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Thread | Thread Starter | Forum | Replies | Last Post |
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#1 |
Junior Member
Location: Turkey Join Date: Jan 2019
Posts: 3
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Hello guys, a newbie in here.
I have reads from nanopore, converted fast5 files into fastq, what i am trying to do is extract the sequences between the primers. I attempt to do it by bbduk from BBMap. First I tried this Code:
./bbduk.sh in=/home/celik/Downloads/deneme/2/first0.fastq out=/home/dnacoder/Downloads/deneme/2/cikis.fasta literal=AGAGTTTGATCCTGGCTCAG,CTACGGCTACCTTGTTACGA Then I searched and tried this running this code Code:
java -ea -Xmx1g -cp /home/celik/Downloads/BBMAP/BBMap-master/sh/current/jgi.BBDuKF in=first0.fastq out=cikis.fastq literal=AGAGTTTGATCCTGGCTCAG,CTACGGCTACCTTGTTACGA Can anyone tell me what am I doing wrong, i ve looked on google and tried couple of things such as "export CLASSPATH=$CLASSPATH:." but did not make any change. Thanks in advance. |
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#2 |
Senior Member
Location: East Coast USA Join Date: Feb 2008
Posts: 7,092
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Are you doing this on windows? You have not moved any of the contents of BBMap software folder after you downloaded it?
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#3 |
Junior Member
Location: Turkey Join Date: Jan 2019
Posts: 3
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#4 |
Junior Member
Location: Turkey Join Date: Jan 2019
Posts: 3
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Guys anyone can help me? I am still struggling with this.
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Tags |
bbduk, bbmap, filter by primers |
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