Summary
Carlos Najar is a computational biologist and Staff Scientist at the University of Chicago with a decade of experience developing scalable, reference-free methods for RNA-seq isoform analysis and multi-omics integration in neurological and immune disease cohorts. He earned a PhD from UC Berkeley, built widely adopted tools such as LeafCutter2, and led discovery that alternative splicing–mediated nonsense‑mediated decay (AS‑NMD) drives genetic effects on gene expression (Nature Genetics, 2024). His work spans single-cell and population-scale splicing, high-performance computing pipelines, and large consortia studies including GTEx and ADSP, where he uncovered disease-linked intron retention patterns. A mentor and interdisciplinary collaborator, he combines rigorous statistical method development with practical software engineering to translate splicing biology into reproducible analyses and community tools. An underappreciated thread in his profile is consistent focus on unannotated transcript structures, revealing biology missed by annotation‑centric approaches.
9 years of coding experience
2 years of employment as a software developer
Doctor of Philosophy - PhD, Computational Biology, Doctor of Philosophy - PhD, Computational Biology at University of California, Berkeley
Universidad Nacional Autónoma de México (UNAM)