A de novo assembly-based fusion gene detection workflow using DNA sequencing data to identify fusion breakpoints
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Updated
Feb 20, 2026 - Makefile
A de novo assembly-based fusion gene detection workflow using DNA sequencing data to identify fusion breakpoints
exploring microsatellites in the human genome
R and Python workflows for Ewing sarcoma cancer genomics: 1q gain, survival, transcriptomics and driver prioritization. Includes an offline synthetic demo.
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