Author
Broad InstituteORCID 0000-0001-9548-4420Unclaimed ORCID profile · follow to get notified of new preprints
3 papers
Recent·Most cited
Samuel Maffa, Isabella Boyle, Lie Ward…·Joshua M. Dempster
The paper uses Perturb-seq to analyze gene knockouts in cancer cell lines, identifying context-specific gene dependencies and transcriptional responses.
Declan Bennett, Monika Wierdl, S Chakraborty…·Lillian M. Guenther
The paper develops ALTitude, a machine learning model to predict ALT status from whole genome sequencing data, identifies SMARCAL1 as a therapeutic target in ALT-driven cancers.
Qian Qin, Victoria Popic, Houlin Yu…·Brian J. Haas
CTAT-LR-fusion detects fusion transcripts from long and short read RNA-seq data, improving accuracy in bulk and single cell transcriptomes.