Claude Chelala

This study benchmarks three low-input whole exome sequencing workflows for ctDNA profiling in PDAC, showing Agilent V8 provides best performance in low-input settings.

This study identifies CoAsy as a regulator of HIF signalling in TNBC, showing its loss stabilizes HIF-1 and HIF-2 and correlates with poor patient outcomes.

This study examines breast cancer differences between African, South Asian, and European ancestries, finding earlier onset, different tumor characteristics, and varied mutation patterns.

SNPnexus COVID provides a web-based platform for analyzing genetic variants in COVID-19 patient genomes to prioritize clinically relevant variants for prevention and treatment.

IW-Scoring integrates 11 algorithms to annotate and prioritize noncoding genetic variations, outperforming individual methods and identifying recurrently mutated regions in follicular lymphoma.