Entering edit mode
6.1 years ago
valizad2
▴
20
Hi all,
I am really having trouble doing the alignment in STAR using gff file. I tried downloading gtf files but I think finding and getting the files into cluster from Ensembl and USCS was very confusing. I was able to easily download gff files from NCBI but then using it in STAR is more complicated. I know I have to specify extra parameter for gff files and here is the code I am using:
STAR --runThreadN 12 --runMode genomeGenerate \
--genomeDir /home/n-z/valizad2/Sepsis_RNAseq/HumanData/GenomeDirectory \
--limitGenomeGenerateRAM 206609344554 \
--genomeFastaFiles GCF_000001405.38_GRCh38.p12_genomic.fna \
sjdbGTFtagExonParentTranscript Parent \
--sjdbGTFfile GCF_000001405.38_GRCh38.p12_genomic.gff \
--sjdbOverhang 100
Adding sjdbGTFtagExonParentTranscript Parent gives me the error below:
EXITING: FATAL INPUT ERROR: empty value for parameter "sjdbGTFtagExonParentTranscript Parent" in input "Command-Line-Initial" SOLUTION: use non-empty value for this parameter
I don't know why it's telling me the parameter is empty. I would appreciate your help.
Thanks!
Did you really run the command with
sjdbGTFtagExonParentTranscript Parent
, instead of--sjdbGTFtagExonParentTranscript Parent
?Yes, that was my mistake! Sorry. I ended up having to download the gtf files because I see in several places that using gff for gene counting is not a good idea.
Do you happen to know why I might have gotten this error when generating the index file using the gtf file?
Segmentation fault?
Hi valizad2, please:
1) use the code button to format your post
2) do not post questions as answers, either open a new question, or post as a comment to my comment above, or edit your question.
I fixed for you this time.
Sure, Thanks! Sorry about that.
Try not to mention RAM allocation or check your space. I hope in this way. Thanks