Open EricSHo opened 4 years ago
Hi,
This feature is not available in CircMiner at the moment. It's a good idea to add it in the next versions of the software. However, the best solution will be to use a quality control pipeline to remove the problematic reads from the input data and then feed it to CircMiner.
Hi,
circminer detected there was a bad read in the fastq file (It's correct. I checked the fastq file) and aborted. Are there options I can set to bypass the abortion? It makes more sense to me to discard bad reads and move on.
Here's the error message: ERROR: read: ST-E00167:388:HCKK2ALXX:3:2115:30472:38948, length of sequence (136) does not match with quality (127)! Aborting
CircMiner 0.3.1
circminer --thread 3 \ --verbose 2 \ --gtf ../mm10/gencode.vM24.annotation.gtf \ --reference ../mm10/GRCm38.primary_assembly.genome.fa \ --seq1 ../fastq_dir/Mouse_F950-L${seqno}_good_1.fq.gz \ --seq2 ../fastq_dir/Mouse_F950-L${seqno}_good_2.fq.gz \ --output ${prefix}_circminer \ --scan-lev 2 \ --rlen 150 \ --sam
Your help is appreciated.
Thanks again.
Eric.