pylimma documentation ===================== pylimma is a faithful Python port of R limma, the most widely used Bioconductor package for differential expression analysis. It provides the full linear-modelling pipeline (``lm_fit``, ``contrasts_fit``, ``e_bayes``, ``top_table``), voom for RNA-seq, gene-set testing (camera, roast, fry, romer), normalisation, batch correction, and differential splicing - all validated to match R limma output within ``rtol=1e-6`` on fixture parity tests. pylimma accepts numpy arrays, pandas DataFrames, AnnData objects, or limma-style ``EList`` dict subclasses, with centralised polymorphic dispatch so the same code works across the scverse ecosystem and R-style workflows. Quickstart ---------- .. code-block:: python import numpy as np from pylimma import lm_fit, contrasts_fit, e_bayes, top_table expr = np.random.normal(size=(100, 6)) design = np.column_stack([np.ones(6), [0, 0, 0, 1, 1, 1]]) fit = lm_fit(expr, design) fit = contrasts_fit(fit, contrasts=np.array([[0], [1]])) fit = e_bayes(fit) print(top_table(fit, coef=0).head()) See :doc:`quickstart` for the full walk-through. Contents -------- .. toctree:: :maxdepth: 2 installation quickstart api .. toctree:: :maxdepth: 2 :caption: Worked examples tutorials/all_chiaretti tutorials/gse60450 tutorials/pasilla tutorials/yoruba tutorials/kang_pbmc tutorials/mulvey .. toctree:: :maxdepth: 2 :caption: Validation validation/parity_report validation/known_differences validation/fixtures validation/benchmarks Citation -------- Please cite the original limma papers when using pylimma: - Smyth, G. K. (2004). Linear models and empirical Bayes methods for assessing differential expression in microarray experiments. *Statistical Applications in Genetics and Molecular Biology* 3, Article 3. - Ritchie, M. E., Phipson, B., Wu, D., Hu, Y., Law, C. W., Shi, W., and Smyth, G. K. (2015). limma powers differential expression analyses for RNA-sequencing and microarray studies. *Nucleic Acids Research* 43(7), e47. - Law, C. W., Chen, Y., Shi, W., and Smyth, G. K. (2014). voom: precision weights unlock linear model analysis tools for RNA-seq read counts. *Genome Biology* 15, R29. A pylimma preprint / Zenodo DOI will be listed here once published. Until then, cite the GitHub repository and the version tag. Indices ------- * :ref:`genindex` * :ref:`modindex` * :ref:`search`