Train a machine learning model on a collection

Here, we iterate over the artifacts within a collection to train a machine learning model at scale.

import lamindb as ln

→ connected lamindb: testuser1/test-scrna

ln.context.uid = "Qr1kIHvK506r0000"
ln.context.track()

→ notebook imports: lamindb==0.76.4 torch==2.4.1

→ created Transform('Qr1kIHvK506r0000') & created Run('2024-09-06 08:29:05.133365+00:00')

Query our collection:

collection = ln.Collection.get(
    name="My versioned scRNA-seq collection", version="2"
)
collection.describe()

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Collection(uid='MJM8a4PbeVFk6j980001', version='2', is_latest=True, name='My versioned scRNA-seq collection', hash='dBJLoG6NFZ8WwlWqnfyFdQ', visibility=1, updated_at='2024-09-06 08:28:38 UTC')
  Provenance
    .created_by = 'testuser1'
    .transform = 'Standardize and append a batch of data'
    .run = '2024-09-06 08:28:17 UTC'
    .input_of_runs = ["'2024-09-06 08:28:48 UTC'"]
  Feature sets
    'var' = 'MIR1302-2HG', 'FAM138A', 'OR4F5', 'None', 'OR4F29', 'OR4F16', 'LINC01409', 'FAM87B', 'LINC01128', 'LINC00115', 'FAM41C'
    'obs' = 'donor', 'tissue', 'cell_type', 'assay'

Create a map-style dataset

Let us create a map-style dataset using using mapped(): a MappedCollection. This is what, for example, the PyTorch DataLoader expects as an input.

Under-the-hood, it performs a virtual inner join of the features of the underlying AnnData objects and thus allows to work with very large collections.

You can either perform a virtual inner join:

with collection.mapped(obs_keys=["cell_type"], join="inner") as dataset:
    print(len(dataset.var_joint))

749

Or a virtual outer join:

dataset = collection.mapped(obs_keys=["cell_type"], join="outer")

len(dataset.var_joint)

36503

This is compatible with a PyTorch DataLoader because it implements __getitem__ over a list of backed AnnData objects. The 5th cell in the collection can be accessed like:

dataset[5]

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{'X': array([0., 0., 0., ..., 0., 0., 0.], dtype=float32),
 '_store_idx': 0,
 'cell_type': 16}

The labels are encoded into integers:

dataset.encoders

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{'cell_type': {'B cell, CD19-positive': 0,
  'CD14-positive, CD16-negative classical monocyte': 1,
  'CD16-negative, CD56-bright natural killer cell, human': 2,
  'CD16-positive, CD56-dim natural killer cell, human': 3,
  'CD38-high pre-BCR positive cell': 4,
  'CD38-positive naive B cell': 5,
  'CD4-positive helper T cell': 6,
  'CD8-positive, CD25-positive, alpha-beta regulatory T cell': 7,
  'CD8-positive, alpha-beta memory T cell': 8,
  'CD8-positive, alpha-beta memory T cell, CD45RO-positive': 9,
  'T follicular helper cell': 10,
  'alpha-beta T cell': 11,
  'alveolar macrophage': 12,
  'animal cell': 13,
  'classical monocyte': 14,
  'conventional dendritic cell': 15,
  'cytotoxic T cell': 16,
  'dendritic cell': 17,
  'dendritic cell, human': 18,
  'effector memory CD4-positive, alpha-beta T cell': 19,
  'effector memory CD4-positive, alpha-beta T cell, terminally differentiated': 20,
  'effector memory CD8-positive, alpha-beta T cell, terminally differentiated': 21,
  'gamma-delta T cell': 22,
  'germinal center B cell': 23,
  'group 3 innate lymphoid cell': 24,
  'lymphocyte': 25,
  'macrophage': 26,
  'mast cell': 27,
  'megakaryocyte': 28,
  'memory B cell': 29,
  'mucosal invariant T cell': 30,
  'naive B cell': 31,
  'naive thymus-derived CD4-positive, alpha-beta T cell': 32,
  'naive thymus-derived CD8-positive, alpha-beta T cell': 33,
  'non-classical monocyte': 34,
  'plasma cell': 35,
  'plasmablast': 36,
  'plasmacytoid dendritic cell': 37,
  'progenitor cell': 38,
  'regulatory T cell': 39}}

Create a pytorch DataLoader

Let us use a weighted sampler:

from torch.utils.data import DataLoader, WeightedRandomSampler

# label_key for weight doesn't have to be in labels on init
sampler = WeightedRandomSampler(
    weights=dataset.get_label_weights("cell_type"), num_samples=len(dataset)
)
dataloader = DataLoader(dataset, batch_size=128, sampler=sampler)

We can now iterate through the data loader:

for batch in dataloader:
    pass

Close the connections in MappedCollection:

dataset.close()

In practice, use a context manager

with collection.mapped(obs_keys=["cell_type"]) as dataset:
    sampler = WeightedRandomSampler(
        weights=dataset.get_label_weights("cell_type"), num_samples=len(dataset)
    )
    dataloader = DataLoader(dataset, batch_size=128, sampler=sampler)
    for batch in dataloader:
        pass