Pinned Repositories
3DCoop
Inferring cell type-specific transcriptional regulators cooperation in the context of 3D chromatin
CAUSALdb-finemapping-pip
A GWAS fine-mapping pipeline used in CAUSALdb
cepip
Context-dependent epigenomic weighting for regulatory variant prioritization
CHANCE
Personalized non-oncology drug repurposing for cancer treatment
epiCOLOC
Integrating large-scale and context-dependent epigenomics features for comprehensive colocalization analysis
LoopAnchor
Quantitative modeling of CTCF-mediated loop anchors
mulinlab-pip
mulinlab bioinformatics pipelines for reproducible, efficient and convenient bioinformatics research.
regBase
Base-wise aggregation and functional prediction for human non-coding regulatory variants
VarNote
Fast and scalable variant annotation tool
vSampler
Fast and annotation-based matched variant sampling tool
mulinlab's Repositories
mulinlab/VarNote
Fast and scalable variant annotation tool
mulinlab/CAUSALdb-finemapping-pip
A GWAS fine-mapping pipeline used in CAUSALdb
mulinlab/regBase
Base-wise aggregation and functional prediction for human non-coding regulatory variants
mulinlab/mulinlab-pip
mulinlab bioinformatics pipelines for reproducible, efficient and convenient bioinformatics research.
mulinlab/epiCOLOC
Integrating large-scale and context-dependent epigenomics features for comprehensive colocalization analysis
mulinlab/LoopAnchor
Quantitative modeling of CTCF-mediated loop anchors
mulinlab/3DCoop
Inferring cell type-specific transcriptional regulators cooperation in the context of 3D chromatin
mulinlab/cepip
Context-dependent epigenomic weighting for regulatory variant prioritization
mulinlab/CHANCE
Personalized non-oncology drug repurposing for cancer treatment
mulinlab/vSampler
Fast and annotation-based matched variant sampling tool
mulinlab/FIND
Stratifying variant pathogenicity and trait-modulating effect under human recent adaption