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dynamo-preprocess

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Run or adapt dynamo preprocessing with `dynamo.preprocessing.Preprocessor`, including the `recipe` branches `monocle`, `seurat`, `sctransform`, `pearson_residuals`, and `monocle_pearson_residuals`. Use when converting or reproducing `docs/tutorials/notebooks/100_tutorial_preprocess.ipynb`, preprocessing an `AnnData` object for downstream dynamo analysis, customizing preprocessing kwargs, or translating notebook-level preprocessing into a reusable agent workflow.

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Dynamo Preprocess

Goal

Preprocess an AnnData object with the current dynamo.preprocessing.Preprocessor API, choose the correct recipe branch for the downstream task, customize kwargs before execution when needed, and validate that the expected keys and embeddings exist for later dynamo analysis.

Quick Workflow

  1. Inspect the user's data, environment, and downstream goal.
  2. Choose the recipe branch that matches the goal instead of defaulting blindly to the notebook's first example.
  3. Use Preprocessor.preprocess_adata(...) for the common case.
  4. If the user needs customization, call config_*_recipe(...), mutate kwargs, then run the matching recipe-specific method.
  5. If the user needs debugging or a custom pipeline, run the preprocessing steps individually in notebook order.
  6. Validate obs, var, layers, and obsm keys before treating preprocessing as complete.

Interface Summary

  • Preprocessor.preprocess_adata(adata, recipe='monocle', tkey=None, experiment_type=None) is the main wrapper.
  • The live source dispatches recipe across five branches: monocle, seurat, sctransform, pearson_residuals, monocle_pearson_residuals.
  • config_monocle_recipe(adata, n_top_genes=2000) is the only recipe config in this notebook family that exposes an extra tuning argument directly in the signature.
  • The constructor exposes many overridable callables and kwargs dictionaries, but the notebook mainly mutates: filter_cells_by_outliers_kwargs, filter_genes_by_outliers_kwargs, and select_genes_kwargs.

Read references/source-grounding.md before documenting parameters in more detail or when you need the exact inspected signatures.

Recipe Selection

  • Use monocle as the default when the goal is standard dynamo preprocessing for velocity or vector-field analysis.
  • Use seurat when the user specifically wants Seurat-style highly variable gene selection inside the current Preprocessor wrapper.
  • Use sctransform only when the user explicitly wants that transformation and the environment has KDEpy.
  • Use pearson_residuals when the goal is HVG selection and PCA on adata.X, not layer-preserving velocity normalization.
  • Use monocle_pearson_residuals when the user wants Pearson-residual-based feature selection and PCA but still needs monocle-style normalized layers for downstream velocity analysis.

Read references/recipe-selection.md before choosing a non-default recipe.

Minimal Execution Patterns

For the common case, use the wrapper:

import dynamo as dyn
from dynamo.preprocessing import Preprocessor

adata = dyn.sample_data.zebrafish()
preprocessor = Preprocessor()
preprocessor.preprocess_adata(adata, recipe="monocle")
dyn.tl.reduceDimension(adata, basis="pca")

For recipe customization, configure first, then mutate kwargs, then run the matching method:

import numpy as np
from dynamo.preprocessing import Preprocessor

preprocessor = Preprocessor()
preprocessor.config_monocle_recipe(adata)

preprocessor.filter_cells_by_outliers_kwargs = {
    "filter_bool": None,
    "layer": "all",
    "min_expr_genes_s": 300,
    "min_expr_genes_u": 100,
    "min_expr_genes_p": 50,
    "max_expr_genes_s": np.inf,
    "max_expr_genes_u": np.inf,
    "max_expr_genes_p": np.inf,
    "shared_count": None,
}

preprocessor.select_genes_kwargs = {
    "n_top_genes": 2500,
    "sort_by": "cv_dispersion",
    "keep_filtered": True,
    "SVRs_kwargs": {
        "relative_expr": True,
        "total_szfactor": "total_Size_Factor",
        "min_expr_cells": 0,
        "min_expr_avg": 0,
        "max_expr_avg": np.inf,
        "winsorize": False,
        "winsor_perc": (1, 99.5),
        "sort_inverse": False,
        "svr_gamma": None,
    },
}

preprocessor.preprocess_adata_monocle(adata)

For direct stepwise execution, follow the notebook spine:

  1. pp.standardize_adata(adata, tkey, experiment_type)
  2. pp.filter_cells_by_outliers(...)
  3. pp.filter_genes_by_outliers(...)
  4. pp.normalize_by_cells(...)
  5. pp.select_genes(...)
  6. pp.norm_method(...)
  7. pp.pca(...)
  8. dyn.tl.reduceDimension(adata, basis="pca")

Use the stepwise path for debugging or nonstandard workflows, not as the default wrapper replacement.

Validation

After preprocessing, check these items:

  • adata.obs may contain QC keys such as pass_basic_filter, Size_Factor, nGenes, nCounts, and pMito.
  • adata.var may contain pass_basic_filter, use_for_pca, and recipe-specific variability metrics.
  • adata.obsm["X_pca"] should exist after PCA-based recipes.
  • Layer-preserving workflows may create normalized layers such as X_spliced and X_unspliced.
  • dyn.tl.reduceDimension(adata, basis="pca") should run without shape or key errors.

If notebook-style visualization parity matters, the standard post-check is:

dyn.tl.reduceDimension(adata, basis="pca")
dyn.pl.umap(adata, color=celltype_key)

Constraints

  • Do not assume the notebook covers every recipe branch; the live source adds monocle_pearson_residuals as a distinct hybrid path.
  • Pearson residuals and sctransform are intended for adata.X; using them on velocity-relevant layers can create downstream problems.
  • sctransform requires KDEpy.
  • dyn.sample_data.zebrafish() may require data download if the dataset is not cached.
  • Prefer the current dynamo.preprocessing.Preprocessor API over older recipe helpers unless the user explicitly asks for legacy behavior.

Resource Map

  • Read references/recipe-selection.md for branch-by-branch guidance.
  • Read references/source-notebook-map.md to trace each part of the notebook to the generated skill.
  • Read references/source-grounding.md for inspected signatures, doc-derived notes, and source-level recipe branch evidence.
  • Read references/compatibility.md when notebook prose and current source behavior may have drifted.