Entering edit mode
8.9 years ago
sangita_b
▴
90
Hi,
I am repeating alignments using TopHat, I am using the same Bowtie index as I used previously (i.e I have successfully aligned reads using this index)
My command line is below:
tophat p 5 \
-G /home/msxakk/Desktop/NOT-BACKED-UP/iGenomes/Homo_sapiens/Ensembl/GRCh37/Annotation/Genes/genes.gtf \
-o 3a_q20 \
/home/msxakk/Desktop/NOT-BACKED-UP/iGenomes/Homo_sapiens/Ensembl/GRCh37/Sequence/Bowtie2Index/genome \
3aqtrimR1.fastq 3aqtrimR2.fastq
However the following error appears:
[2016-01-04 11:24:00] Beginning TopHat run (v2.0.12)
-----------------------------------------------
[2016-01-04 11:24:00] Checking for Bowtie
Bowtie version: 2.2.3.0
[2016-01-04 11:24:00] Checking for Samtools
Samtools version: 0.1.18.0
[2016-01-04 11:24:00] Checking for Bowtie index files (genome)..
Error: Could not find Bowtie 2 index files (p.*.bt2)
Can anyone shed light on why Bowtie cannot locate/ use the index files?
Thanks
Sangita
Any particular reason you're using a version of TopHat2 that's a year and a half old?
I trimmed my fastq files and noticed that when aligning these files the concordant alignment rate was 0.4% (for my other samples the alignment rate was 90-92%).
Long story short I am repeating the alignments and want to use the same version of TopHat that I used originally (I am worried that the trimming has affected the alignment).
Thanks