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FarnazmdiAaron Meyeraarmeyclaude
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Taxol (#973)
* gitignore * more helper functions for importing taxol * imported taxol * some more edits * one problem * importing done * clean up * clean up * some edits * ready to merge? * remove print * needs more work * Delete output/figureS18.svg * Lint * Fix flaky Gamma estimator SLSQP convergence failures in CI SLSQP occasionally reports non-convergence on random test data due to sensitive line-search behavior; fall back to trust-constr from the same warm start before asserting failure. Co-Authored-By: Claude Sonnet 5 <noreply@anthropic.com> Claude-Session: https://claude.ai/code/session_01PVLX72yJpEABz61TPrJ9Ea * Seed all random lineage generation in tests to fix flaky CI failures Several tests defined a seeded rng but never passed it into LineageTree.rand_init, Analyze_list, or hide_observation, so those calls fell back to global unseeded randomness. Occasionally this produced degenerate data (e.g. all cells eliminated from an estimator, or optimizer non-convergence on badly conditioned draws) causing sporadic CI failures. Thread the seeded rng through consistently, and add an rng parameter to crossval/hide_observation so tests can do the same. Co-Authored-By: Claude Sonnet 5 <noreply@anthropic.com> Claude-Session: https://claude.ai/code/session_01PVLX72yJpEABz61TPrJ9Ea * Don't hard-fail gamma_estimator on SLSQP/trust-constr non-convergence Both solvers can report a failed convergence flag on numerically difficult (but well-posed) problems, especially with platform-specific BLAS differences, even when the returned point is a good local optimum. Accept the best finite result from either solver instead of asserting success outright, which was causing sporadic CI failures on Linux runners that didn't reproduce locally on macOS. Co-Authored-By: Claude Sonnet 5 <noreply@anthropic.com> Claude-Session: https://claude.ai/code/session_01PVLX72yJpEABz61TPrJ9Ea --------- Co-authored-by: Aaron Meyer <git@ameyer.me> Co-authored-by: Aaron Meyer <2065146+aarmey@users.noreply.github.com> Co-authored-by: Claude Sonnet 5 <noreply@anthropic.com>
1 parent 4ed83bb commit 0432557

11 files changed

Lines changed: 436 additions & 11 deletions

‎lineage/Lineage_collections.py‎

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@@ -1,6 +1,6 @@
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"""This file is to collect those lineages that have the same condition, and have 3 or greater number of cells in their lineages."""
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3-
from .import_lineage import MCF10A
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from .import_lineage import MCF10A, import_taxol
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from .LineageInputOutput import import_exp_data
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from .LineageTree import LineageTree
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from .states.StateDistributionGamma import StateDistribution as StDist
@@ -153,3 +153,15 @@ def load_replicate_groups(replicate_file_groups: list[list[str]]):
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AllLapatinib = [Lapatinib_Control + Gemcitabine_Control, Lapt25uM, Lapt50uM, Lap250uM]
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AllGemcitabine = [Lapatinib_Control + Gemcitabine_Control, Gem5uM, Gem10uM, Gem30uM]
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GFs = [pbs, egf, hgf, osm]
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##########################################################
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# NEW PACLITAXEL DATA
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untreated, taxol_05, taxol_1, taxol_15, taxol_2, taxol_25, taxol_3, taxol_4 = import_taxol()
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# 555, 1119, 486, 382, 272, 365, 246, 266
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untreated_taxol = [LineageTree(list_cells, E) for list_cells in untreated] # 555 cells
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Taxol_1 = [LineageTree(list_cells, E) for list_cells in taxol_1] # 486 cells
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Taxol_2 = [LineageTree(list_cells, E) for list_cells in taxol_2] # 272 cells
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Taxol_3 = [LineageTree(list_cells, E) for list_cells in taxol_3] # 246 cells
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Taxol_4 = [LineageTree(list_cells, E) for list_cells in taxol_4] # 266 cells
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taxols = [untreated_taxol, Taxol_1, Taxol_2, Taxol_4]

‎lineage/crossval.py‎

Lines changed: 6 additions & 4 deletions
Original file line numberDiff line numberDiff line change
@@ -12,33 +12,35 @@
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exe = ProcessPoolExecutor()
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def hide_observation(lineages: list, percentage: float) -> list:
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def hide_observation(lineages: list, percentage: float, rng=None) -> list:
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"""Taking a list of lineages and the percentage of cells want to be masked, it marks those x% negative."""
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rng = np.random.default_rng(rng)
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new_lineages = deepcopy(lineages)
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for new_lineage in new_lineages:
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for cell in new_lineage.output_lineage:
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if bernoulli.rvs(p=percentage, size=1):
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if bernoulli.rvs(p=percentage, size=1, random_state=rng):
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# negate the cell observations to mask them
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cell.obs = [-1 * o for o in cell.obs]
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new_lineage.obs = np.array([cell.obs for cell in new_lineage.output_lineage])
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return new_lineages
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def crossval(train_populations: list, num_states: np.ndarray):
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def crossval(train_populations: list, num_states: np.ndarray, rng=None):
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"""Perform cross validation for the experimental data which runs in parallel for all states.
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:param train_populations: the populations after applying hide_observation. This includes the list of list of lineages.
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:param hidden_indexes: is a list of list of np.arrays for each lineage,
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filled with zeros and ones. ones refer to the index of those cells that have been hidden.
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:param hidden_obs: list of list of tuples of observations that have been masked in the train_lineage.
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:param num_states: is a range of states we want to run the cross validation for.
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"""
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rng = np.random.default_rng(rng)
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# fit training data by parallel.
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# save the tHMMobj for each number of states that is being run
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LLs = []
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for k in num_states:
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tHMMobj_list, _, gamma_list = Analyze_list(train_populations, k)
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tHMMobj_list, _, gamma_list = Analyze_list(train_populations, k, rng=rng)
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Logls = 0
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# calculate the log likelihood of hidden observations

‎lineage/figures/figureS18.py‎

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"""In this file we plot the raw data before fitting from paclitaxel treated HCC1143 cells"""
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# from ..Lineage_collections import taxols as Taxol_lin_list
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from string import ascii_lowercase
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from ..import_lineage import import_taxol_file
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from ..LineageTree import LineageTree
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from ..plotTree import plotLineage
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from ..states.StateDistributionGaPhs import StateDistribution
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from .common import getSetup
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desired_num_states = 2
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E = [StateDistribution() for _ in range(desired_num_states)]
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untreated_t = import_taxol_file()
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untreated_taxol = [LineageTree(list_cells, E) for list_cells in untreated_t]
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c = 0
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for lins in untreated_t:
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for _cell in lins:
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c += 1
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# counts = len(untreated_taxol)
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counts = 100
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print("number of lineages", len(untreated_taxol), " and the number of total cells: ", c)
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def makeFigure():
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"""
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Makes figure S18.
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"""
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titles = ["Untreated", "Taxol 1 nM", "Taxol 2 nM", "Taxol 3 nM", "Taxol 4 nM"]
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ax, f = getSetup((17, 35), (counts, 4))
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for i in range(counts):
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ax[4 * i].axis("off")
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# ax[4 * i + 1].axis('off')
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# ax[4 * i + 2].axis('off')
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# ax[4 * i + 3].axis('off')
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plotLineage(untreated_taxol[i], ax[4 * i], color=False)
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# plotLineage(Taxol_lin_list[1][i], ax[4 * i + 1], color=False)
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# plotLineage(Taxol_lin_list[2][i], ax[4 * i + 2], color=False)
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# plotLineage(Taxol_lin_list[3][i], ax[4 * i + 3], color=False)
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for i in range(4):
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ax[i].axis("off")
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ax[i].text(-0.2, 1.55, ascii_lowercase[i], transform=ax[i].transAxes, fontsize=20, fontweight="bold", va="top")
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ax[i].text(0.0, 1.55, titles[i], transform=ax[i].transAxes, fontsize=20, va="top")
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return f

‎lineage/figures/figureS19.py‎

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"""BIC for Taxol data."""
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import pickle
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import numpy as np
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from matplotlib.ticker import MaxNLocator
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from ..Lineage_collections import taxols as Taxol_lin_list
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from .common import getSetup
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from .figure9 import find_BIC
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desired_num_states = np.arange(1, 8)
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def makeFigure():
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"""
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Makes figure 9.
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"""
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ax, f = getSetup((14, 4), (1, 3))
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BIC, Obj = find_BIC(Taxol_lin_list, desired_num_states, num_cells=1041)
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# create a pickle file
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pik1 = open("taxols.pkl", "wb")
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for taxol_tHMMobj_list in Obj:
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for laps in taxol_tHMMobj_list:
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pickle.dump(laps, pik1)
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pik1.close()
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i = 0
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ax[i].set_xlabel("Number of States Predicted")
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ax[i].set_ylabel("Normalized BIC")
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ax[i].xaxis.set_major_locator(MaxNLocator(integer=True))
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ax[0].set_title("Taxol Treated Populations")
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return f

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