Thanks Devon,
Sorry
I placed the orf_coding.fasta (my reference genome) in the bowtie2 file and indexed the genome in the same bowtie2, and run this syntax but error,
May you please tell me a solution?
[izadi@lbox161 bowtie2-2.2.5]$ $TOP/tophat -r 20 orf_coding.fasta SRR1944914_trimmed.fastq SRR1944926_trimmed.fastq
[2015-09-01 10:27:50] Beginning TopHat run (v2.1.0)
-----------------------------------------------
[2015-09-01 10:27:50] Checking for Bowtie
Bowtie version: 2.2.5.0
[2015-09-01 10:27:50] Checking for Bowtie index files (genome)..
Error: Could not find Bowtie 2 index files (orf_coding.fasta.*.bt2)
[izadi@lbox161 bowtie2-2.2.5]$ $TOP/tophat -r 20 orf_coding.fasta SRR1944914_trimmed_unmapped.fastq SRR1944926_trimmed_unmapped.fastq
[2015-09-01 10:29:01] Beginning TopHat run (v2.1.0)
-----------------------------------------------
[2015-09-01 10:29:01] Checking for Bowtie
Bowtie version: 2.2.5.0
[2015-09-01 10:29:01] Checking for Bowtie index files (genome)..
Error: Could not find Bowtie 2 index files (orf_coding.fasta.*.bt2)
[izadi@lbox161 bowtie2-2.2.5]$
Run tophat on each sample separately (or write a simple bash script with a list of fastq file names as input and specify different output directory for each of them). In case of paired-end
reads_1.fqandreads_2.fqdefines for Right and Left.