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Hi there 👋

  • 🔮 I'm dabbling into the data analysis of single-cell RNA sequencing, DNA methylation and variant calling
  • 🎉 I'm super excited about using single-cell multi-omics to address biomedical questions
  • 💾 I'm using R (intensively), Python/Snakemake (frequently) and Shell (frequently). Had experience with C and MATLAB but cannot remember much. Always ready to learn new skills if necessary

Zhiyuan Hu's Projects

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Code for Liu, Y., Hu, Z., Cheng, J. et al. Subtraction-free and bisulfite-free specific sequencing of 5-methylcytosine and its oxidized derivatives at base resolution. Nat Commun 12, 618 (2021). https://doi.org/10.1038/s41467-021-20920-2

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R package CIDER: Meta-Clustering for Single-Cell Data Integration and Evaluation

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R package to predict mutations whether can elicit nonsense-mediated decay or not

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A pan-cancer genome-wide analysis reveals tumour dependencies by induction of nonsense-mediated decay

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Z Hu et al. The repertoire of serous ovarian cancer non-genetic heterogeneity revealed by single-cell sequencing of normal fallopian tube epithelial cells. Cancer Cell (2020). Volume 37, Issue 2, P226-242

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Styles for The Carpentries lessons. Documentation at http://carpentries.github.io/lesson-example/.

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