I am dealing with some RNA-seq data. First, I assemblied the short reads to contigs using Trinity, and then map the short reads to the contigs using BWA. I would like to get ungapped alignment from BWA by setting -o to 0 and other parameters as default. However, I still got gapped alignment. So my question is: what parameter should I set to get ungapped alignment from BWA. Thanks in advance!
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by SEQadmin2
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