Hello,
I noticed some reads had no quality score in my bam files generated with lra. (278604 out of 2.7 millions reads).
I wonder why ?
My bam were generated as follow:
zcat $FASTQ | lra align -ONT -t 24 $REF - -p s | samtools sort -@ 14 -o $BAM
samtools index $BAM -@ 34
Thank you!