Dear Galaxy users,
Does anyone know how to merge several FASTQ groomer files by using
Galaxy? If not, is there any other program that can achieve this? The size of
one FASTQ groomer file is around 1GB. Thank you!
Best regards,
Xiefan Fang, Ph.D.
Postdoctoral associate
Department of
Dear galaxy users,
I am trying to map some multiplexing bisulfite PCR data (Illumina) to
our 20+ genes of interest. I want to use the Map with Bowtie for Illumina in
Galaxy. Therefore, I need to change the reference genome to my known DNA
sequences. However, I don't know how to make such
2 matches
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