Skip to content
This repository was archived by the owner on May 29, 2019. It is now read-only.

az7jh2/Using-DeepDive-for-Gene-Variation-Inference

Repository files navigation

Using DeepDive for Gene Variation Inference

Another Natural Language Processing (NLP) exploration in Bioinformatic literatures in 2017 autumn semester. The previous exploration in 2016 autumn could refer here.

This is a Neural Information Processing Systems (NIPS) 2017 Competition Track named "Classifying Clinically Actionable Genetic Mutations", which was hosted by Kaggle.

To predict the effect of Genetic Variants to enable Personalized Medicine, we need to determine oncogenicity (4 classes) and mutation effect (9 classes) of the genes based on abstracts of biomedical literatures. It can be defined as a knowledge discovery task, i.e. gene-variation-effect relationship. I tried DeepDive, which has been stopped updating from 2017.

The detailed procedures could refer ppt file.

In this work, other skills were also needed:

  • A special program language DDlog presented by author
  • Other programming skills: bash, Python, SQL, HTML
  • A database tool PostgreSQL

About

Using DeepDive (An information Extraction Tool) to infer relationship of genes and variations from manually annotated literatures in a NIPS 2017 Competition.

Resources

License

Stars

Watchers

Forks

Releases

No releases published

Packages

 
 
 

Contributors