I am newbie to this (I started a week ago) Can you give me an example how to use this?
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Hello everyone,
Using this command tophat -p 8 -G genes.gtf -o c1_R1_thout genome SRR121576.fq SRR121577.fq I got this error:
[2014-08-14 14:49:06] Beginning TopHat run (v2.0.9)
-----------------------------------------------
[2014-08-14 14:49:06] Checking for Bowtie
Bowtie version: 2.1.0.0
[2014-08-14 14:49:06] Checking for Samtools
Samtools version: 0.1.19.0
[2014-08-14 14:49:06] Checking for Bowtie index files (genome)..
[2014-08-14 14:49:06] Checking for reference FASTA file
[2014-08-14 14:49:06] Generating SAM header for genome
format: fastq
quality scale: phred33 (default)
[2014-08-14 14:50:19] Reading known junctions from GTF file
[2014-08-14 14:50:22] Preparing reads
[FAILED]
Error running 'prep_reads'
terminate called after throwing an instance of 'int'
I cannot figure out what it's going wrong here. Any thoughts?
Thank you.
The "throwing an instance of 'int'" error is because these are colorspace files rather than regular fastq files. You'll need the --bowtie1 option as well as -C. You'll also need to use a colorspace index.
I am newbie to this (I started a week ago) Can you give me an example how to use this?
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Aside from the error, aligning two separate single-end libraries as though they were paired-end can also cause problems. You wanted to execute
tophat -p 8 -G genes.gtf -o c1_R1_thout genome SRR121576.fq,SRR121577.fqor something like that.Normally I wanted to execute CD4 and CD8 cells rna-seq data cd4 has one fastq file but CD8 has 3 so I think to execute codes like this order;
Then
cuffmergeit. Is it wrong?That's wrong. What you want is:
You don't have paired-end reads, so you'll just get wrong results doing what you wrote.
When I tried that command it just gave me TopHat index.
Oops! I forgot "genome". I updated that comment.
I still get the "terminate called after throwing an instance of 'int'" error
Yeah, that's its own cryptic problem. Often this means a Phred score is out of range.