HansenHeLab
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cfMeDIP-seq_Data_Resource_Codes
cfMeDIP-seq_Data_Resource_Codes PublicCode and workflows for the cfMeDIP‑seq Data Resource: end‑to‑end methylation & fragmentomic feature extraction, PCA, and machine‑learning classifiers (cancer vs normal, cancer type & subtype) from …
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Epitranscriptomic_m6A_Profiling_in_LUAD_Data_and_Codes
Epitranscriptomic_m6A_Profiling_in_LUAD_Data_and_Codes Public -
uniqueCount
uniqueCount PublicThis tool counts reads in unique regions on genes and calculated RPKM based on the adjusted gene length
Repositories
- FunCircDB Public
- cfMeDIP-seq_Data_Resource_Codes Public
Code and workflows for the cfMeDIP‑seq Data Resource: end‑to‑end methylation & fragmentomic feature extraction, PCA, and machine‑learning classifiers (cancer vs normal, cancer type & subtype) from Zeng and Abelman et al. (2025)
- m6a-crispr-casRx-publish Public
Epitranscriptomic Editing Screening Identifies Functional m6A Sites in Cancer
- memo-eQTL_Data_Codes Public
- HansenHeLab.github.io Public
- RARE Public
Risk Associated Regulatory Region/Enhancer (RARE) is a computational method to prioritize open chromatin regions in order of their potential to cause risk.
- uniqueCount Public
This tool counts reads in unique regions on genes and calculated RPKM based on the adjusted gene length
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