Skip to content

Machine learning to distinguish two types of T-cell receptor subregions.

License

Notifications You must be signed in to change notification settings

sannpeterson/TumorSTOppy

 
 

Folders and files

NameName
Last commit message
Last commit date

Latest commit

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Repository files navigation

We designed a machine learning method to distinguish two types of T cell receptor hypervariable CDR3 sequences!

This particular region is of high interest in immunology because it is binding to antigens that are presented on the surface of human cells. This interaction will eventually trigger adaptive immune responses which eliminates the pathogens, such as virus infection, or sometimes cancer cells.
In order to understand which CDR3 sequences may bind to cancer antigens, we have prioritized 20,000 cancer-specific CDR3s, which may possess distinct biochemical features from the non-cancer CDR3s. Your task is to develop a predictor that is able to distinguish the cancer-specific CDR3s from non-cancer CDR3s. I have provided an amino acid index matrix, which contains 544 features for each of the 20 amino acid. This matrix may help you to convert the amino acid characters into continuous values, which will be much more straightforward to design predictors.

What is ?

Overview Diagram

How to use

TumorSTOp.py

Software Workflow Diagram

File structure diagram

Define paths, variable names, etc

Installing from Github

  1. git clone https://github.com/NCBI-Hackathons/<this software>.git
  2. Edit the configuration files as below
  3. sh server/<this software>.sh to test
  4. Add cron job as required (to execute .sh script)

Configuration

Examples here

Testing

We tested four different tools with . They can be found in server/tools/ .

About

Machine learning to distinguish two types of T-cell receptor subregions.

Topics

Resources

License

Stars

Watchers

Forks

Releases

No releases published

Packages

No packages published

Languages

  • Python 93.7%
  • HTML 6.3%