Closed y-mone closed 8 years ago
Hi, I assume that your file with right mates and the file with left mates contains the same number of reads and the reads are in the same order in both files.
Then you can just run Kaiju twice and combine the output of both runs.
First, run Kaiju with the intact read pairs in paired-end mode:
kaiju -i leftmates.fastq -j rightmates.fastq -o pairedreads.out ...
Second, run the singletons:
kaiju -i singletons.fastq -o singletons.out ...
Then just concatenate them
cat pairedreads.out singletons.out > combined.out
Now you can run kaijuReport
or kaiju2krona
etc on the combined.out
file.
Hi, I want to analyse a set of reads with Kaiju. After the trimming step of my paired-end data, a part of the reads lost their mates and I obtain a fastq file with the right mate, a fastq file with the left mate and a fastq file with singletons. Please, could you tell me if is it possible to include all the reads (paired and singleton) in the kaiju analysis ?
Thank you in advance for your reply,