diff --git a/README.md b/README.md
index 06f6cbe..b7476b1 100644
--- a/README.md
+++ b/README.md
@@ -14,7 +14,7 @@
Streamlit app (see GIF -->) to automate the creation of these plots with Python.
At the end of the project, we were able to identify less than 10 gene pairs showing the behavior of interest. That
information was used in combination with other data from different techniques (in silico and in vitro) to prioritize
- further studies evaluating the effect of inhibtion of those genes in cancer cell models.
+ further studies evaluating the effect of inhibtion of those genes in cancer cell models.
To see in full screen, right click on image and select "Open in new tab"
Problem
@@ -53,11 +52,11 @@NOTE: I am not planning on deploying my app to any server, it runs locally and I also set it up in Github Codespaces to share with others (see last section).
+NOTE: I am not planning on deploying my app to a hosted server (for now), it runs locally or in Github Codespaces (see last section).
Read the instructions and watch another demo of the Streamlit app here: Demo_KM_plotter
@@ -130,7 +129,7 @@ to the root directory for that experimental group to find the pairs of images to insert.NOTE: I am not planning on deploying my app to any server, it runs locally and I also set it up in Github Codespaces to share with others (see last section).
+NOTE: I am not planning on deploying my app to a hosted server (for now), it runs locally or in Github Codespaces (see last section).
Read the instructions and watch another demo of the Streamlit app here: Demo_PPTX_PLA
Summary
-Some summary here. +
During my graduate studies, I came across the Cancer Cell Line
+ Encyclopedia, which is a project containing information on over 1,800 cell models, including RNA
+ Seq gene expression data. Although my reseach group does not specialize in bioinfomatics, we used the CCLE dataset at times to
+ cross-validate some observations, potential gene candidates, or to look for cell model options we didn't have in-house.
+ I downloaded the 2019 dataset and noticed it was very large (around 1,800 by 20,000), and we only used a few cell
+ lines in our analyses. Moreover, we wanted different combinations of these cell lines per file, so I created a basic tool as a
+ Google Colab notebook (View tool)
+ to search and retrieve only the cell lines of interest.
+ However, I noticed that the dataset was merged with the Achilles project to make the DepMap project,
+ which added few more cell lines and several more datasets from other types of genomics, proteomics, and metabolomics assays. They also
+ reshaped datasets, reassigned IDs to make all datasets consistent, etc. Once I noticed the new version, I adapted my tool to work for the
+ new dataset (at that time, 23Q2), and generated a similar notebook.
+ Finally, when I discovered Streamlit the first data app I built attempted to replicate my tool for DepMap. I soon
+ discovered how easy was to add widgets and interactive plots that would allow not only to extract the data, but also to automate
+ basic data exploration and visualization of the cell lines and gene expression in a very user-friendly manner.
Problem
Solution
NOTE: I am not planning on deploying my app to any server, it runs locally and I also set it up in Github Codespaces to share with others (see last section).
+NOTE: I am not planning on deploying my app to a hosted server (for now), it runs locally or in Github Codespaces (see last section).
Read the instructions and watch another demo of the Streamlit app here: Demo_RNA_DepMap
@@ -199,7 +224,7 @@ If you have a Github account, you can create a Github Codespace with all the requirements to
run my apps. You only have to log into you account, click on the button below, create your Codespace (we all have 60h of
free usage per month!), and follow the instructions in this video→.
- ***Note that due to size limits, I did everything quickly but added notes so pause, read and see where I clicked!