It's creating only 1 output file. (actually, it's rewriting the same output file for every input file)
How can I run a same command in mac terminal for multiple files in a folder?
How can I run the same command in mac terminal for multiple files in a folder? The files are named like 24538_7#1_paired1.fq, 24538_7#1_paired2.fq, 24538_7#2_paired1.fq, 24538_7#2_paired2.fq, 24538_7#3_paired1.fq, 24538_7#3_paired2.fq, and so on.
The command is:
STAR --runThreadN 12 --genomeDir indices/STAR --twopassMode Basic --readFilesIn data/24538_7#1_paired1.fq data/24538_7#1_paired2.fq --outFileNamePrefix results/STAR/
Since filename involves a counter, so, obviously the filenames need to be changed.
I was trying to write command, but it's giving segmentation fault. My effort for the command is below:
for file in 24538_7#*.fq; do STAR --runThreadN 12 --genomeDir indices/STAR --twopassMode Basic --readFilesIn data/"${file%.fq}_paired1.fq" data/"${file%.fq}_paired2.fq" --outFileNamePrefix results/STAR/ ; done
(PS- I use MacOS)
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This looks correct. Remove the word echo when ready to run.
for file in 24538_7#*paired1.fq; do echo STAR --runThreadN 12 --genomeDir indices/STAR --twopassMode Basic --readFilesIn data/"${file%%_paired1.fq}_paired1.fq" data/"${file%%_paired1.fq}_paired2.fq" --outFileNamePrefix results/STAR/ ; done
STAR --runThreadN 12 --genomeDir indices/STAR --twopassMode Basic --readFilesIn data/24538_7#1_paired1.fq data/24538_7#1_paired2.fq --outFileNamePrefix results/STAR/
STAR --runThreadN 12 --genomeDir indices/STAR --twopassMode Basic --readFilesIn data/24538_7#2_paired1.fq data/24538_7#2_paired2.fq --outFileNamePrefix results/STAR/
STAR --runThreadN 12 --genomeDir indices/STAR --twopassMode Basic --readFilesIn data/24538_7#3_paired1.fq data/24538_7#3_paired2.fq --outFileNamePrefix results/STAR/
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For an idea of how you can get unique names for the output. Modify the last part as needed.
for file in 24538_7#*paired1.fq; do echo STAR --runThreadN 12 --genomeDir indices/STAR --twopassMode Basic --readFilesIn data/"${file%%_paired1.fq}_paired1.fq" data/"${file%%_paired1.fq}_paired2.fq" --outFileNamePrefix results/STAR/${file%%_paired1.fq}.STAR ; done
STAR --runThreadN 12 --genomeDir indices/STAR --twopassMode Basic --readFilesIn data/24538_7#1_paired1.fq data/24538_7#1_paired2.fq --outFileNamePrefix results/STAR/24538_7#1.STAR
STAR --runThreadN 12 --genomeDir indices/STAR --twopassMode Basic --readFilesIn data/24538_7#2_paired1.fq data/24538_7#2_paired2.fq --outFileNamePrefix results/STAR/24538_7#2.STAR
STAR --runThreadN 12 --genomeDir indices/STAR --twopassMode Basic --readFilesIn data/24538_7#3_paired1.fq data/24538_7#3_paired2.fq --outFileNamePrefix results/STAR/24538_7#3.STAR
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What genome are you aligning against? STAR requires at least 30+G of free RAM (for human sized genomes) so unless you have that available that may be your first problem.
Mouse genome. RAM isn't an issue for me. I've got a RAM 64 GB desktop(Mac- currently in use) and a 192 GB RAM Workstation Dell (in-store).