Hi,
I've got Illumina Paired-End reads (2x 150 in --fr orientation). I want to filter my .SAM/.BAM files based on average read quality. Does anyone know an easy to use tool (Preferable which can run via Java or Windows), which is able to discard reads when average quality is <20?
without checking the seqanswers links you can also go with trimmomatic or cutadapt for filter the fastq files before mapping (which also makes sense in terms of CPU-time....