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Agent Skills in category: bioinformatics

143 skills match this category. Browse curated collections and explore related Agent Skills.

bioservices

Primary Python tool for 40+ bioinformatics services. Preferred for multi-database workflows: UniProt, KEGG, ChEMBL, PubChem, Reactome, QuickGO. Unified API for queries, ID mapping, pathway analysis. For direct REST control, use individual database skills (uniprot-database, kegg-database).

pythonmulti-databaseuniprotkegg
ovachiever
ovachiever
81

chembl-database

Query ChEMBL's bioactive molecules and drug discovery data. Search compounds by structure/properties, retrieve bioactivity data (IC50, Ki), find inhibitors, perform SAR studies, for medicinal chemistry.

cheminformaticsdrug-discoverybioactivity-datamedicinal-chemistry
ovachiever
ovachiever
81

cellxgene-census

Query CZ CELLxGENE Census (61M+ cells). Filter by cell type/tissue/disease, retrieve expression data, integrate with scanpy/PyTorch, for population-scale single-cell analysis.

single-cell-rna-seqscanpypytorchpopulation-scale-analysis
ovachiever
ovachiever
81

clinpgx-database

Access ClinPGx pharmacogenomics data (successor to PharmGKB). Query gene-drug interactions, CPIC guidelines, allele functions, for precision medicine and genotype-guided dosing decisions.

pharmacogenomicsgene-drug-interactionsprecision-medicineclinical-decision-support
ovachiever
ovachiever
81

dendrite-reforging-protocol

Reforge neural dendrite patterns after catastrophic failure.

neural-networksdendritesbrain-repairpattern-recognition
starwreckntx
starwreckntx
1

go-db-query

Skills for querying Gene Ontology annotation databases in DuckDB format. Use this for queries about GO annotations, genes, terms, evidence codes, or taxonomic relationships in GO-DB databases (db/*.ddb files). Particularly useful for hierarchical queries using closure tables to find genes annotated to terms and their descendants.

gene-ontologydatabase-querieshierarchical-queriesDuckDB
cmungall
cmungall
1

ChIPseq-QC

Performs ChIP-specific biological validation. It calculates metrics unique to protein-binding assays, such as Cross-correlation (NSC/RSC) and FRiP. Use this when you have filtered the BAM file and called peaks for ChIP-seq data. Do NOT use this skill for ATAC-seq data or general alignment statistics.

chip-seqbiological-validationprotein-binding-assayscross-correlation
BIsnake2001
BIsnake2001
32

correlation-methylation-epiFeatures

This skill provides a complete pipeline for integrating CpG methylation data with chromatin features such as ATAC-seq signal, H3K27ac, H3K4me3, or other histone marks/TF signals.

methylationchromatin-accessibilityepiFeaturesATAC-seq
BIsnake2001
BIsnake2001
32

hic-compartment-shift

This skill performs A/B compartment shift analysis between two Hi-C samples.

hiccompartment-shiftchromatin-structuregenomics
BIsnake2001
BIsnake2001
32

regulatory-community-analysis-ChIA-PET

This skill performs protein-mediated regulatory community analysis from ChIA-PET datasets and provide a way for visualizing the communities. Use this skill when you have a annotated peak file (in BED format) from ChIA-PET experiment and you want to identify the protein-mediated regulatory community according to the BED and BEDPE file from ChIA-PET.

ChIA-PETprotein-mediated-regulationregulatory-community-analysisgenomic-intervals
BIsnake2001
BIsnake2001
32

atac-footprinting

This skill performs transcription factor (TF) footprint analysis using TOBIAS on ATAC-seq data. It corrects Tn5 sequence bias, quantifies TF occupancy at motif sites, generates footprint scores, and optionally compares differential TF binding across conditions.

atac-seqtranscription-factor-footprintingtobiastf-occupancy
BIsnake2001
BIsnake2001
32

methylation-variability-analysis

This skill provides a complete and streamlined workflow for performing methylation variability and epigenetic heterogeneity analysis from whole-genome bisulfite sequencing (WGBS) data. It is designed for researchers who want to quantify CpG-level variability across biological samples or conditions, identify highly variable CpGs (HVCs), and explore epigenetic heterogeneity.

methylation-analysisepigeneticswhole-genome-bisulfite-sequencingCpG-variability
BIsnake2001
BIsnake2001
32

differential-region-analysis

The differential-region-analysis pipeline identifies genomic regions exhibiting significant differences in signal intensity between experimental conditions using a count-based framework and DESeq2. It supports detection of both differentially accessible regions (DARs) from open-chromatin assays (e.g., ATAC-seq, DNase-seq) and differential transcription factor (TF) binding regions from TF-centric assays (e.g., ChIP-seq, CUT&RUN, CUT&Tag). The pipeline can start from aligned BAM files or a precomputed count matrix and is suitable whenever genomic signal can be summarized as read counts per region.

deseq2genomic-intervalschip-seqatac-seq
BIsnake2001
BIsnake2001
32

chromatin-state-inference

This skill should be used when users need to infer chromatin states from histone modification ChIP-seq data using chromHMM. It provides workflows for chromatin state segmentation, model training, state annotation.

chromHMMchip-seqchromatin-state-inferencehistone-modifications
BIsnake2001
BIsnake2001
32

genomic-feature-annotation

This skill is used to perform genomic feature annotation and visualization for any file containing genomic region information using Homer (Hypergeometric Optimization of Motif EnRichment). It annotates regions such as promoters, exons, introns, intergenic regions, and TSS proximity, and generates visual summaries of feature distributions.

genomic-intervalshomergenomic-annotationvisualization
BIsnake2001
BIsnake2001
32

loop-annotation

This skill annotates chromatin loops, including enhancer/promoter assignments, CTCF-peak overlap. It automatically constructs enhancer and promoter sets when missing and outputs standardized loop categories.

chromatin-loopsenhancer-promoter-assignmentCTCF-peak-overlapgenomic-annotation
BIsnake2001
BIsnake2001
32

hic-normalization

Automatically detect and normalize Hi-C data. Only .cool or .mcool file is supported. All .mcool files are then checked for existing normalization (supports bins/weight only) and balanced if none of the normalizations exist.

hicnormalizationcool-formatmcool-format
BIsnake2001
BIsnake2001
32

hic-loop-calling

This skill performs chromatin loop detection from Hi-C .mcool files using cooltools.

chromatin-loopinghic-datacooltoolsmcool
BIsnake2001
BIsnake2001
32

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