# Biological screens from linear codes: theory and tools

**Authors:** Yaniv Erlich, Anna Gilbert, Hung Ngo, Atri Rudra, Nicolas Thierry-Mieg, Mary Wootters, Dina Zielinski, Or Zuk

bioRxiv · DOI: 10.1101/035352 · bioRxiv · 2015-01-01

## TL;DR

This paper introduces a new method using linear codes to efficiently design biological experiments that test many samples at once.

## Contribution

The paper introduces the use of Reed-Solomon and linear codes for efficient combinatorial pooling in biological screens.

## Key findings

- Reed-Solomon codes provide efficient and modular designs for biological pooling.
- The method reduces waste and increases efficiency in large-scale biological experiments.
- Tools are provided for constructing and executing pooling designs with strong guarantees.

## Abstract

Molecular biology increasingly relies on large screens where enormous numbers of specimens are systematically assayed in the search for a particular, rare outcome. These screens include the systematic testing of small molecules for potential drugs and testing the association between genetic variation and a phenotype of interest. While these screens are “hypothesis-free,” they can be wasteful; pooling the specimens and then testing the pools is more efficient. We articulate in precise mathematical ways the type of structures useful in combinatorial pooling designs so as to eliminate waste, to provide light weight, flexible, and modular designs. We show that Reed-Solomon codes, and more generally linear codes, satisfy all of these mathematical properties. We further demonstrate the power of this technique with Reed-Solomonbased biological experiments. We provide general purpose tools for experimentalists to construct and carry out practical pooling designs with rigorous guarantees for large screens.

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/10.1101/035352/full.md

## References

26 references — full list in the complete paper: https://tomesphere.com/paper/10.1101/035352/full.md

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Source: https://tomesphere.com/paper/10.1101/035352