Hi All,
I have raw paired-end fastqc files of read length (151 bases). I would like to trim off last 50 bases and would like to keep just 101 bases from each read. I used following command to perform the activity. Am I missing something or good to go?
Currently the program is running, I couldn't see the output. But I would like to about the parameters I have used.
java -jar trimmomatic-0.32.jar -threads 6 PE -phred33
S1_L001-L004_R1.all.fastq.gz S1_L001-L004_R2.all.fastq.gz
S1_L001-L004_R1.all.paired.trimmed.fastq.gz
S1_L001-L004_R1.all.unpaired.trimmed.fastq.gz
S1_L001-L004_R2.all.paired.trimmed.fastq.gz
S1_L001-L004_R2.all.unpaired.trimmed.fastq.gz
ILLUMINACLIP:Trimmomatic-0.32/adapters/Illumina-TruSeqAdapter.fa:2:30:10
ILLUMINACLIP:Trimmomatic-0.32/adapters/Illumina-MultiplexingPrimer.fa:2:30:10
CROP:101
LEADING:20
TRAILING:20
MINLEN:20
You should be able to look at the result file while the program is running (
zmore
orgzip -c filename | more
).Thanks for providing me the command.