Excessive data loss after trimming
Hi everyone!
I am trimming the adapters of my data, for one of the controls cutadapt It's only keeping the 5.2% of the reads after trimming and removing reads shorter than 17bp
$ cutadapt -a GATCGGAAGAGCACACGTCTGAACTCCAGTCACATCACGATCTCGTATGCCGTCTTCTGCTTG -j 4 -m 17 -o control_2_trimmed.fastq control_2.fastq
=== Summary ===
Total reads processed: 5,252,641
Reads with adapters: 5,169,644 (98.4%)
Reads that were too short: 4,981,734 (94.8%)
Reads written (passing filters): 270,907 (5.2%)
Total basepairs processed: 262,632,050 bp
Total written (filtered): 8,801,796 bp (3.4%)
While for the other samples values around 40% are obtained. Is the problem somehow my foult or coud It be from the data?
Thank you in advance, Jose
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Looks to me like library prep was screwed up and you got primer dimer, can you get a hold on the library QC (pre-sequencing)? Maybe other people with some more experience can comment
Can you try removing minimum length filter
-m 17? Though it doesn't help much, but you would know number reads without any length filter in this file. As Asaf pointed, try reaching sequencing core @ jomagrax