Conrad S. Leonard

300 Herston Road
Brisbane, QLD, Australia

Last Updated: 09/26/2026

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Found 44 publications

Explainable machine learning identifies features and thresholds predictive of immunotherapy response.

Explainable machine learning identifies features and thresholds predictive of immunotherapy response.

Journal: Scientific reports
Published: October 17, 2025

Multi-omics reveals key molecular and cellular features of advanced small cell lung cancers associated with distinct therapeutic opportunities.

Multi-omics reveals key molecular and cellular features of advanced small cell lung cancers associated with distinct therapeutic opportunities.

Journal: Genome medicine
Published: October 11, 2025

Multiomic profiling of checkpoint inhibitor-treated melanoma: Identifying predictors of response and resistance, and markers of biological discordance.

Multiomic profiling of checkpoint inhibitor-treated melanoma: Identifying predictors of response and resistance, and markers of biological discordance.

Journal: Cancer cell
Published: February 07, 2025

Performance of somatic structural variant calling in lung cancer using Oxford Nanopore sequencing technology.

Performance of somatic structural variant calling in lung cancer using Oxford Nanopore sequencing technology.

Journal: BMC genomics
Published: March 01, 2024

Evaluation of Endobronchial Ultrasound-Guided Transbronchial Needle Aspiration (EBUS-TBNA) Samples from Advanced Non-Small Cell Lung Cancer for Whole Genome, Whole Exome and Comprehensive Panel Sequencing.

Evaluation of Endobronchial Ultrasound-Guided Transbronchial Needle Aspiration (EBUS-TBNA) Samples from Advanced Non-Small Cell Lung Cancer for Whole Genome, Whole Exome and Comprehensive Panel Sequencing.

Journal: Cancers
Published: December 22, 2023

streammd: fast low-memory duplicate marking using a Bloom filter.

streammd: fast low-memory duplicate marking using a Bloom filter.

Journal: Bioinformatics (Oxford, England)
Published: October 26, 2022

The clinical utility and costs of whole-genome sequencing to detect cancer susceptibility variants-a multi-site prospective cohort study.

The clinical utility and costs of whole-genome sequencing to detect cancer susceptibility variants-a multi-site prospective cohort study.

Journal: Genome medicine
Published: October 04, 2022

Comparative Genomics Provides Etiologic and Biological Insight into Melanoma Subtypes.

Comparative Genomics Provides Etiologic and Biological Insight into Melanoma Subtypes.

Journal: Cancer discovery
Published: May 24, 2022

Analysis of hereditary cancer gene variant classifications from ClinVar indicates a need for regular reassessment of clinical assertions.

Analysis of hereditary cancer gene variant classifications from ClinVar indicates a need for regular reassessment of clinical assertions.

Journal: Human mutation
Published: January 27, 2022

qmotif: determination of telomere content from whole-genome sequence data.

qmotif: determination of telomere content from whole-genome sequence data.

Journal: Bioinformatics advances
Published: November 17, 2021

Comparison of actionable events detected in cancer genomes by whole-genome sequencing, in silico whole-exome and mutation panels.

Comparison of actionable events detected in cancer genomes by whole-genome sequencing, in silico whole-exome and mutation panels.

Journal: ESMO open
Published: October 21, 2021

Multi-omic features of oesophageal adenocarcinoma in patients treated with preoperative neoadjuvant therapy.

Multi-omic features of oesophageal adenocarcinoma in patients treated with preoperative neoadjuvant therapy.

Journal: Nature communications
Published: August 25, 2021
Showing 1-12 of 44

Last Updated: 09/26/2026