biotapy

biotapy is a microbiome analysis toolkit for Python, in the style of R's mia and phyloseq, built on AnnData/TreeData. Samples are always rows, the count matrix stays sparse, the phylogenetic tree sits alongside the data as a first-class object, and every computation with an R equivalent is checked against R on real data.

Status

biotapy 0.2 is an early release. The API can still change between minor versions.

What 0.2 does (full signatures in the API reference):

• Readers: bt.io.read_biom (BIOM 1.0/2.1), bt.io.read_qiime2 (.qza artifacts, no QIIME 2 install needed), bt.io.read_dada2 (CSV/TSV/.rds sequence tables), bt.io.read_phyloseq (.rds/.RData, no R needed) and bt.io.read_metaphlan (MetaPhlAn 3 and 4 profiles) all read into one TreeData. bt.io.read_humann and bt.io.read_picrust2 read function tables into a MuData with a community and a per-taxon modality; bt.io.read_picrust2_traits reads PICRUSt2's per-ASV gene copy numbers.
• Writer: bt.io.write_biom writes a BIOM 2.1 or 1.0 table back out.
• Datasets: bt.datasets.toy and bt.datasets.toy_humann (in-memory, for examples and tests), bt.datasets.global_patterns, bt.datasets.enterotype and bt.datasets.esophagus (phyloseq's example datasets), bt.datasets.hmp2 (the HMP2 inflammatory bowel disease cohort) and bt.datasets.enzyme (the ENZYME EC hierarchy), downloaded and cached on first use.
• Preprocessing: bt.pp.relative, bt.pp.tax_glom, bt.pp.filter_features, bt.pp.filter_samples and bt.pp.rarefy.
• Function: bt.fn.load_hierarchy, bt.fn.func_glom and bt.fn.renorm (checked against HUMAnN's own output), bt.fn.contributions and bt.fn.functional_redundancy.
• Tools: bt.tl.alpha, bt.tl.beta, bt.tl.unifrac, bt.tl.pcoa, bt.tl.nmds and bt.tl.permanova, each checked against R on real data.
• Plots: bt.pl.bar, bt.pl.richness, bt.pl.ordination, bt.pl.scree, bt.pl.heatmap and bt.pl.contributions.

Next, in 0.3: compositional transforms (CLR, PhILR) and differential abundance (ANCOM-BC, LinDA, ALDEx2, MaAsLin 3) behind one result format. See the roadmap; no dates are promised.

Installation

You need Python 3.12 or newer.

pip install biotapy

or, with uv:

uv add biotapy

or, with pixi, in a workspace that has Python 3.12 or newer:

pixi add "python>=3.12"
pixi add --pypi biotapy

The development version installs straight from GitHub: pip install git+https://github.com/pedrocr83/biotapy.git.

On Python 3.14, the biom-format dependency has no wheels yet, so it is built from source and needs a C compiler until biom-format publishes 3.14 wheels (biocore/biom-format#1004).

Quick start

Load the bundled toy dataset, add relative abundance, and aggregate to phylum:

import biotapy as bt

tdata = bt.datasets.toy()
tdata.shape  # (6, 8): 6 samples, 8 features

rel = bt.pp.relative(tdata)
rel.layers["relative"][0].sum()  # 1.0, X itself is untouched

glom = bt.pp.tax_glom(tdata, "phylum")
glom.n_vars  # 3: features sharing a lineage down to phylum are merged

Reading your own data

Each reader returns a TreeData following the same data model. Only the first argument is required; the keyword arguments attach taxonomy, sample metadata and a phylogenetic tree where the format supports them.

# BIOM 1.0 (JSON) or 2.1 (HDF5), dialect detected automatically
tdata = bt.io.read_biom("table.biom", tree="tree.nwk")

# QIIME 2 artifacts (.qza), no QIIME 2 install required
tdata = bt.io.read_qiime2(
    "table.qza", taxonomy="taxonomy.qza", tree="tree.qza", metadata="sample-metadata.tsv"
)

# DADA2 sequence tables: CSV, TSV or R's .rds, with optional taxonomy and tree
tdata = bt.io.read_dada2("seqtab.rds", taxa="taxa.rds", tree="tree.nwk")

# phyloseq objects saved from R with saveRDS()/save() - no R, no rpy2
tdata = bt.io.read_phyloseq("ps.rds")
# an .RData file can hold several phyloseq objects; pick one by its R variable name
tdata = bt.io.read_phyloseq("ps.RData", name="ps_16S")

Write back out to BIOM with bt.io.write_biom(tdata, "table.biom").

Example datasets

bt.datasets.global_patterns(), bt.datasets.enterotype() and bt.datasets.esophagus() download phyloseq's example datasets once and cache them on disk with pooch; later calls reuse the cache with no network access, as long as the hash still matches. Set BIOTAPY_DATA_DIR to change the cache directory:

import biotapy as bt

gp = bt.datasets.global_patterns()  # 26 samples, 19,216 OTUs
gp.shape

Saving your work

A TreeData round-trips through treedata's own format, tree included:

tdata.write_h5td("tdata.h5td")

import treedata as td

back = td.read_h5td("tdata.h5td")

Dropping down to plain AnnData (no tree) works the usual way too: tdata.write_h5ad("tdata.h5ad") / anndata.read_h5ad("tdata.h5ad").

The data model

Every biotapy function reads and writes the same object, a TreeData (an AnnData that also carries a phylogeny):

See the data model guide for the full slot list (including the ones diversity and ordination write) and the data-model-slots contract for the exact rules.

Every function is pure by default: it returns a new object or its result and leaves the one you passed in unchanged. Only a tl function called with inplace=True writes its result into it (obs, obsp, obsm and uns["biotapy"]).

Coming from R

Every function's docstring names its R equivalent (phyloseq::tax_glom, mia::agglomerateByRank, and so on) in its Notes section, and the Coming from R page lists them all, with the phyloseq accessors that are plain AnnData code. The phyloseq analysis vignette is redone with biotapy in the tutorials.

Example data and licensing

bt.datasets.global_patterns, bt.datasets.enterotype and bt.datasets.esophagus download example data from phyloseq's repository at runtime; biotapy ships none of it. That data stays licensed to phyloseq's authors under AGPL-3. bt.datasets.enzyme downloads ENZYME, distributed by the SIB Swiss Institute of Bioinformatics under CC BY 4.0. bt.datasets.hmp2 downloads the HMP2 tables from the IBDMDB, which states no licence for them; cite Lloyd-Price et al. (2019, Nature 569:655-662) when you use them. biotapy itself is BSD-3-Clause.

Documentation

Full documentation, including the user guide and API reference, is at biotapy.readthedocs.io.

Development

uv sync --group dev --group test --group doc
uvx prek run --all-files
uv run --group test pytest

Network and golden tests (downloads data, compares against R) are excluded by default; run them explicitly with:

uv run --group test pytest -m "network or golden"

Regenerating the R golden files themselves needs the pinned R container - see the regenerate-golden-files playbook.

All contributions follow rules.md and the knowledge bundle (decisions, contracts, roadmap).

Release notes

See the changelog.

Contact

Questions, bug reports and feature requests all go to the issue tracker.

Citation

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