scanpy.pp.highly_variable_genes
- scanpy.pp.highly_variable_genes(adata, layer=None, n_top_genes=None, min_disp=0.5, max_disp=inf, min_mean=0.0125, max_mean=3, span=0.3, n_bins=20, flavor='seurat', subset=False, inplace=True, batch_key=None, check_values=True)
Annotate highly variable genes [Satija15] [Zheng17] [Stuart19].
Expects logarithmized data, except when
flavor='seurat_v3'
, in which count data is expected.Depending on
flavor
, this reproduces the R-implementations of Seurat [Satija15], Cell Ranger [Zheng17], and Seurat v3 [Stuart19].For the dispersion-based methods ([Satija15] and [Zheng17]), the normalized dispersion is obtained by scaling with the mean and standard deviation of the dispersions for genes falling into a given bin for mean expression of genes. This means that for each bin of mean expression, highly variable genes are selected.
For [Stuart19], a normalized variance for each gene is computed. First, the data are standardized (i.e., z-score normalization per feature) with a regularized standard deviation. Next, the normalized variance is computed as the variance of each gene after the transformation. Genes are ranked by the normalized variance.
See also
scanpy.experimental.pp._highly_variable_genes
for additional flavours (e.g. Pearson residuals).- Parameters:
- adata : AnnData
The annotated data matrix of shape
n_obs
×n_vars
. Rows correspond to cells and columns to genes.- layer : str | None (default:
None
) If provided, use
adata.layers[layer]
for expression values instead ofadata.X
.- n_top_genes : int | None (default:
None
) Number of highly-variable genes to keep. Mandatory if
flavor='seurat_v3'
.- min_mean : float | None (default:
0.0125
) If
n_top_genes
unequalsNone
, this and all other cutoffs for the means and the normalized dispersions are ignored. Ignored ifflavor='seurat_v3'
.- max_mean : float | None (default:
3
) If
n_top_genes
unequalsNone
, this and all other cutoffs for the means and the normalized dispersions are ignored. Ignored ifflavor='seurat_v3'
.- min_disp : float | None (default:
0.5
) If
n_top_genes
unequalsNone
, this and all other cutoffs for the means and the normalized dispersions are ignored. Ignored ifflavor='seurat_v3'
.- max_disp : float | None (default:
inf
) If
n_top_genes
unequalsNone
, this and all other cutoffs for the means and the normalized dispersions are ignored. Ignored ifflavor='seurat_v3'
.- span : float (default:
0.3
) The fraction of the data (cells) used when estimating the variance in the loess model fit if
flavor='seurat_v3'
.- n_bins : int (default:
20
) Number of bins for binning the mean gene expression. Normalization is done with respect to each bin. If just a single gene falls into a bin, the normalized dispersion is artificially set to 1. You’ll be informed about this if you set
settings.verbosity = 4
.- flavor : Literal[‘seurat’, ‘cell_ranger’, ‘seurat_v3’] (default:
'seurat'
) Choose the flavor for identifying highly variable genes. For the dispersion based methods in their default workflows, Seurat passes the cutoffs whereas Cell Ranger passes
n_top_genes
.- subset : bool (default:
False
) Inplace subset to highly-variable genes if
True
otherwise merely indicate highly variable genes.- inplace : bool (default:
True
) Whether to place calculated metrics in
.var
or return them.- batch_key : Optional[str] (default:
None
) If specified, highly-variable genes are selected within each batch separately and merged. This simple process avoids the selection of batch-specific genes and acts as a lightweight batch correction method. For all flavors, genes are first sorted by how many batches they are a HVG. For dispersion-based flavors ties are broken by normalized dispersion. If
flavor = 'seurat_v3'
, ties are broken by the median (across batches) rank based on within-batch normalized variance.- check_values : bool (default:
True
) Check if counts in selected layer are integers. A Warning is returned if set to True. Only used if
flavor='seurat_v3'
.
- Return type:
Optional[pd.DataFrame]
- Returns:
: Depending on
inplace
returns calculated metrics (DataFrame
) or updates.var
with the following fields- highly_variable
bool
boolean indicator of highly-variable genes
- means
means per gene
- dispersions
For dispersion-based flavors, dispersions per gene
- dispersions_norm
For dispersion-based flavors, normalized dispersions per gene
- variances
For
flavor='seurat_v3'
, variance per gene- variances_norm
For
flavor='seurat_v3'
, normalized variance per gene, averaged in the case of multiple batches- highly_variable_rank
float
For
flavor='seurat_v3'
, rank of the gene according to normalized variance, median rank in the case of multiple batches- highly_variable_nbatches
int
If batch_key is given, this denotes in how many batches genes are detected as HVG
- highly_variable_intersection
bool
If batch_key is given, this denotes the genes that are highly variable in all batches
- highly_variable
Notes
This function replaces
filter_genes_dispersion()
.