Files
cellxgene/backend/common/compute/diffexp_generic.py
Severiano Badajoz 28b526b3fc feat: diffexp returns two genesets (#2230)
* feat: return two lists for diffexp (#2221)

* sp

* split out derive sort order, tests passing

* sp

* return diff exp results in two lists

* update

* copy implementation over to desktop

* add tests for two lists

* small fixes to complete backend implementation

* accept new diffexp response

* map diff exp response to genesets

* delete )

* name diffexp genesets with population names

* take constants out of state and allow width prop to override

* shorten mini-histo properly truncate and resize depending on expansion

* prepend new genesets

* rename data within diffexp action

* backend

* move diffexp ttest to common code module, update tests

* update for unit tests

* reference actual var

Co-authored-by: Madison Dunitz <madison.dunitz@chanzuckerberg.com>
Co-authored-by: Madison Dunitz <dunitzm@gmail.com>
2021-06-08 21:02:19 +00:00

143 lines
5.4 KiB
Python

import numpy as np
from scipy import sparse, stats
def diffexp_ttest(adaptor, maskA, maskB, top_n=8, diffexp_lfc_cutoff=0.01):
"""
Return differential expression statistics for top N variables.
Algorithm:
- compute log fold change (log2(meanA/meanB))
- compute Welch's t-test statistic and pvalue (w/ Bonferroni correction)
- return top N abs(logfoldchange) where lfc > diffexp_lfc_cutoff
If there are not N which meet criteria, augment by removing the logfoldchange
threshold requirement.
Notes on alogrithm:
- Welch's ttest provides basic statistics test.
https://en.wikipedia.org/wiki/Welch%27s_t-test
- p-values adjusted with Bonferroni correction.
https://en.wikipedia.org/wiki/Bonferroni_correction
:param adaptor: DataAdaptor instance
:param maskA: observation selection mask for set 1
:param maskB: observation selection mask for set 2
:param top_n: number of variables to return stats for
:param diffexp_lfc_cutoff: minimum
absolute value returning [ varindex, logfoldchange, pval, pval_adj ] for top N genes
:return: for top N genes, {"positive": for top N genes, [ varindex, logfoldchange, pval, pval_adj ], "negative": for top N genes, [ varindex, logfoldchange, pval, pval_adj ]}
"""
dataA = adaptor.get_X_array(maskA, None)
dataB = adaptor.get_X_array(maskB, None)
# mean, variance, N - calculate for both selections
meanA, vA, nA = mean_var_n(dataA)
meanB, vB, nB = mean_var_n(dataB)
res = diffexp_ttest_from_mean_var(meanA, vA, nA, meanB, vB, nB, top_n, diffexp_lfc_cutoff)
return res
def diffexp_ttest_from_mean_var(meanA, varA, nA, meanB, varB, nB, top_n, diffexp_lfc_cutoff):
n_var = meanA.shape[0]
top_n = min(top_n, n_var)
# variance / N
vnA = varA / min(nA, nB) # overestimate variance, would normally be nA
vnB = varB / min(nA, nB) # overestimate variance, would normally be nB
sum_vn = vnA + vnB
# degrees of freedom for Welch's t-test
with np.errstate(divide="ignore", invalid="ignore"):
dof = sum_vn ** 2 / (vnA ** 2 / (nA - 1) + vnB ** 2 / (nB - 1))
dof[np.isnan(dof)] = 1
# Welch's t-test score calculation
with np.errstate(divide="ignore", invalid="ignore"):
tscores = (meanA - meanB) / np.sqrt(sum_vn)
tscores[np.isnan(tscores)] = 0
# p-value
pvals = stats.t.sf(np.abs(tscores), dof) * 2
pvals_adj = pvals * n_var
pvals_adj[pvals_adj > 1] = 1 # cap adjusted p-value at 1
# logfoldchanges: log2(meanA / meanB)
logfoldchanges = np.log2(np.abs((meanA + 1e-9) / (meanB + 1e-9)))
stats_to_sort = tscores
# find all with lfc > cutoff
lfc_above_cutoff_idx = np.nonzero(np.abs(logfoldchanges) > diffexp_lfc_cutoff)[0]
# derive sort order
if lfc_above_cutoff_idx.shape[0] > top_n*2:
# partition top N
rel_t_partition = np.argpartition(stats_to_sort[lfc_above_cutoff_idx], (top_n, -top_n))
rel_t_partition_top_n = np.concatenate((rel_t_partition[-top_n:], rel_t_partition[:top_n]))
t_partition = lfc_above_cutoff_idx[rel_t_partition_top_n]
# sort the top N partition
rel_sort_order = np.argsort(stats_to_sort[t_partition])[::-1]
sort_order = t_partition[rel_sort_order]
else:
# partition and sort top N, ignoring lfc cutoff
partition = np.argpartition(stats_to_sort, (top_n, -top_n))
partition_top_n = np.concatenate((partition[-top_n:], partition[:top_n]))
rel_sort_order = np.argsort(stats_to_sort[partition_top_n])[::-1]
indices = np.indices(stats_to_sort.shape)[0]
sort_order = indices[partition_top_n][rel_sort_order]
# top n slice based upon sort order
logfoldchanges_top_n = logfoldchanges[sort_order]
pvals_top_n = pvals[sort_order]
pvals_adj_top_n = pvals_adj[sort_order]
# varIndex, logfoldchange, pval, pval_adj
result = {"positive": [[sort_order[i], logfoldchanges_top_n[i], pvals_top_n[i], pvals_adj_top_n[i]] for i in
range(top_n)],
"negative": [[sort_order[i], logfoldchanges_top_n[i], pvals_top_n[i], pvals_adj_top_n[i]] for i in
range(-1, -1 - top_n, -1)], }
return result
# Convenience function which handles sparse data
def mean_var_n(X):
"""
Two-pass variance calculation. Numerically (more) stable
than naive methods (and same method used by numpy.var())
https://en.wikipedia.org/wiki/Algorithms_for_calculating_variance#Two-pass
"""
# fp_err_occurred is a flag indicating that a floating point error
# occured somewhere in our compute. Used to trigger non-finite
# number handling.
fp_err_occurred = False
def fp_err_set(err, flag):
nonlocal fp_err_occurred
fp_err_occurred = True
with np.errstate(divide="call", invalid="call", call=fp_err_set):
n = X.shape[0]
if sparse.issparse(X):
mean = X.mean(axis=0).A1
dfm = X - mean
sumsq = np.sum(np.multiply(dfm, dfm), axis=0).A1
v = sumsq / (n - 1)
else:
mean = X.mean(axis=0)
dfm = X - mean
sumsq = np.sum(np.multiply(dfm, dfm), axis=0)
v = sumsq / (n - 1)
if fp_err_occurred:
mean[np.isfinite(mean) == False] = 0 # noqa: E712
v[np.isfinite(v) == False] = 0 # noqa: E712
else:
mean[np.isnan(mean)] = 0
v[np.isnan(v)] = 0
return mean, v, n