Dear Experts !!
I want to use Galaxy to analyze Illumina 16S metagenome data, which is ~200 fastq files, paired-end reads (meaning 100 samples), in 2 groups.
Basically, I'd like to identify microorganims that are differentially abindant (?) in one of the 2 groups (healthy vs disease).
Since I am not good at all with Unix, I want to use galaxy on the web.
I can not find any recent Galaxy example/history/work-flow that starts from importing multi samples to the final analysis.
I am very new to NGS in general.
Would appreciate your advice.
I want to use Galaxy to analyze Illumina 16S metagenome data, which is ~200 fastq files, paired-end reads (meaning 100 samples), in 2 groups.
Basically, I'd like to identify microorganims that are differentially abindant (?) in one of the 2 groups (healthy vs disease).
Since I am not good at all with Unix, I want to use galaxy on the web.
I can not find any recent Galaxy example/history/work-flow that starts from importing multi samples to the final analysis.
I am very new to NGS in general.
Would appreciate your advice.
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