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docs/index.html

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@@ -107,7 +107,7 @@ <h3 class="anchored" data-anchor-id="bioconductor">Bioconductor</h3>
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<ul>
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<li><a href="https://microbiome.github.io/outreach/intro.html" target="_blank">Intro</a></li>
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<li><a href="https://microbiome.github.io/outreach/bioconductor.html" target="_blank">Bioconductor project</a></li>
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<li><a href="https://microbiome.github.io/outreach/oma.html" target="_blank">Orchestrating microbiome Analysis with Bioconductor</a></li>
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<li><a href="https://microbiome.github.io/outreach/oma.html" target="_blank">Orchestrating Microbiome Analysis with Bioconductor</a></li>
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</ul>
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</section>
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<section id="quarto" class="level3">

docs/oma.html

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docs/quarto.html

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@@ -516,7 +516,7 @@ <h2>Example 2.3: YAML Parameters</h2>
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<p>editor: visual</p>
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<p>smaller: true</p>
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<p>author: Escherichia coli</p>
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<p>date: 2024-11-24</p>
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<p>date: 2024-11-27</p>
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<p><code>---</code></p>
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</section>
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<section id="exercise-2" class="slide level2">

docs/search.json

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quarto/oma.qmd

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- ~2,300 R packages
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- Review, testing, documentation
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- Genomics, transcriptomics, microbiomics, ...
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```{r}
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#| label: bioc_packages
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p1
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```
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## Data containers form the foundation {.smaller}
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## Data containers form the core {.smaller}
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```{r}
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#| label: data_container
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y = c(2, 1, 0), # Centers of ellipses
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a = c(4, 3, 2), # Widths of ellipses
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b = c(3, 2, 1), # Heights of ellipses
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label = c("COMMUNITY", "PACKAGES", "DATA"), # Labels for each ellipse
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label = c("COMMUNITY", "METHODS", "DATA CONTAINER"), # Labels for each ellipse
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label_y = c(4, 1.75, 0) # Adjusted vertical positions for labels
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)
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- Extension to SummarizedExperiment
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- Optimal for microbiome data
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- Links microbiome field to larger SE family
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- Links microbiome field to larger SummarizedExperiment family
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##
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![](images/SE.png){fig-alt="SummarizedExperiment class" fig-align="center" width=10%}
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## {transition="fade" transition-speed="slow"}
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##
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![](images/paste-14DB8F76.png){fig-alt="TreeSummarizedExperiment class" fig-align="center" width=10%}
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## MIcrobiome Analysis (mia) {transition="none"}
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## MIcrobiome Analysis (mia)
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```{r}
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#| label: mia_stats
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- Scalable & optimized for large datasets
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- Comprehensive documentation
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_Allows us to develop modular and efficient workflows_
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_Allows us to develop efficient microbiome data science workflows_
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## {auto-animate="true"}
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```r
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# Load package
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library(mia)
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# Load example dataset
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data("peerj13075")
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tse <- peerj13075
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```
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```{r}
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#| label: show_treese
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# Load package
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library(mia)
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# Load example dataset
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data("peerj13075")
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tse <- peerj13075
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tse
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```
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## {auto-animate="true"}
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```r
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# Agglomerate to genus level
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tse <- agglomerateByRank(tse, rank = "genus")
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```
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## {auto-animate="true"}
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```r
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# Agglomerate to genus level
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tse <- agglomerateByRank(tse, rank = "genus")
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# Add relative abundances
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tse <- transformAssay(tse, method = "relabundance")
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```
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```{r}
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#| label: show_transform
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# Agglomerate to genus level
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tse <- agglomerateByRank(tse, rank = "genus")
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# Add relative abundances
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tse <- transformAssay(tse, method = "relabundance")
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```
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## {auto-animate="true"}
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```r
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# Load visualization package
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library(miaViz)
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# Summarize abundance of top taxa
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plotAbundanceDensity(tse, assay.type = "relabundance")
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```
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```{r}
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#| label: show_prevalence
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# Load visualization package
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library(miaViz)
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# Summarize abundance of top taxa
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plotAbundanceDensity(tse, assay.type = "relabundance")
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```
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## {auto-animate="true"}
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```r
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# Calculate alpha diversity indices
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tse <- addAlpha(tse, index = "shannon")
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```
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## {auto-animate="true"}
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```r
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# Calculate alpha diversity indices
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tse <- addAlpha(tse, index = "shannon")
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# Load single-cell analysis package that has useful, complementary tools
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library(scater)
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# Plot alpha diversity
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plotColData(tse, x = "Geographical_location", y = "shannon")
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```
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```{r}
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#| label: show_alpha
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#| fig-height: 4
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# Calculate alpha diversity indices
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tse <- addAlpha(tse, index = "shannon")
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# Load single-cell analysis package that has useful, complementary tools
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library(scater)
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# Plot alpha diversity
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plotColData(tse, x = "Geographical_location", y = "shannon")
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```
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## {auto-animate="true"}
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```r
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# Perform PCoA
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tse <- runMDS(tse, assay.type = "relabundance", FUN = getDissimilarity, method = "bray")
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```
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## {auto-animate="true"}
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```r
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# Perform PCoA
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tse <- runMDS(tse, assay.type = "relabundance", FUN = getDissimilarity, method = "bray")
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# Plot PCoA
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plotReducedDim(tse, dimred = "MDS", colour_by = "Geographical_location")
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```
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```{r}
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#| label: show_pcoa
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# Perform PCoA
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tse <- runMDS(tse, assay.type = "relabundance", FUN = getDissimilarity, method = "bray")
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# Plot PCoA
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plotReducedDim(tse, dimred = "MDS", colour_by = "Geographical_location")
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```
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## Orchestrating Microbiome Analysis with Bioconductor
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[microbiome.github.io/OMA](https://microbiome.github.io/OMA/docs/devel/){preview-link="true"}
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:::
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## Summary
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## Poem of the day
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::: columns
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::: {.column width="60%"}
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_OMA’s guide will light the way,_
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_Helping you every step of the day._
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_helping you every step of the day._
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:::
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