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single-cell-foundation-model-geneformer

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Use this skill when a task involves Geneformer workflows, especially TranscriptomeTokenizer input preparation, tokenized `.dataset` generation, cell or gene classification with `Classifier`, embedding extraction with `EmbExtractor`, and in silico perturbation analysis with `InSilicoPerturber`.

QUICK START

How to use this skill

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Source SKILL.md: https://github.com/PharMolix/OpenBioMed/blob/HEAD/skills/single-cell-foundation-model-scrna-seq-geneformer/SKILL.md

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Geneformer

Use This Skill When

Use this skill when the task involves official Geneformer workflows such as:

  • converting raw scRNA-seq data into Geneformer tokenized datasets
  • fine-tuning Geneformer for cell or gene classification
  • extracting cell or gene embeddings
  • generating state embeddings for downstream perturbation analysis
  • running in silico perturbation or in silico treatment style analyses
  • distinguishing pretrained zero-shot usage from fine-tuned classifier usage

This skill is for Geneformer-specific workflows, not generic single-cell model use.

Start Here

  1. Confirm the input is raw-count scRNA-seq data and still suitable for tokenization.
  2. Check that ensembl_id and n_counts are available.
  3. Tokenize first unless the user already has a Geneformer .dataset.
  4. Decide whether the task is classification, embedding extraction, or in silico perturbation.

Choose A Path

Tokenization

Use TranscriptomeTokenizer first for almost every Geneformer workflow. This step converts raw-count .loom or .h5ad data into tokenized datasets used by the downstream APIs.

Geneformer expects:

  • row attribute ensembl_id
  • cell attribute n_counts

Optional metadata can be passed through during tokenization.

Classification

Use Classifier for:

  • cell state classification
  • cell type annotation
  • gene classification tasks

The input is a tokenized Geneformer .dataset object, not raw AnnData.

Embedding extraction

Use EmbExtractor when the task is to:

  • extract CLS, cell, or gene embeddings
  • plot or inspect cell embeddings
  • generate state embeddings for later perturbation analysis

In silico perturbation

Use InSilicoPerturber for zero-shot or model-based perturbation analyses such as:

  • deleting or shifting genes
  • modeling start and goal cell states
  • ranking perturbations by movement toward a desired cell state

This is one of Geneformer's defining workflows and should be treated as more than ordinary classifier inference.

Guardrails

  • Do not pass feature-selected matrices into the tokenizer; the docs expect raw counts without feature selection.
  • Do not use gene symbols where the tokenizer expects ensembl_id.
  • Do not confuse tokenized .dataset files with AnnData objects.
  • Do not skip tokenization and jump directly to classifiers or perturbation APIs.
  • For perturbation tasks, be explicit about model type, embedding mode, and target cell states.

Official Workflow Surface

ComponentUse
TranscriptomeTokenizercreate tokenized datasets
Classifierfine-tune cell or gene classifiers
MTLClassifiermultitask cell classification
EmbExtractorextract and summarize embeddings
InSilicoPerturbersimulate perturbations / treatment directions

Read More Only If Needed

  • For operational usage and required input fields, read references/workflows.md.
  • For official source locations and model-specific notes, read references/sources-and-notes.md.