supremo_lite

User Guide

  • Personalized Genome Generation
  • Variant-Centered Sequence Windows
  • PAM Disruption Analysis
  • Prediction Alignment
  • Prediction Alignment Examples
  • Variant Type Examples
  • Saturation Mutagenesis

Notebooks

  • Getting Started with supremo_lite
  • Personalized Genome Generation
  • Prediction Alignment: From Sequences to Aligned Predictions
  • PAM Disruption Analysis: Identifying CRISPR-Resistant Variants
  • In-Silico Mutagenesis and Scrambled Controls

Reference

  • API Reference
    • supremo_lite
  • Changelog
  • Contributing
  • Code of Conduct
supremo_lite
  • API Reference
  • Edit on GitHub

API Reference

This page contains auto-generated API reference documentation [1].

  • supremo_lite
    • supremo_lite.chromosome_utils
    • supremo_lite.core
    • supremo_lite.mock_models
      • supremo_lite.mock_models.testmodel_1d
      • supremo_lite.mock_models.testmodel_2d
    • supremo_lite.mutagenesis
    • supremo_lite.personalize
    • supremo_lite.prediction_alignment
    • supremo_lite.sequence_utils
    • supremo_lite.variant_utils
[1]

Created with sphinx-autoapi

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