Implement driver class for scanpy

This commit is contained in:
Charlotte Weaver
2018-06-07 15:22:32 -07:00
parent 9cf300caeb
commit fabd3ca2ff
2 changed files with 96 additions and 57 deletions

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@@ -1,15 +1,23 @@
from abc import ABC, abstractmethod
from abc import ABCMeta, abstractmethod
class CXGDriver(metaclass=abc.ABCMeta):
class CXGDriver(metaclass=ABCMeta):
def __init__(self, data, schema=None, graph_method=None, diffexp_method=None):
self.data = _load_data(data)
self.data = self._load_data(data)
@abstractmethod
@staticmethod
def _load_data(data):
pass
@abstractmethod
def _load_or_infer_schema(data):
pass
@abstractmethod
def _set_cell_ids(self):
pass
@abstractmethod
def cells(self):
pass

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@@ -1,84 +1,115 @@
from os.path import join
import scanpy.api as sc
import numpy as np
from ..util.schema_parse import parse_schema
from ..driver import CXGDriver
class ScanpyEngine():
def __init__(self, dataloc):
self.ADATA = sc.read(join(dataloc, "data.h5ad"))
self.cell_count = self._cell_count
self.schema = parse_schema(join(dataloc, "data_schema.json"))
class ScanpyEngine(CXGDriver):
def _cell_count(self):
return len(self.ADATA.obs.index)
def __init__(self, data, schema=None, graph_method=None, diffexp_method=None):
self.data = self._load_data(data)
self.schema = self._load_or_infer_schema(schema)
self._set_cell_ids()
self.cell_count = self.data.shape[0]
# TODO Do I need this?
self.gene_count = self.data.shape[1]
self.graph_method = graph_method
self.diffexp_method = diffexp_method
def all_cells(self):
return self.ADATA.obs.index.tolist()
def all_genes(self):
return self.ADATA.var.index.tolist()
@staticmethod
def _load_data(data):
return sc.read(data)
def gene_count(self):
return len(self.ADATA.var.index)
def _load_or_infer_schema(schema):
data_schema = None
if not schema:
pass
else:
data_schema = parse_schema(schema)
return data_schema
def _set_cell_ids(self):
self.data.obs['cxg_cell_id'] = list(range(self.data.obs.shape[0]))
self.data.obs["cell_name"] = list(self.data.obs.index)
self.data.obs.set_index('cxg_cell_id', inplace=True)
def cells(self):
return list(self.data.obs.index)
def cellids(self):
return list(self.data.obs.index)
def genes(self):
return self.data.var.index.tolist()
def filter_cells(self, filter):
"""
Filter cells from data and return a subset of the data
:param filter:
:return: iterator through cell ids
"""
cell_idx = np.ones((self.cell_count(),), dtype=bool)
# TODO does this need to be a generator too?
for key, value in filter.items():
if value["variable_type"] == "categorical":
key_idx = np.in1d(getattr(self.ADATA.obs, key), value["query"])
key_idx = np.in1d(getattr(self.data.obs, key), value["query"])
cell_idx = np.logical_and(cell_idx, key_idx)
else:
min_ = value["query"]["min"]
max_ = value["query"]["max"]
if min_:
key_idx = np.array((getattr(self.ADATA.obs, key) >= min_).data)
key_idx = np.array((getattr(self.data.obs, key) >= min_).data)
cell_idx = np.logical_and(cell_idx, key_idx)
if max_:
key_idx = np.array((getattr(self.ADATA.obs, key) <= min_).data)
key_idx = np.array((getattr(self.data.obs, key) <= min_).data)
cell_idx = np.logical_and(cell_idx, key_idx)
return self.ADATA[cell_idx, :]
# If this is slow, could vectorize with logical array and then loop through that
for idx in self.cell_count:
if cell_idx[idx]:
yield self.data.obs['cxg_cell_id'][idx]
@staticmethod
def metadata_ranges(data, schema):
metadata_ranges = {}
for field in schema:
if schema[field]["variabletype"] == "categorical":
group_by = field
if group_by == "CellName":
group_by = 'index'
metadata_ranges[field] = {"options": data.obs.groupby(group_by).size().to_dict()}
else:
metadata_ranges[field] = {
"range": {
"min": data.obs[field].min(),
"max": data.obs[field].max()
}
}
return metadata_ranges
# Should this return the order of metadata fields as the first value?
def metadata(self, cells_iterator, fields=None):
"""
Generator for metadata. Gets the metadata values cell by cell and returns all value
or only certain values if names is not None
@staticmethod
def metadata(data):
cell_ids = []
metadata = data.obs.to_dict(orient="records")
# Do i have to loop twice?
for idx, cell_name in enumerate(data.obs.index):
metadata[idx]["CellName"] = cell_name
cell_ids.append(cell_name)
return metadata, cell_ids
:param cells_iterator: from filter cells, iterator for cellids
:param fields: list of keys for metadata to return, returns all metadata values if not set.
:return: Iterator for cellid + list of cells metadata values ex. [cell-id, val1, val2, val3]
"""
if not fields:
fields = self.data.obs.columns.tolist()
for cell_id in cells_iterator:
yield [cell_id] + self.data.obs.loc[cell_id, [fields]].tolist()
@staticmethod
# TODO cache this
# TODO accept n-dim versions too
# TODO allow optional kw params to function
def create_graph(data, graph_method="umap"):
# Run the graph method
getattr(sc.tl, graph_method)(data)
graph = data.obsm["X_{graph_method}".format(graph_method=graph_method)]
def create_graph(self, cells_iterator):
"""
Computes a n-d layout for cells through dimensionality reduction.
:param cells_iterator: from filter cells, iterator for cellids
:return: Iterator for [cellid-1, pos1, pos2], [cellid-2, pos1, pos2]
"""
cell_ids = list(cells_iterator)
getattr(sc.tl, self.graph_method)(self.data[self.data.obs.index.isin(cell_ids)])
graph = self.data.obsm["X_{graph_method}".format(graph_method=self.graph_method)]
normalized_graph = (graph - graph.min()) / (graph.max() - graph.min())
return np.hstack((data.obs.index.values.reshape(len(data.obs.index), 1), normalized_graph)).tolist()
for idx, cell_id in enumerate(cell_ids):
yield [cell_id] + normalized_graph[idx].tolist()
def diffexp(self, cells_iterator_1, cells_iterator_2):
"""
Computes the top differentially expressed genes between two clusters
:param cells_iterator_1: First set of cell ids
:param cells_iterator_2: Second set of cell ids
:return: Up in the air: I recommend [gene name, mean_expression_cells1, mean_expression_cells2, average_difference, statistic_value]
"""
pass