tophat fusion error
0
0
Entering edit mode
5.1 years ago
dimitrischat ▴ 210

Hi all. Trying to run tophat fusion with 2 fastq files from rna-seq. I am using the example command from here: https://ccb.jhu.edu/software/tophat/fusion_tutorial.shtml .

tophat -o Output -p 10 --fusion-search --keep-fasta-order --bowtie1 --no-coverage-search -r 0 --mate-std-dev 80 --max-intron-length 100000 --fusion-min-dist 100000 --fusion-anchor-length 13 --fusion-ignore-chromosomes chrM '/home/app/..hg19bt1' S17_R1_001.fastq.gz S17_R2_001.fastq.gz

ERROR [2019-02-28 17:28:15] Reporting output tracks [FAILED] Error running /home/app/anaconda3/bin/tophat_reports --min-anchor 8 --splice-mismatches 0 --min-report-intron 50 --max-report-intron 100000 --min-isoform-fraction 0.15 --output-dir Glentis/ --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 100000 --read-mismatches 2 --read-gap-length 2 --read-edit-dist 2 --read-realign-edit-dist 3 --max-insertion-length 3 --max-deletion-length 3 --bowtie1 --fusion-search --fusion-anchor-length 13 --fusion-min-dist 100000 --fusion-read-mismatches 2 --fusion-multireads 2 --fusion-multipairs 2 --fusion-ignore-chromosomes chrM -z gzip -p10 --inner-dist-mean 0 --inner-dist-std-dev 80 --no-closure-search --no-coverage-search --no-microexon-search --sam-header Glentis/tmp/hg19bt1_genome.bwt.samheader.sam --report-discordant-pair-alignments --report-mixed-alignments --samtools=/home/app/anaconda3/bin/samtools_0.1.18 --bowtie2-max-penalty 6 --bowtie2-min-penalty 2 --bowtie2-penalty-for-N 1 --bowtie2-read-gap-open 5 --bowtie2-read-gap-cont 3 --bowtie2-ref-gap-open 5 --bowtie2-ref-gap-cont 3 Glentis/tmp/hg19bt1.fa Glentis/junctions.bed Glentis/insertions.bed Glentis/deletions.bed Glentis/fusions.out Glentis/tmp/accepted_hits Glentis/tmp/left_kept_reads.mapped.bam,Glentis/tmp/left_kept_reads.candidates Glentis/tmp/left_kept_reads.bam Glentis/tmp/right_kept_reads.mapped.bam,Glentis/tmp/right_kept_reads.candidates Glentis/tmp/right_kept_reads.bam ./SeqAn-1.4.2/seqan/basic/basic_exception.h:236 FAILED! (Uncaught exception of type St12out_of_range: basic_string::substr)

Any suggestions ?

RNA-Seq • 1.4k views
ADD COMMENT
1
Entering edit mode

Hello dimitrischat,

Note that TopHat is not the most recommended tool for RNAseq experiment, take a look at HISAT2 or STAR

Issue similar to this one I guess : Tophat2 "error running tophat_reports"

ADD REPLY

Login before adding your answer.

Traffic: 1696 users visited in the last hour
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6