Experience in WGS, WTS/RNA-seq, DNA methylation, long-read sequencing, ATAC-seq, HiChIP/chromatin-contact data, scRNA-seq, scATAC-seq, cancer genomics, structural variation, R, Linux/HPC, version control, and reproducible workflows. Coordinates long-read sequencing and DNA methylation analysis to identify cryptic regulatory and structural variants in pediatric leukemia/lymphoma, that includes breakpoint interpretation, allelic phasing, methylation-aware analysis, and integration with transcriptomic evidence.