from abc import ABCMeta, abstractmethod """ Sort order for methods 1. Initialize 2. Helper 3. Filter 4. Data & Metadata 5. Computation """ class CXGDriver(metaclass=ABCMeta): def __init__(self, data, args): self.data = self._load_data(data) self.layout_method = args["layout"] self.diffexp_method = args["diffexp"] self.max_category_items = args["max_category_items"] self.cluster = None @property def features(self): features = { "cluster": {"available": False}, "layout": { "obs": {"available": False}, "var": {"available": False}, }, "diffexp": {"available": False} } # TODO - Interactive limit should be generated from the actual available methods see GH issue #94 if self.layout_method: # TODO handle "var" when gene layout becomes available features["layout"]["obs"] = {"available": True, "interactiveLimit": 50000} if self.diffexp_method: features["diffexp"] = {"available": True, "interactiveLimit": 50000} if self.cluster: features["cluster"] = {"available": True, "interactiveLimit": 50000} return features @staticmethod @abstractmethod def _load_data(data): pass @abstractmethod def filter_dataframe(self, filter): """ Filter cells from data and return a subset of the data. They can operate on both obs and var dimension with indexing and filtering by annotation value. Filters are combined with the and operator. See REST specs for info on filter format: https://github.com/chanzuckerberg/cellxgene/blob/master/docs/REST_API.md :param filter: dictionary with filter params :return: View into scanpy object with cells/genes filtered """ pass @abstractmethod def annotation(self, filter, axis, fields=None): """ Gets annotation value for each observation :param filter: filter: dictionary with filter params :param axis: string obs or var :param fields: list of keys for annotation to return, returns all annotation values if not set. :return: dict: names - list of fields in order, data - list of lists or metadata [observation ids, val1, val2...] """ pass @abstractmethod def data_frame(self, filter, axis): """ Retrieves data for each variable for observations in data frame :param filter: filter: dictionary with filter params :param axis: string obs or var :return: { "var": list of variable ids, "obs": [cellid, var1 expression, var2 expression, ...], } """ pass @abstractmethod def diffexp_topN(self, obsFilter1, obsFilter2, top_n=None, interactive_limit=None): """ Computes the top N differentially expressed variables between two observation sets. If mode is "TOP_N", then stats for the top N dataframes contain a subset of variables, then statistics for all variables will be returned, otherwise only the top N vars will be returned. :param obsFilter1: filter: dictionary with filter params for first set of observations :param obsFilter2: filter: dictionary with filter params for second set of observations :param top_n: Limit results to top N (Top var mode only) :param interactive_limit: -- don't compute if total # genes in dataframes are larger than this :return: top N genes and corresponding stats """ pass @abstractmethod def layout(self, filter, interactive_limit=None): """ Computes a n-d layout for cells through dimensionality reduction. :param filter: filter: dictionary with filter params :param interactive_limit: -- don't compute if total # genes in dataframes are larger than this :return: [cellid, x, y, ...] """ pass