scanpy.queries.enrich#
- scanpy.queries.enrich(container, *, org='hsapiens', gprofiler_kwargs=mappingproxy({}))[source]#
Get enrichment for DE results.
This is a thin convenience wrapper around the very useful gprofiler.
This method dispatches on the first argument, leading to the following two signatures:
enrich(container, ...) enrich(adata: AnnData, group, key: str, ...)
Where:
enrich(adata, group, key, ...) = enrich(adata.uns[key]["names"][group], ...)
- Parameters:
- container
Iterable
[str
] |Mapping
[str
,Iterable
[str
]] Contains list of genes you’d like to search. If container is a
dict
all enrichment queries are made at once.- adata
AnnData object whose group will be looked for.
- group
The group whose genes should be used for enrichment.
- key
Key in
uns
to find group under.- org
str
(default:'hsapiens'
) Organism to query. Must be an organism in ensembl biomart. “hsapiens”, “mmusculus”, “drerio”, etc.
- gprofiler_kwargs
Mapping
[str
,Any
] (default:mappingproxy({})
) Keyword arguments to pass to
GProfiler.profile
, see gprofiler. Some useful options areno_evidences=False
which reports gene intersections,sources=['GO:BP']
which limits gene sets to only GO biological processes andall_results=True
which returns all results including the non-significant ones.- **kwargs
All other keyword arguments are passed to
sc.get.rank_genes_groups_df
. E.g. pval_cutoff, log2fc_min.
- container
- Return type:
- Returns:
Dataframe of enrichment results.
Examples
Using
sc.queries.enrich
on a list of genes:>>> import scanpy as sc >>> sc.queries.enrich(['KLF4', 'PAX5', 'SOX2', 'NANOG'], org="hsapiens") >>> sc.queries.enrich({'set1':['KLF4', 'PAX5'], 'set2':['SOX2', 'NANOG']}, org="hsapiens")
Using
sc.queries.enrich
on ananndata.AnnData
object:>>> pbmcs = sc.datasets.pbmc68k_reduced() >>> sc.tl.rank_genes_groups(pbmcs, "bulk_labels") >>> sc.queries.enrich(pbmcs, "CD34+")