the exact command you used that produced the error and entire error message including the entire output that's printed to the screen.

          Comment

          • diegobonatto
            Junior Member
            • Mar 2014
            • 9

            #6
            Here it goes:

            HTML Code:
            tophat2 -p4 -G gencode.v20.2wayconspseudos.gtf -o MSCd0Adip-12 GRCh38 SRR490218_output2.fastq
            
            [2014-08-22 15:59:44] Beginning TopHat run (v2.0.9)
            -----------------------------------------------
            [2014-08-22 15:59:44] Checking for Bowtie
                              Bowtie version:        2.1.0.0
            [2014-08-22 15:59:44] Checking for Samtools
                            Samtools version:        0.1.19.0
            [2014-08-22 15:59:44] Checking for Bowtie index files (genome)..
            [2014-08-22 15:59:44] Checking for reference FASTA file
                    Warning: Could not find FASTA file GRCh38.fa
            [2014-08-22 15:59:44] Reconstituting reference FASTA file from Bowtie index
              Executing: /usr/bin/bowtie2-inspect GRCh38 > MSCd0Adip-12/tmp/GRCh38.fa
            [2014-08-22 16:02:05] Generating SAM header for GRCh38
                    format:          fastq
                    quality scale:   phred33 (default)
            [2014-08-22 16:03:07] Reading known junctions from GTF file
                    Warning: TopHat did not find any junctions in GTF file
            [2014-08-22 16:03:07] Preparing reads
                     left reads: min. length=60, max. length=66, 53983 kept reads (176 discarded)
            [2014-08-22 16:03:09] Building transcriptome data files..
            [2014-08-22 16:04:02] Building Bowtie index from gencode.v20.2wayconspseudos.fa
                    [FAILED]
            Error: Couldn't build bowtie index with err = 1
            The information is from the human GTF file and, of course, the last human genome assembly from Gencode, which generate an identical error for mouse. I'm running Bowtie together with TopHat (I known that is not necessary. Just only Bowtie is sufficient for alignment).

            thanks again!

            Comment

            • dpryan
              Devon Ryan
              • Jul 2011
              • 3478

              #7
              You can't expect an mouse annotation and a human reference sequence to be compatible (no amount of changing ID names will change that).

              Comment

              • diegobonatto
                Junior Member
                • Mar 2014
                • 9

                #8
                Yes, of course, but the example that I posted was for human (GTF AND genome) and the alignment was human Gencode pseudogene GTF with human genome assembly. When I tested the murine Gencode pseudogenes GTF AND murine genome (also from Gencode), I got the same Bowtie error.....If you look the example that I posted, the genome is from human and the GTF is from human. No murine genome OR murine GTF was used in that example.

                Comment

                • dpryan
                  Devon Ryan
                  • Jul 2011
                  • 3478

                  #9
                  Then look in the run log for the last command that tophat issued and run that yourself. You'll then get the actual underlying error message.

                  Comment

                  • diegobonatto
                    Junior Member
                    • Mar 2014
                    • 9

                    #10
                    And to reinforce that I'm not mixturing murine AND humans, each fastq is especific for each organism....

                    Again, any help is welcome!

                    Comment

                    • diegobonatto
                      Junior Member
                      • Mar 2014
                      • 9

                      #11
                      OK....TopHat indicated that "TopHat did not find any junctions in GTF file" and in run log the following command was used

                      PHP Code:
                      /usr/bin/tophat -p4 -G gencode.v20.2wayconspseudos.gtf -o MSCd0Adip-12 GRCh38 SRR490218_output2.fastq
                      /usr/bin/gtf_juncs gencode.v20.2wayconspseudos.gtf  MSCd0Adip-12/tmp/gencode.juncs
                      #>prep_reads:
                      /usr/bin/prep_reads --min-anchor 8 --splice-mismatches 0 --min-report-intron 50 --max-report-intron 500000 --min-isoform-fraction 0.15 --output-dir MSCd0Adip-12/ --max-multihits 20 --max-seg-multihits 40 --segment-length 25 --segment-mismatches 2 --min-closure-exon 100 --min-closure-intron 50 --max-closure-intron 5000 --min-coverage-intron 50 --max-coverage-intron 20000 --min-segment-intron 50 --max-segment-intron 500000 --read-mismatches 2 --read-gap-length 2 --read-edit-dist 2 --read-realign-edit-dist 3 --max-insertion-length 3 --max-deletion-length 3 -z gzip -p4 --gtf-annotations gencode.v20.2wayconspseudos.gtf --gtf-juncs MSCd0Adip-12/tmp/gencode.juncs --no-closure-search --no-coverage-search --no-microexon-search --fastq --aux-outfile=MSCd0Adip-12/prep_reads.info --index-outfile=MSCd0Adip-12/tmp/left_kept_reads.bam.index --sam-header=MSCd0Adip-12/tmp/GRCh38_genome.bwt.samheader.sam --outfile=MSCd0Adip-12/tmp/left_kept_reads.bam SRR490218_output2.fastq
                      #>map_start:
                      /usr/bin/gtf_to_fasta --min-anchor 8 --splice-mismatches 0 --min-report-intron 50 --max-report-intron 500000 --min-isoform-fraction 0.15 --output-dir MSCd0Adip-12/ --max-multihits 20 --max-seg-multihits 40 --segment-length 25 --segment-mismatches 2 --min-closure-exon 100 --min-closure-intron 50 --max-closure-intron 5000 --min-coverage-intron 50 --max-coverage-intron 20000 --min-segment-intron 50 --max-segment-intron 500000 --read-mismatches 2 --read-gap-length 2 --read-edit-dist 2 --read-realign-edit-dist 3 --max-insertion-length 3 --max-deletion-length 3 -z gzip -p4 --gtf-annotations gencode.v20.2wayconspseudos.gtf --gtf-juncs MSCd0Adip-12/tmp/gencode.juncs --no-closure-search --no-coverage-search --no-microexon-search gencode.v20.2wayconspseudos.gtf MSCd0Adip-12/tmp/GRCh38.fa MSCd0Adip-12/tmp/gencode.v20.2wayconspseudos.fa MSCd0Adip-12/logs/g2f.out
                      /usr/bin/bowtie2-build MSCd0Adip-12/tmp/gencode.v20.2wayconspseudos.fa MSCd0Adip-12/tmp/gencode.v20.2wayconspseudos 
                      Could it be possible that the search for junction by TopHat is inducing Bowtie error (again, my hypothesis. Excuse if it is to naive, but I'm struggling with this error at some days)?

                      Comment

                      • dpryan
                        Devon Ryan
                        • Jul 2011
                        • 3478

                        #12
                        Possible, is there anything in "MSCd0Adip-12/tmp/gencode.v20.2wayconspseudos.fa"?

                        Comment

                        • diegobonatto
                          Junior Member
                          • Mar 2014
                          • 9

                          #13
                          No, it empty....(0 bytes)

                          Comment

                          • dpryan
                            Devon Ryan
                            • Jul 2011
                            • 3478

                            #14
                            OK, now we're getting somewhere. That file is made by gtf_to_fasta, so something is going wrong with it. This could be the lack of junctions or it could be something else. Try running that command without the "--gtf-juncs MSCd0Adip-12/tmp/gencode.juncs" options and see what happens (I haven't a clue if it'll even run). If it runs, check to see if the resulting fasta files is empty or not.

                            Can you look through the GTF file and just see if you see any spliced transcripts? I wonder if tophat ignore pseudogenes.

                            Comment

                            • diegobonatto
                              Junior Member
                              • Mar 2014
                              • 9

                              #15
                              The comand did not work also...in fact, the GTF file just only contains spliced transcripts. Maybe running only with Bowtie alone should work. That's a weird problem...

                              Comment

                              Latest Articles

                              Collapse

                              • 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
                              • GATTACAT
                                Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
                                by GATTACAT
                                Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
                                07-01-2026, 11:43 AM
                              • SEQadmin2
                                Nine Things a Sample Prep Scientist Thinks About Before Sequencing
                                by SEQadmin2


                                I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

                                Here are nine questions we think about, in roughly the order they matter, before...
                                06-18-2026, 07:11 AM

                              ad_right_rmr

                              Collapse

                              News

                              Collapse

                              Topics Statistics Last Post
                              Started by SEQadmin2, Yesterday, 10:08 AM
                              0 responses
                              6 views
                              0 reactions
                              Last Post SEQadmin2  
                              Started by SEQadmin2, 07-07-2026, 11:05 AM
                              0 responses
                              8 views
                              0 reactions
                              Last Post SEQadmin2  
                              Started by SEQadmin2, 07-02-2026, 11:08 AM
                              0 responses
                              31 views
                              0 reactions
                              Last Post SEQadmin2  
                              Started by SEQadmin2, 06-30-2026, 05:37 AM
                              0 responses
                              29 views
                              0 reactions
                              Last Post SEQadmin2  
                              Working...