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zongtingwei

Community

@zongtingwei · Shenzhen

29Followers
|
11Public Repos
|
66Published Skills

Studying Agent and AIVC.

Agent Skills by zongtingwei

Showing 66 vetted skills indexed across 1 GitHub repositories.

zongtingweizongtingwei
25

ehr-analysis

Automate end-to-end EHR predictive modeling workflows with PyHealth.

Community
Advanced
zongtingweizongtingwei
25

long-read-genomics

Process nanopore or PacBio long-read data into alignments, polished consensus, and variant summaries.

Community
Intermediate
zongtingweizongtingwei
25

copy-number

Automate copy-number estimation, segmentation, annotation, and visualization from coverage data.

Community
Intermediate
zongtingweizongtingwei
25

genome-assembly

Generate de novo genome assemblies from short and long reads with QC and contamination assessment.

Community
Intermediate
zongtingweizongtingwei
25

variant-calling

Identify germline, somatic, and structural variants from BAM/CRAM sequencing data.

Community
Advanced
zongtingweizongtingwei
25

comparative-genomics

Generates orthologs, synteny blocks, and evolutionary summaries from genome assemblies and annotations.

Community
Advanced
zongtingweizongtingwei
25

phasing-imputation

Generates phased and imputed genotypes from VCF data using reference panels and Python tools.

Community
Advanced
zongtingweizongtingwei
25

systems-biology

Automate flux balance analysis and metabolic modeling with cobrapy for Python-based workflows.

Community
Advanced
zongtingweizongtingwei
25

multi-omics-integration

Integrate matched omics layers into shared latent factors for cross-modal analysis.

Community
Advanced
zongtingweizongtingwei
25

machine-learning-for-omics

Train supervised models on omics feature matrices and output metrics and explanations.

Community
Advanced
zongtingweizongtingwei
25

causal-genomics

Integrate GWAS and QTL summary statistics to identify shared causal signals.

Community
Advanced
zongtingweizongtingwei
25

pathway-analysis

Automate pathway enrichment and interpretation across multi-omics gene lists.

Community
Advanced
zongtingweizongtingwei
25

cell-communication

Infer ligand-receptor signaling from scRNA-seq or spatial data using pandas.

Community
Intermediate
zongtingweizongtingwei
25

spatial-transcriptomics

Preprocess spatial transcriptomics data to identify domains and deconvolute cell types.

Community
Intermediate
zongtingweizongtingwei
25

scrna-preprocessing-clustering

Preprocess single-cell RNA-seq data into analysis-ready AnnData objects.

Community
Advanced
zongtingweizongtingwei
25

cell-annotation

Annotate single-cell RNA-seq data with cell-type labels using marker review and reference transfer.

Community
Intermediate
zongtingweizongtingwei
25

trajectory-lineage

Infer pseudotime, lineage branches, and state transitions from single-cell data using Scanpy.

Community
Intermediate
zongtingweizongtingwei
25

multiome-scatac

Integrate single-cell RNA and ATAC data into unified multimodal embeddings.

Community
Advanced
zongtingweizongtingwei
25

alternative-splicing

Identify and quantify splice events and isoform usage from RNA-seq data.

Community
Advanced
zongtingweizongtingwei
25

rna-quantification

Quantify gene and transcript abundances from RNA-seq reads using salmon, kallisto, or featureCounts.

Community
Advanced
zongtingweizongtingwei
25

differential-expression

Perform count-based differential expression analysis on bulk RNA-seq data with PyDESeq2.

Community
Advanced
zongtingweizongtingwei
25

bulk-rna-expression

Normalize and quality-check bulk RNA-seq count matrices with Python.

Community
Advanced
zongtingweizongtingwei
25

ribo-seq

Automate ribosome profiling analysis from raw reads to translation efficiency insights.

Community
Advanced
zongtingweizongtingwei
25

small-rna-seq

Process small RNA FASTQ files into counts, differential results, and target summaries.

Community
Intermediate