I have single end fastq file of metagenomics data. Can any one help me how to proceed with the data analysis of this data ? I have soil samples and I want to perform OTU, alpha diversity and Beta Diversity analysis on my data..!!
I have single end fastq file of metagenomics data. Can any one help me how to proceed with the data analysis of this data ? I have soil samples and I want to perform OTU, alpha diversity and Beta Diversity analysis on my data..!!
Have you looked at Qiime tutorials ( http://qiime.org/tutorials/processing_illumina_data.html )?
What exactly do you find too complex? The technical details of how to run the tool? Or its application, i.e. why you need to do certain processing steps? If the latter case is true, I recommend you modify your question to something like "Advice for useful introductory material on metagenomics analyses" or the like including a description of your background, i.e. what you already know about NGS data processing in general.
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See this post, it looks useful.
When paired end reads doesn't join, can i consider them single-end in metagenomic analysis?
@natasha.sernova The link is not related to my query. I have single end fastq file and the link you referred to is focused on merging pair-end files
Can you elaborate and mention specific questions you have? What's the biological question of interest that you have? And what do you already know about general metagenomics data processing?