This repository hosts a ETL pipeline designed for a toy dataset mimicking a genomics dataset.

It transforms the dataset into an analysable format that enables easy querying for the discovery of overlaps between sequences.

When cleaning this data, a number of assumptions are made:

1. The id column has no significance beyond being a database id
2. Duplicate entries have no significance
3. Sequence-type pairs are unique
4. When there are two start events, the earliest location is true
5. Events of type unclear_read signal that this sequence-type exists at this location
6. If the start event is less than the end event, treat them in reverse

• Install Miniconda
• Create an environment conda create -n genomics_etl python=3.9 -y
• Activate your new environment conda activate genomics_etl
• Install this package in editable mode pip install -e .

To run the ETL pipeline with queries showing overlaps between sequence execute python genomics_etl/__init__.py from a terminal