library(tidyverse)
diff --git a/omics/data/betsy/meta_data.txt b/omics/data/betsy/meta_data.txt deleted file mode 100644 index fb451e7..0000000 --- a/omics/data/betsy/meta_data.txt +++ /dev/null @@ -1,19 +0,0 @@ -sample_id stage treatment sibling_rep -S14_C_5 stage_14 control five -S14_C_6 stage_14 control six -S14_C_A stage_14 control A -S14_F_5 stage_14 FGF five -S14_F_6 stage_14 FGF six -S14_F_A stage_14 FGF A -S20_C_5 stage_20 control five -S20_C_6 stage_20 control six -S20_C_A stage_20 control A -S20_F_5 stage_20 FGF five -S20_F_6 stage_20 FGF six -S20_F_A stage_20 FGF A -S30_C_5 stage_30 control five -S30_C_6 stage_30 control six -S30_C_A stage_30 control A -S30_F_5 stage_30 FGF five -S30_F_6 stage_30 FGF six -S30_F_A stage_30 FGF A diff --git a/omics/omics.html b/omics/omics.html index 6057230..3443d78 100644 --- a/omics/omics.html +++ b/omics/omics.html @@ -129,7 +129,7 @@
In this workshop you will
-tidyverse_conflicts() ──
-✖ dplyr::filter() masks stats::filter()
-✖ dplyr::lag() masks stats::lag()
-ℹ Use the conflicted package to force all conflicts to become errors
See later workshops.
data-raw
workshop-1.R
to carry out the rest of the work.tidyverse
Frog development: meta_data.txt
sample_id | -stage | -treatment | -sibling_rep | -
---|---|---|---|
S14_C_5 | -stage_14 | -control | -five | -
S14_C_6 | -stage_14 | -control | -six | -
S14_C_A | -stage_14 | -control | -A | -
S14_F_5 | -stage_14 | -FGF | -five | -
S14_F_6 | -stage_14 | -FGF | -six | -
S14_F_A | -stage_14 | -FGF | -A | -
S20_C_5 | -stage_20 | -control | -five | -
S20_C_6 | -stage_20 | -control | -six | -
S20_C_A | -stage_20 | -control | -A | -
S20_F_5 | -stage_20 | -FGF | -five | -
S20_F_6 | -stage_20 | -FGF | -six | -
S20_F_A | -stage_20 | -FGF | -A | -
S30_C_5 | -stage_30 | -control | -five | -
S30_C_6 | -stage_30 | -control | -six | -
S30_C_A | -stage_30 | -control | -A | -
S30_F_5 | -stage_30 | -FGF | -five | -
S30_F_6 | -stage_30 | -FGF | -six | -
S30_F_A | -stage_30 | -FGF | -A | -
The workshops will examine the “least interesting”: - the difference between the control and the FGF treated sibling at S30 - the difference between HSPC and Prog cells
+🐸 Frog development data - xlaevis_counts_S14.csv - xlaevis_counts_S20.csv - xlaevis_counts_S30.csv - meta_data.txt
+🐭 Stem cell data - surfaceome_hspc.csv - surfaceome_prog.csv - surfaceome_lthsc.csv
data-raw
open in understanding the data numbers of variables, organisation
🎬 Import xlaevis_counts_S30.csv, surfaceome_hspc.csv and surfaceome_prog.csv
The
+Distributions
🐸 Frog development data - 🎬 Make a script file called cont-fgf-s30.R
. This will a be commented analysis of the control vs FGF at S30 comparison. You will build on this each workshop and be able to use it as a template to examine other comparisons. Copy in the appropriate code and comments from workshop-1.R
. Edit to improve your comments where your understanding has developed since you made them.
🐭 Stem cell data - 🎬 Save the files to data-raw
🎬
You’re finished!