scanpy.pp.pca

scanpy.pp.pca(data, n_comps=None, *, layer=None, zero_center=True, svd_solver=None, chunked=False, chunk_size=None, random_state=0, return_info=False, mask_var=_empty, use_highly_variable=None, dtype='float32', key_added=None, copy=False)

Principal component analysis [Pedregosa et al., 2011].

Computes PCA coordinates, loadings and variance decomposition. Uses the following implementations (and defaults for svd_solver):

	ndarray, spmatrix, or sparray	dask.array.Array
chunked=False, zero_center=True	sklearn PCA ('arpack')	dense: dask-ml PCA[1] ('auto') sparse or svd_solver='covariance_eigh': custom implementation ('covariance_eigh')
chunked=False, zero_center=False	sklearn TruncatedSVD ('randomized')	dask-ml TruncatedSVD[2] ('tsqr')
chunked=True (zero_center ignored)	sklearn IncrementalPCA ('auto')	dask-ml IncrementalPCA[3] ('auto')

[1]

Consider svd_solver='covariance_eigh' to reduce memory usage (see dask/dask-ml#985).

[2]

This implementation can not handle sparse chunks, try manually densifying them.

[3]

This implementation densifies sparse chunks and therefore has increased memory usage.

Parameters:

data AnnData | ndarray | csr_matrix | csc_matrix

The (annotated) data matrix of shape n_obs × n_vars. Rows correspond to cells and columns to genes.

n_comps int | None (default: None)

Number of principal components to compute. Defaults to 50, or 1 - minimum dimension size of selected representation.

layer str | None (default: None)

If provided, which element of layers to use for PCA.

zero_center bool (default: True)

If True, compute (or approximate) PCA from covariance matrix. If False, performa a truncated SVD instead of PCA.

Our default PCA algorithms (see svd_solver) support implicit zero-centering, and therefore efficiently operating on sparse data.

svd_solver Union[Literal['auto', 'full', 'tsqr', 'randomized'], Literal['tsqr', 'randomized'], Literal['auto', 'full', 'randomized'], Literal['arpack', 'covariance_eigh'], Literal['arpack', 'randomized'], Literal['covariance_eigh'], None] (default: None)

SVD solver to use. See table above to see which solver class is used based on chunked and zero_center, as well as the default solver for each class when svd_solver=None.

Efficient computation of the principal components of a sparse matrix currently only works with the 'arpack’ or 'covariance_eigh’ solver.

None

Choose automatically based on solver class (see table above).

'arpack'

ARPACK wrapper in SciPy (svds()). Not available for dask arrays.

'covariance_eigh'

Classic eigendecomposition of the covariance matrix, suited for tall-and-skinny matrices. With dask, array must be CSR or dense and chunked as (N, adata.shape[1]).

'randomized'

Randomized algorithm from Halko et al. [2009]. For dask arrays, this will use svd_compressed().

'auto'

Choose automatically depending on the size of the problem: Will use 'full' for small shapes and 'randomized' for large shapes.

'tsqr'

“tall-and-skinny QR” algorithm from Benson et al. [2013]. Only available for dense dask arrays.

Changed in version 1.9.3: Default value changed from 'arpack' to None.

Changed in version 1.4.5: Default value changed from 'auto' to 'arpack'.

chunked bool (default: False)

If True, perform an incremental PCA on segments of chunk_size. Automatically zero centers and ignores settings of zero_center, random_seed and svd_solver. If False, perform a full PCA/truncated SVD (see svd_solver and zero_center). See table above for which solver class is used.

chunk_size int | None (default: None)

Number of observations to include in each chunk. Required if chunked=True was passed.

random_state int | RandomState | None (default: 0)

Change to use different initial states for the optimization.

return_info bool (default: False)

Only relevant when not passing an AnnData: see “Returns”.

mask_var ndarray[tuple[int, ...], dtype[bool]] | str | None | Empty (default: _empty)

To run only on a certain set of genes given by a boolean array or a string referring to an array in var. By default, uses .var['highly_variable'] if available, else everything.

use_highly_variable bool | None (default: None)

Whether to use highly variable genes only, stored in .var['highly_variable']. By default uses them if they have been determined beforehand.

Deprecated since version 1.10.0: Use mask_var instead

layer

Layer of adata to use as expression values.

dtype Union[dtype[Any], None, type[Any], _SupportsDType[dtype[Any]], str, tuple[Any, int], tuple[Any, SupportsIndex | Sequence[SupportsIndex]], list[Any], _DTypeDict, tuple[Any, Any]] (default: 'float32')

Numpy data type string to which to convert the result.

key_added str | None (default: None)

If not specified, the embedding is stored as obsm['X_pca'], the loadings as varm['PCs'], and the the parameters in uns['pca']. If specified, the embedding is stored as obsm[key_added], the loadings as varm[key_added], and the the parameters in uns[key_added].

copy bool (default: False)

If an AnnData is passed, determines whether a copy is returned. Is ignored otherwise.

Return type:

AnnData | ndarray | csr_matrix | csc_matrix | None

Returns:

If data is array-like and return_info=False was passed, this function returns the PCA representation of data as an array of the same type as the input array.

Otherwise, it returns None if copy=False, else an updated AnnData object. Sets the following fields:

.obsm['X_pca' | key_added]csr_matrix | csc_matrix | ndarray (shape (adata.n_obs, n_comps))

PCA representation of data.

.varm['PCs' | key_added]ndarray (shape (adata.n_vars, n_comps))

The principal components containing the loadings.

.uns['pca' | key_added]['variance_ratio']ndarray (shape (n_comps,))

Ratio of explained variance.

.uns['pca' | key_added]['variance']ndarray (shape (n_comps,))

Explained variance, equivalent to the eigenvalues of the covariance matrix.