User Tools

Site Tools


population-diversity:microbiome-analysis-with-qiime2-using-illumina-paired-end-sequence-data

Differences

This shows you the differences between two versions of the page.

Link to this comparison view

Both sides previous revisionPrevious revision
Next revision
Previous revision
Next revisionBoth sides next revision
population-diversity:microbiome-analysis-with-qiime2-using-illumina-paired-end-sequence-data [2020/03/30 14:23] – [Importing data into Qiime2] bnginapopulation-diversity:microbiome-analysis-with-qiime2-using-illumina-paired-end-sequence-data [2020/04/29 13:17] – removed bngina
Line 1: Line 1:
-====== Analysis of Microbiome data ====== 
  
-Micriobial analysis aims to understand microbes and their functions in their environments. [[https://docs.qiime2.org/2020.2/tutorials/overview/| QIIME2]] (**Q**uantitative **I**nsights **I**nto **M**icrobial **E**cology) is a powerful, extensible, and decentralized microbiome analysis package with a focus on data and analysis transparency. QIIME 2 enables researchers to start an analysis with raw DNA sequence data and finish with publication-quality figures and statistical results. 
- 
-We outline a pipeline to analyse 16S/18S paired-end sequencing data. Qiime2 can be used to analyse single-end and paired-end data.  
- 
-==== Importing data into Qiime2 ==== 
- 
-[[https://docs.qiime2.org/2020.2/concepts/|Data]] used and produced by qiime2 are stored as artifacts. Artifacts contain data and metadata and have a ''.qza'' extension. Qiime2 provides methods to view information (data and metadata) stored in artifacts by creating visualizations, that have a ''.qzv'' extension.  
- 
-We import raw fastq files into qiime2. Depending on the sequencing platform used to generate the data, you will have data that has been de-multiplexed into sample specif fastq files, or not. The MiSeq platform at [[ https://hub.africabiosciences.org/| BecA-ILRI Hub]] will de-multiplex the data and we get sample specific fastq files. 
- 
-Read more about [[ https://docs.qiime2.org/2020.2/tutorials/importing/|different data types and importing them into qiime2]] for anlaysis. We will be importing data described as type //Cassava 1.8 paired-end de-multiplexed fastq//. 
- 
-To import fastq files; 
- 
-<code> 
- 
-#i create a directory to store all my artifact i.e '.qza' and the related visualization i.e '.qzv' files. 
- 
-mkdir /home/mydir/qiime2_data/ 
- 
-#import the fastq files 
- 
-qiime tools import \ 
- --type 'SampleData[PairedEndSequencesWithQuality]' \ 
- --input-path /home/mydir/qiime2_data/ \ 
- --input-format CasavaOneEightSingleLanePerSampleDirFmt \ 
- --output-path /home/mydir/qiime2_data/my_raw_data.qza 
-</code> 
- 
-We mentioned that qiime2 provides method to summarize and view artifacts by storing them as visualizations, .qzv, files. The ''.qzv''  files can be opened on any browser using [[https://view.qiime2.org/ |qiime viewer]]. To create visualization for the imported data; 
- 
-<code> 
- 
-qiime demux summarize \ 
- --i-data  /home/mydir/qiime2_data/my_raw_data.qza \ 
- --o-visualization /home/mydir/qiime2_data/my_raw_data.qzv 
-</code> 
population-diversity/microbiome-analysis-with-qiime2-using-illumina-paired-end-sequence-data.txt · Last modified: 2020/04/29 15:09 by bngina