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Quantitative Comparison of Enrichment from DNA-Encoded Chemical Library Selections
Author(s) -
John C. Faver,
Kevin Riehle,
David R. Lancia,
Jared B. J. Milbank,
Christopher S. Kollmann,
Nicholas Simmons,
Zhifeng Yu,
Martin M. Matzuk
Publication year - 2019
Publication title -
acs combinatorial science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.928
H-Index - 81
eISSN - 2156-8952
pISSN - 2156-8944
DOI - 10.1021/acscombsci.8b00116
Subject(s) - computational biology , metric (unit) , selection (genetic algorithm) , dna sequencing , chemical library , dna , chemistry , drug discovery , computer science , biology , small molecule , machine learning , biochemistry , operations management , economics
DNA-encoded chemical libraries (DELs) provide a high-throughput and cost-effective route for screening billions of unique molecules for binding affinity for diverse protein targets. Identifying candidate compounds from these libraries involves affinity selection, DNA sequencing, and measuring enrichment in a sample pool of DNA barcodes. Successful detection of potent binders is affected by many factors, including selection parameters, chemical yields, library amplification, sequencing depth, sequencing errors, library sizes, and the chosen enrichment metric. To date, there has not been a clear consensus about how enrichment from DEL selections should be measured or reported. We propose a normalized  z-score enrichment metric using a binomial distribution model that satisfies important criteria that are relevant for analysis of DEL selection data. The introduced metric is robust with respect to library diversity and sampling and allows for quantitative comparisons of enrichment of n-synthons from parallel DEL selections. These features enable a comparative enrichment analysis strategy that can provide valuable information about hit compounds in early stage drug discovery.

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