I see that BWA ALN has an -I flag for changing the quality of the reads. I don't see this option for BWA MEM? Does anyone know if I'm missing something?
You can use my reformat tool to change ASCII-64 qualities to ASCII-33 (and most other format conversions). It supports piping from stdin and to stdout, so you don't have to write a temp file. And it's the fastest format convert of which I am aware.
Hi, I just new to bioinformatics. I have some MGI single-ended NIPT sequencing, each fastq file contains multiple 50bp sequences after trimming. I have read …
Hi everyone, I'm sorry if it is answered anywhere else, I have raw dna-seq paired-end sequence reads data from different libraries of read length for …
<p>I want to switch from using <a href='http://bio-bwa.sourceforge.net/'>bwa</a> aln+sampe to <a href='http://bio-bwa.sourceforge.net/'>bwa</a>-mem, but I notice that there is no quality soft-trimming in the latter. (It …
What is the size of your reads ? See Heng's comment:Aligning Sequence Reads, Clone Sequences And Assembly Contigs With Bwa-Mem
BWA-MEM however lacks the following features:
100bp. I wanted to use mem for consistency across some simulations and real data.
Honestly, I was stuck between mem and aln for my 100bp data, and aln performed much better, more reads aligned.
You're not missing anything: Bwa Mem: How To Specify The Fastq Phred Format? (see my link to a bwa email list message about this from Heng Li).