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Merge pull request #22 from hds-sandbox/albarema-patch-1
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test yaml output
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albarema authored Dec 20, 2024
2 parents 3dd596e + 9cb790c commit 2411c7c
Showing 1 changed file with 13 additions and 11 deletions.
24 changes: 13 additions & 11 deletions Notebooks/05b_count_matrix.Rmd
Original file line number Diff line number Diff line change
Expand Up @@ -7,15 +7,15 @@ knit: (function(inputFile, encoding) {
encoding=encoding,
output_format='all',
output_dir='./')})
output:
html_document:
theme: yeti # nice theme for the webpage
toc: true # table of contents
toc_float: true # table of contents "floats" in the document
code_folding: show
collapse: false
df_print: paged # data frames are interactive
dev: png # what format do you want for the figures?
#output:
# html_document:
# theme: yeti # nice theme for the webpage
# toc: true # table of contents
# toc_float: true # table of contents "floats" in the document
# code_folding: show
# collapse: false
# df_print: paged # data frames are interactive
# dev: png # what format do you want for the figures?
---

```{r knitr, include = FALSE}
Expand Down Expand Up @@ -43,7 +43,9 @@ Approximate time: 20 minutes

For this analysis we will be using several R packages, some which have been installed from CRAN and others from Bioconductor. To use these packages (and the functions contained within them), we need to **load the libraries.**

```{r, echo=TRUE}
```{r}
#| echo: true
library(tidyverse)
library(DESeq2)
library(tximport)
Expand Down Expand Up @@ -170,7 +172,7 @@ To determine the appropriate statistical model, we need information about the di
pdata <- data %>%
gather(key = Sample, value = Count)
pdata
head(pdata)
```

And we plot our count distribution using all our samples:
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