TARGET-SL: precision essential gene prediction using driver prioritisation and synthetic lethality

The ability to identify patient-specific vulnerabilities to guide cancer treatments is a vital area of research. However, predictive bioinformatics tools are difficult to translate into clinical applications due to a lack of in vitro and in vivo validation. While the increasing number of personalised driver prioritisation algorithms (PDPAs) report powerful patient-specific information, the results do not easily translate into treatment strategies. Critical in addressing this gap is the ability to meaningfully benchmark and validate PDPA predictions. To address this, we developed Tumour-specific Algorithm for Ranking GEnetic Targets via Synthetic Lethality (TARGET-SL), which utilises PDPA predictions to produce a ranked list of predicted essential genes that can be validated in vitro and in vivo. This framework employs a novel strategy to benchmark PDPAs, by comparing predictions with ground truth gene essentiality data from large-scale CRISPR-knockout and drug sensitivity screens. Importantly TARGET-SL identifies vulnerabilities that are more exclusive to individual tumours than predictions based on canonical driver genes. We further find that TARGET-SL is better at identifying sample-specific vulnerabilities than other similar tools.

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Publication Details

Journal
Briefings in Bioinformatics
Published
2025-05-01
DOI
https://doi.org/10.1093/bib/bbaf255
Citations
1
Primary Topic
CRISPR and Genetic Engineering
Type
article
Field-Weighted Citation Impact
0.81

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article

TARGET-SL: precision essential gene prediction using driver prioritisation and synthetic lethality

Matthew A. Field, Lionel Hebbard, Ulf Schmitz, Rhys Gillman
1 citations
Briefings in Bioinformatics
CRISPR and Genetic Engineering
0.81
article

TARGET-SL: precision essential gene prediction using driver prioritisation and synthetic lethality

Matthew A. Field, Lionel Hebbard, Ulf Schmitz, Rhys Gillman
article en
1 citations

Abstract

The ability to identify patient-specific vulnerabilities to guide cancer treatments is a vital area of research. However, predictive bioinformatics tools are difficult to translate into clinical applications due to a lack of in vitro and in vivo validation. While the increasing number of personalised driver prioritisation algorithms (PDPAs) report powerful patient-specific information, the results do not easily translate into treatment strategies. Critical in addressing this gap is the ability to meaningfully benchmark and validate PDPA predictions. To address this, we developed Tumour-specific Algorithm for Ranking GEnetic Targets via Synthetic Lethality (TARGET-SL), which utilises PDPA predictions to produce a ranked list of predicted essential genes that can be validated in vitro and in vivo. This framework employs a novel strategy to benchmark PDPAs, by comparing predictions with ground truth gene essentiality data from large-scale CRISPR-knockout and drug sensitivity screens. Importantly TARGET-SL identifies vulnerabilities that are more exclusive to individual tumours than predictions based on canonical driver genes. We further find that TARGET-SL is better at identifying sample-specific vulnerabilities than other similar tools.

Briefings in BioinformaticsVol. 26(3)
The University of Sydney (AU), Garvan Institute of Medical Research (AU), Australian Institute of Tropical Health and Medicine (AU), Westmead Hospital (AU), Charles Darwin University (AU), Menzies School of Health Research (AU), Westmead Institute (AU), Westmead Institute for Medical Research (AU), James Cook University (AU)
James Cook University, Tour de Cure, Medical Research Council, National Health and Medical Research Council, Cancer Council NSW
Good health and well-being
Openalex Percentile: Top 27%
CRISPR and Genetic Engineering
0.81
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