物种分类

第一步，下载注释
看官方文档的介绍

We’ll do that using a pre-trained Naive Bayes classifier and the q2-feature-classifier plugin. This classifier was trained on the Greengenes 13_8 99% OTUs, where the sequences have been trimmed to only include 250 bases from the region of the 16S that was sequenced in this analysis (the V4 region, bound by the 515F/806R primer pair).

注意了，这里说明了用这种注释的前提条件，因为不是所有实验条件都一样的
比如我的材料就不是用 V4 区域，所以要自己制作一个qiime2 的classifier
文档里面的NOTE也提到了

Taxonomic classifiers perform best when they are trained based on your specific sample preparation and sequencing parameters, including the primers that were used for amplification and the length of your sequence reads. Therefore in general you should follow the instructions in Training feature classifiers with q2-feature-classifier to train your own taxonomic classifiers. We provide some common classifiers on our data resources page, including Silva-based 16S classifiers, though in the future we may stop providing these in favor of having users train their own classifiers which will be most relevant to their sequence data.

我自己下载train了一个

自己的classifier

接着做

官网代码

qiime feature-classifier classify-sklearn \  --i-classifier gg-13-8-99-515-806-nb-classifier.qza \  --i-reads rep-seqs.qza \  --o-classification taxonomy.qzaqiime metadata tabulate \  --m-input-file taxonomy.qza \  --o-visualization taxonomy.qzv

qiime taxa barplot \  --i-table table.qza \  --i-taxonomy taxonomy.qza \  --m-metadata-file sample-metadata.tsv \  --o-visualization taxa-bar-plots.qzv

基本上也是按照流程跑

最后得到物种分类柱状图

Differential abundance testing with ANCOM

差异丰度分析

We’ll start by creating a feature table that contains only the gut samples

qiime feature-table filter-samples \  --i-table table.qza \  --m-metadata-file sample-metadata.tsv \  --p-where "BodySite='gut'" \  --o-filtered-table gut-table.qza

ANCOM不允许有零

ANCOM operates on a FeatureTable[Composition] QIIME 2 artifact, which is based on frequencies of features on a per-sample basis, but cannot tolerate frequencies of zero.

所以要

qiime composition add-pseudocount \  --i-table gut-table.qza \  --o-composition-table comp-gut-table.qza

然后我们取subject 分组进行差异统计

We can then run ANCOM on the Subject column to determine what features differ in abundance across the gut samples of the two subjects.

qiime composition ancom \  --i-table comp-gut-table.qza \  --m-metadata-file sample-metadata.tsv \  --m-metadata-column Subject \  --o-visualization ancom-Subject.qzv

按照不同的水平分析

We’re also often interested in performing a differential abundance test at a specific taxonomic level. To do this, we can collapse the features in our FeatureTable[Frequency] at the taxonomic level of interest, and then re-run the above steps. In this tutorial, we collapse our feature table at the genus level (i.e. level 6 of the Greengenes taxonomy).

qiime taxa collapse \  --i-table gut-table.qza \  --i-taxonomy taxonomy.qza \  --p-level 6 \  --o-collapsed-table gut-table-l6.qzaqiime composition add-pseudocount \  --i-table gut-table-l6.qza \  --o-composition-table comp-gut-table-l6.qzaqiime composition ancom \  --i-table comp-gut-table-l6.qza \  --m-metadata-file sample-metadata.tsv \  --m-metadata-column Subject \  --o-visualization l6-ancom-Subject.qzv

一步到位，这里的p-level就是可以设置的水平参数

接下来就得到各种分析结果

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