Skip to content

Develop algorithms to classify genetic mutations based on clinical evidence (text).

Notifications You must be signed in to change notification settings

tbsraja/Personalized_Cancer_Treatment

Folders and files

NameName
Last commit message
Last commit date

Latest commit

 

History

4 Commits
 
 
 
 
 
 

Repository files navigation

Personalized Medicine: Redefining Cancer Treatment

Kaggle - Personalized Medicine: Redefining Cancer Treatment

Problem statement

In this problem we develop algorithms to classify genetic mutations based on clinical evidence (text).

Mapping real world problem to ML problem

  • There are nine different classes a genetic mutation can be classified on.
  • Multi-Class Classification problem

Business objectives

  • The cost of a mis-classification can be very high.
  • Provide the probability that each data-point belonging to each of the nine classes for better interpretation.
  • Interpretability is important. (Will be useful for Diagnosis)
  • No-strict latency requirements.

Performance metric

  • Cross entropy
  • Confusion matrix

Overview of the Data set

  • training_variants provides the information about the genetic mutations.
  • training_text provides the clinical evidence (text) that human experts used to classify the genetic mutations. Both are linked via the ID field.

training_variants

A comma separated file containing the description of the genetic mutations used for training.

  • ID : The id of the row used to link the mutation to the clinical evidence
  • Gene : The gene where this genetic mutation is located
  • Variation : The aminoacid change for this mutations
  • Class : The class (1-9) this genetic mutation has been classified into

training_text

A double pipe (||) delimited file that contains the clinical evidence (text) used to classify genetic mutations.

  • ID : the id of the row used to link the clinical evidence to the genetic mutation
  • Text : the clinical evidence used to classify the genetic mutation

Train-Test Split:

  • We build train and test by randomly splitting in the ratio of 70:30

About

Develop algorithms to classify genetic mutations based on clinical evidence (text).

Topics

Resources

Stars

Watchers

Forks

Releases

No releases published

Packages

No packages published