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GPTomics AI Skills

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Browse published AI skills maintained by GPTomics. Compare skill descriptions and follow each source repository for setup instructions.

Author statistics

Indexed skills

269

Repository stars across indexed skills

80,661

Repository forks

13,719

Average repository stars per indexed skill

300

Repository stars may repeat across skills from the same repository.

269 skills

Browse skills

GitHub

bio-workflows-imc-pipeline

GPTomics

End-to-end imaging mass cytometry workflow from raw acquisitions to spatial cell analysis. Orchestrates image preprocessing, segmentation, phenotyping, and spatial statistics.

GitHub

bio-workflows-scrnaseq-pipeline

GPTomics

End-to-end single-cell RNA-seq workflow from 10X Genomics data to annotated cell types. Covers QC, normalization, clustering, marker detection, and cell type annotation.

GitHub

bio-read-qc-umi-processing

GPTomics

Extract, process, and deduplicate reads using Unique Molecular Identifiers (UMIs) with umi_tools. Use when library prep includes UMIs and accurate molecule counting is needed, such as in single-cell RNA-seq, lo...

GitHub

bio-pathway-enrichment-visualization

GPTomics

Visualize enrichment results using enrichplot package functions. Covers dotplot, barplot, cnetplot, emapplot, gseaplot2, ridgeplot, and treeplot for clusterProfiler results.

GitHub

bio-phylo-tree-io

GPTomics

Read, write, and convert phylogenetic tree files using Biopython Bio.Phylo. Use for parsing Newick, Nexus, PhyloXML, and NeXML tree formats, converting between formats, and handling multiple trees in a single f...

GitHub

bio-workflows-longread-sv-pipeline

GPTomics

End-to-end workflow for detecting structural variants from long-read sequencing data. Covers ONT/PacBio alignment with minimap2 and SV calling with Sniffles or cuteSV.

GitHub

bio-phasing-imputation-haplotype-phasing

GPTomics

Phase genotypes into haplotypes using Beagle or SHAPEIT. Resolves which alleles are inherited together on each chromosome. Use when preparing VCF files for imputation, HLA typing, or population genetic analyses...

GitHub

bio-bedgraph-handling

GPTomics

Create, manipulate, and convert bedGraph files for genome browser visualization. Covers bedGraph format, conversion to/from bigWig, normalization, and signal processing. Use for handling coverage and signal tra...

GitHub

bio-batch-processing

GPTomics

Process multiple sequence files in batch using Biopython. Use when working with many files, merging/splitting sequences, or automating file operations across directories.

GitHub

bio-metagenomics-visualization

GPTomics

Visualize metagenomic profiles using R (phyloseq, microbiome) and Python (matplotlib, seaborn). Create stacked bar plots, heatmaps, PCA plots, and diversity analyses. Use when creating publication-quality figur...

GitHub

bio-paired-end-fastq

GPTomics

Handle paired-end FASTQ files (R1/R2) using Biopython. Use when working with Illumina paired reads, synchronizing pairs, interleaving/deinterleaving, or filtering paired data.

GitHub

bio-workflows-spatial-pipeline

GPTomics

End-to-end spatial transcriptomics workflow for Visium/Xenium data. Covers data loading, preprocessing, spatial analysis, domain detection, and visualization with Squidpy.

GitHub

bio-genome-intervals-bigwig-tracks

GPTomics

Create and read bigWig browser tracks for visualizing continuous genomic data. Convert bedGraph to bigWig, extract signal values, and generate coverage tracks using UCSC tools and pyBigWig. Use when preparing c...

GitHub

bio-vcf-manipulation

GPTomics

Merge, concatenate, sort, intersect, and subset VCF files using bcftools. Use when combining variant files, comparing call sets, or restructuring VCF data.

GitHub

bio-crispr-library-design

GPTomics

CRISPR library design for genetic screens. Covers sgRNA selection, library composition, control design, and oligo ordering. Use when designing custom sgRNA libraries for knockout, activation, or interference sc...

GitHub

bio-workflows-multiome-pipeline

GPTomics

End-to-end multiome workflow for joint scRNA-seq + scATAC-seq analysis. Covers data loading, separate modality processing, and WNN integration with Seurat/Signac.

GitHub

bio-proteomics-quantification

GPTomics

Protein quantification from mass spectrometry data including label-free (LFQ, intensity-based), isobaric labeling (TMT, iTRAQ), and metabolic labeling (SILAC) approaches. Use when extracting protein abundances...

GitHub

bio-flow-cytometry-bead-normalization

GPTomics

Bead-based normalization for CyTOF and high-parameter flow cytometry. Covers EQ bead normalization, signal drift correction, and batch normalization. Use when correcting instrument drift in CyTOF or harmonizing...

GitHub

bio-genome-assembly-assembly-qc

GPTomics

Assess genome assembly quality using QUAST for contiguity metrics and BUSCO for completeness. Essential for evaluating assembly success and comparing assemblers.

The default order uses GitHub repository stars from our indexed data. Stars belong to the source repository and may be shared by multiple skills. They indicate repository interest, not skill installs or an independent quality score.