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Yakir Reshef

I am an MD/PhD computer scientist currently training in internal medicine at Brigham and Women's Hospital. I joined the Raychaudhuri lab in 2019 and have been working on developing new methods for comparing single-cell data from multiple conditions. In 2018, I completed a PhD in computer science at...

Ryan Agnew

I recently graduated from Saint Michael’s College where I majored in Biology and minored in Chemistry. During my time as an undergrad, I studied gene regulation in maize and CCAP expression in the tiger wandering spider. I am now interested in learning more about human genetics and studying the...

Siddarth Gurajala

I grew up around Seattle, Washington for most of my life, and graduated from the University of Washington in 2021 with a Bachelor of Science in Biochemistry. My undergraduate work was focused on characterizing the epigenomic landscape of a human embryonic stem cell pluripotency transition, as well...

Amber Shen

Amber is a senior at MIT studying math from Boulder, Colorado. She is interested in methods development and understanding gene regulatory networks. Outside of doing research, Amber enjoys playing tennis, hiking, and exploring new coffee places.

Cristian Valencia

I'm a postdoctoral fellow that is interested in applying genetics and genomics to understand the interindividual variability on immune-related phenotypes. I joined the Raychaudhuri lab in 2021 and I am working on integrating single cell multi-omic thechnologies to better understand the genetics and...

Dylan Kotliar

I’m a Medical Resident at Harvard Medical School in the Health Sciences and Technology track. I did my Ph.D in Pardis Sabeti’s lab at the Broad Institute in the Harvard Systems Biology PhD program. My Ph.D combined computational and experimental biology with field work in Nigeria, Liberia, and...

Mujin Kwun

Samira Asgari joins the lab

Samira Asgari recently completed her doctoral studies at Ecole Polytechnique Fédérale de Lausanne. Asgari is funded by a fellowship from the Swiss National Science Foundation to explore rare variants in exome sequencing data in our tuberculosis cohort.