Do you have a preference on one tool over another?
Hello everyone,
I encountered small questions when analyzing AD patients' blood DNA NGS data. After mapping sequencing data to hg19 genome, I want mapping the remaining unmapped reads to viral genome. I found viral genome reference on ftp://ftp.ncbi.nlm.nih.gov/refseq/release/viral/, but there are 3 files (viral.1.1.genomic.fna.gz, viral.2.1.genomic.fna.gz, viral.3.1.genomic.fna.gz).
I merged these 3 files and using blast to mapping unmapped reads to the reference. Is it right?
The mapping is so slow(20 cores dealing with 20000000 reads). Does anyone knows any methods to do this faster?
Thanks!!!
1 answer
Looks like you're looking for a metagenomics tool - tools like Kraken 2 or Centrifuge are much faster for what you want to do
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Blast is not the right tool for doing this. You should switch back to an NGS data aligner.