Samantha Zarate is a computational genomics leader with ~10 years of experience bridging research and production-scale sequencing informatics, currently leading Sequencing Informatics Research at Regeneron. Trained at Stanford and Johns Hopkins (PhD candidate in Mike Schatz’s lab), she has deep expertise in variant calling, large-scale realignment, and migrating datasets to new references—work that contributed to a co-first authored Science analysis of the T2T-CHM13 reference. Her background includes productizing bioinformatics tools at DNAnexus, developing features for DeepVariant at Google Health, and scaling analyses for hundreds of thousands of exomes at Regeneron. She combines hands-on algorithm and pipeline development with teaching and documentation experience, and has a track record of making complex genomics methods reproducible and cloud-ready. An under-the-radar strength is her ability to translate bleeding-edge reference and variant-calling advances into practical, enterprise-ready workflows used by large genomic centers.
10 years of coding experience
5 years of employment as a software developer
Johns Hopkins University
Bachelor's Degree, Biomedical Computation, Bachelor's Degree, Biomedical Computation at Stanford University
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