def main():
basedir = os.path.join(this_dir, "../../datasets/LSM700_63x_sigb")
if not USE_CACHE_PLOTS:
cell_df = pd.read_hdf(os.path.join(basedir, "single_cell_data.h5"),
"cells")
file_df = filedb.get_filedb(os.path.join(basedir, "file_list.tsv"))
else:
file_df = None
cell_df = None
time = 48
location = "center"
slice_srt, slice_end = 5, 7 #10, 15
#slice_srt, slice_end = 5, 6 #10, 15 #
# There is no major difference between 5-6 and 7-8, just the QP skew is bigger in 5-6
#slice_srt, slice_end = 7, 8 #10, 15
# Moving to 2um because it makes the plots look nicer.
# fig, ax = plt.subplots(4, 2)
# axhisto = ax[:, 1]
# aximage = ax[:, 0]
fig, ax = plt.subplots(2, 4)
axhisto = ax[1, :]
aximage = ax[0, :]
for i, (name, path, roi, chans) in enumerate(image_list):
impath = os.path.join(image_base_dir, path)
aximage[i] = subfig_draw_bin.get_figure(aximage[i],
name,
impath,
roi,
chans,
FP_max_min,
(slice_srt, slice_end),
add_scale_bar=i == 0)
aximage[i].set_title("")
aximage[i].text(imgletter_lab[0],
imgletter_lab[1],
topletters[i],
transform=aximage[i].transAxes,
**letter_settings,
color="white")
text_x = 0.40
text_top = 0.85
line_sep = 0.15
title_loc, cv_loc, samp_loc, cell_loc = [
(text_x, text_top - (line_sep * i)) for i in range(4)
]
strain_map, des_strain_map = strainmap.load()
gchan = "green_raw_bg_meannorm"
rchan = "red_raw_bg_meannorm"
if not USE_CACHE_PLOTS:
cell_df = cell_df[cell_df[rchan] > 0].copy()
#max_val = 30000
#max_val = 1.0 #6.0 #20000
#gmax_val = 1.0 #7.5
max_val = 6.5 #2.5
gmax_val = 6.5 #0.75
nbins = 150
rbins = (0, max_val, nbins)
gbins = (0, gmax_val, nbins)
percentile = 0 #99
list_of_histos = [("wt_sigar_sigby", rchan, "WT P$_{sigA}$-RFP",
figure_util.strain_color["JLB021"]),
("wt_sigar_sigby", gchan, "WT P$_{sigB}$-YFP",
figure_util.strain_color["JLB021"]),
("delqp_sigar_sigby", gchan, "ΔrsbQP P$_{sigB}$-YFP",
figure_util.strain_color["JLB039"]),
("delru_sigar_sigby", gchan, "ΔrsbRU P$_{sigB}$-YFP",
figure_util.strain_color["JLB088"])]
print("-----------")
for i, (strain, chan, label, color) in enumerate(list_of_histos):
print(label)
strain_df = None
if not USE_CACHE_PLOTS:
fids = file_df[(file_df["time"] == time)
& (file_df["location"] == location) &
(file_df["strain"] == des_strain_map[strain])].index
strain_df = cell_df[cell_df["global_file_id"].isin(fids)]
dset = time, location, strain
plot_args = {"color": color, "max_min": "std", "mode_mean": False}
tbins = gbins
if "red" in chan:
tbins = rbins
args = (axhisto[i], strain_df, chan, tbins, (slice_srt, slice_end),
dset, percentile, USE_CACHE_PLOTS, this_dir, plot_args)
axhisto[i], _, meandmed = subfig_indivfile_histo.get_figure(*args)
axhisto[i].text(1.0,
hisletter_lab[1],
label,
horizontalalignment='right',
verticalalignment='top',
color="black",
fontsize=plt.rcParams["axes.titlesize"],
transform=axhisto[i].transAxes)
axhisto[i].text(hisletter_lab[0],
hisletter_lab[1],
letters[i],
transform=axhisto[i].transAxes,
**letter_settings)
#leg = axhisto[0].legend(loc="center right")
#axhisto[-1].set_xlabel("Mean normalised cell fluorecence")
axhisto[0].set_ylabel("Percentage of cells")
axhisto[0].set_xlim(0, max_val)
for a in np.ravel(axhisto):
#a.set_ylabel("Percentage of cells")
a.set_xlabel("Mean normalised cell fluorecence")
a.set_ylim(0, 5)
a.set_xlim(0, gmax_val)
a.tick_params(axis='x', which='both',
direction='out') #, length=2, pad=0)
a.tick_params(axis='y', which='both',
direction='out') #, length=2, pad=0)
# for a in axhisto[:-1]:
# a.set_xticklabels([])
for a in axhisto[1:]:
a.set_yticklabels([])
filename = "demo_longtail"
#fig.subplots_adjust(left=000, ri0ht=0.98, top = 1.0, bottom=0.06, hspace=0.08, wspace=0.2)
#width, height = figure_util.get_figsize(figure_util.fig_width_small_pt, wf=1.0, hf=1.7)
fig.subplots_adjust(left=0.05,
right=0.99,
top=1.0,
bottom=0.10,
hspace=0.08,
wspace=0.15)
width, height = figure_util.get_figsize(figure_util.fig_width_big_pt,
wf=1.0,
hf=0.5)
fig.set_size_inches(width, height)
figure_util.save_figures(fig, filename, ["png", "pdf"], this_dir)
# "cr_max":10000,
# "cg_min":2000,
# "cg_max":(2**14), }]
# height = 260 * 20
# width = 700 * 20
# i = files[0]
# spimg_ax = subfig_spore_image.plot_big_image(spimg_ax,
# sp_image_basedir + i["Path"],
# this_dir, # cache path.
# ((i["y"], i["y"] + height),
# (i["x"], i["x"] + width)),
# (height, width),
# i, vertical=False, scalebar=True)
# letter_lab = (-0.10, 0.98)
# for l, a in zip(figure_util.letters, [spimg_ax, spcount_ax, cellcount_ax]):
# a.text(letter_lab[0], letter_lab[1], l, transform=a.transAxes, fontsize=figure_util.letter_font_size)
filename = "spore_grad_density_compare"
width, height = figure_util.get_figsize(figure_util.fig_width_small_pt,
wf=1.0,
hf=1.1)
fig.subplots_adjust(left=0.1, right=0.95, top=0.98, bottom=0.09,
hspace=0.35) #, wspace=0.25)
fig.set_size_inches(width, height)
figure_util.save_figures(fig, filename, ["pdf", "png"],
os.path.dirname(__file__))
# print("request size : ", figure_util.inch2cm((width, height)))
# fig.savefig(filename + ".png", dpi=dpi)
# fig.savefig(filename + ".pdf", dpi=dpi)
# figure_util.print_pdf_size(filename + ".pdf")
letter_settings = {
"horizontalalignment": "center",
"verticalalignment": "top",
"fontsize": figure_util.letter_font_size,
"color": "black",
}
x1 = 0.02
aximg.text(x1, 0.995, "B", transform=figall.transFigure, **letter_settings)
aximg.text(x1, 0.64, "C", transform=figall.transFigure, **letter_settings)
aximg.text(x1, 0.50, "D", transform=figall.transFigure, **letter_settings)
aximg.text(x1, 0.36, "E", transform=figall.transFigure, **letter_settings)
aximg.text(x1, 0.22, "F", transform=figall.transFigure, **letter_settings)
x2 = 0.53
aximg.text(x2, 0.64, "G", transform=figall.transFigure, **letter_settings)
aximg.text(x2, 0.50, "H", transform=figall.transFigure, **letter_settings)
aximg.text(x2, 0.36, "I", transform=figall.transFigure, **letter_settings)
aximg.text(x2, 0.22, "J", transform=figall.transFigure, **letter_settings)
filename = "pad_movie_tracemain"
width, height = figure_util.get_figsize(figure_util.fig_width_small_pt,
wf=1.0,
hf=1.0)
figall.set_size_inches(width, height)
figall.subplots_adjust(left=0.15, right=0.99, top=1.0, bottom=0.1)
# hspace=0.05)
print("request size : ", figure_util.inch2cm((width, height)))
figure_util.save_figures(figall, filename, ["png", "pdf"], this_dir)
##################
im = skimage.io.imread(os.path.join(this_dir, "delru_bf10_col2_strip.png"))
ax_fstrip.imshow(im, interpolation="bicubic")
ax_fstrip.grid(False)
ax_fstrip.axis("off")
axes = [ax_exprmt, ax_gradnt, ax_fstrip, ax_pulses]
letter_style = {
"verticalalignment": "top",
"horizontalalignment": "right",
"fontsize": figure_util.letter_font_size,
# "color": "red"
}
letter_x = 0.03
axes[0].text(letter_x, 0.995, "A", transform=fig.transFigure, **letter_style)
axes[1].text(0.47, 0.995, "B", transform=fig.transFigure, **letter_style)
axes[2].text(letter_x, 0.63, "C", transform=fig.transFigure, **letter_style)
axes[3].text(letter_x, 0.26, "D", transform=fig.transFigure, **letter_style)
filename = "bf_movie_main"
# width, height = figure_util.get_figsize(figure_util.fig_width_big_pt, wf=1.0, hf=0.5 )
width, height = figure_util.get_figsize(figure_util.fig_width_small_pt,
wf=1.0,
hf=1.3)
fig.subplots_adjust(left=0.095, right=0.97, top=0.97,
bottom=0.06) # , hspace=0.25, wspace=0.25)
fig.set_size_inches(width, height) # common.cm2inch(width, height))
figure_util.save_figures(fig, filename, ["png", "pdf"], base_dir=this_dir)
def main():
curve_score_methods = {
"std":
("Standard deviation", (0.0, 1.0), lambda d, h, b: np.std(d)), # 1.5,
"mean": ("Mean", (0.0, 4.0), lambda d, h, b: np.mean(d)),
"cv": (
"Coefficient of variation",
(0.3, 0.8),
lambda d, h, b: scipy.stats.variation(d),
),
# "skew": ("modern skew",
# 0.0, 3.0,
# lambda d, h, b: scipy.stats.skew(d)),
"skew_normed": (
"Skew",
(0.0, 2.9),
lambda d, h, b: scipy.stats.skew(d, bias=False),
),
# "mode": ("Mode",
# 0.0, 3.5,
# lambda d, h, b: b[h.argmax()]),
# "num": ("# cells",
# 0.0, 2000,
# lambda d, h, b: len(d)),
# "pearson_mode_mean": ("pearson Mode mean",
# 0.0, 1.2,
# joy_plots_of_gradients.pearson_mode_mean_skew),
# "non_parameteric_skew": ("Non parameteric",
# 0.0, 0.4,
# joy_plots_of_gradients.non_parametric_skew),
"kurtosis":
("Kurtosis", (0.0, 8.0), lambda d, h, b: scipy.stats.kurtosis(d)),
}
plot_colors = [ # "mean",
# "std",
"cv",
# "skew",
# "num",
# "skew_normed",
"skew_normed", # same as pandas
# "pearson_mode_mean",
# "non_parameteric_skew",
# "kurtosis",
]
# basedir = "../../data/bio_film_data/63xdatasets"
#this_dir = os.path.dirname(__file__)
this_dir = "/media/nmurphy/BF_Data_Orange/"
#basedir = os.path.join(this_dir, "../../datasets/LSM700_63x_sigb")
basedir = os.path.join(this_dir, "datasets/LSM700_63x_sigb")
# cell_df = pd.read_hdf(os.path.join(basedir, "edge_redo_lh1segment_data_bg_back_bleed.h5"), "cells")
# cell_df = pd.read_hdf(os.path.join(basedir, "new_edge_bgsubv2_maxnorm_lh1segment.h5"), "cells")
cell_df = pd.read_hdf(os.path.join(basedir, "single_cell_data.h5"),
"cells")
# cell_df = pd.read_hdf(os.path.join(basedir, "edge_redo_lh1segment_data.h5"), "cells")
# cell_df = pd.read_hdf(os.path.join(basedir, "lh1segment_bgsub_data.h5"), "cells")
# cell_df = cell_df[cell_df["area"] > 140]
cell_df = cell_df[cell_df["distance"] > 2]
time = 48 # .0
location = "center"
file_df = filedb.get_filedb(os.path.join(basedir, "file_list.tsv"))
strain_map, des_strain_map = strainmap.load()
# cbar_mins = {0: 0.5, 1:0.0}
percentile = 0 # 99#
# green_chan = "meannorm_green"
# red_chan = "meannorm_red"
rmax = 6.5
gmax = 6.5 # 0.4
green_chan = "green_raw_bg_mean"
red_chan = "red_raw_bg_mean"
rmax = 50000
gmax = 10000
strains = [
("wt_sigar_sigby", red_chan, rmax, "WT\n P$_{sigA}$-RFP"),
("wt_sigar_sigby", green_chan, gmax, "WT\n P$_{\mathit{sigB}}$-YFP"),
(
"delru_sigar_sigby",
green_chan,
gmax,
"Δ$\mathit{rsbRU}$\n P$_{\mathit{sigB}}$-YFP",
),
(
"delqp_sigar_sigby",
green_chan,
gmax,
"Δ$\mathit{rsbQP}$\n P$_{\mathit{sigB}}$-YFP",
),
]
# ("2xqp_sigar_sigby", green_chan, gmax, "2$\\times$rsbQP\n P$_{sigB}$-YFP")]
fig, ax = plt.subplots(len(plot_colors), len(strains), sharey=True)
for c, (strain, chan, max_val, name) in enumerate(strains):
strain_num = des_strain_map[strain]
distances, sbins, histograms, stats = joy_plots_of_gradients.get_strain_result(
file_df,
cell_df,
time,
location,
strain_num,
chan,
max_val,
percentile,
curve_score_methods,
)
for r, k in enumerate(plot_colors):
color = figure_util.strain_color[strain_num.upper()]
ax[r, c], mv, leglist = joy_plots_of_gradients.plot_curves(
ax[r, c], color, distances, sbins, histograms, stats, k)
if c == len(strains) - 1:
posn = ax[r, c].get_position()
cbax = fig.add_axes([
posn.x0 + posn.width + 0.0005, posn.y0, 0.015, posn.height
])
label = curve_score_methods[k][0]
min_zval = curve_score_methods[k][1][0]
max_zval = curve_score_methods[k][1][1]
sm = plt.cm.ScalarMappable(
cmap=plt.get_cmap("viridis"),
norm=plt.Normalize(vmin=min_zval, vmax=max_zval),
)
sm._A = []
_ = plt.colorbar(sm, cax=cbax) # , fig=fig)
cbax.set_ylabel(label, rotation=-90, labelpad=8)
cbax.tick_params(direction="out")
if r == 0:
ax[r, c].set_title(name, fontsize=6)
ax[r, c].get_xaxis().set_ticklabels([])
ax[r, c].set_xlim(0, max_val)
# this didnt return the right mode for some reason
# leg = ax[0, -1].legend(leglist)
leg = ax[0, -1].legend(leglist, ["Mode", "Mean"],
loc="lower left",
bbox_to_anchor=(0.84, 0.97))
leg.set_zorder(400)
for a in ax.flatten():
a.tick_params(direction="out")
ax[0, 0].annotate(
"Distance from top of biofilm (μm)",
xy=(0, 0),
xytext=(0.02, 0.5),
textcoords="figure fraction",
# arrowprops=dict(facecolor='black', shrink=0.05),
horizontalalignment="center",
verticalalignment="center",
fontsize="medium",
color=mpl.rcParams["axes.labelcolor"],
rotation=90,
)
ax[1, 2].annotate(
"Normalized fluoresence",
xy=(0, 0),
xytext=(0.5, 0.04),
textcoords="figure fraction",
# arrowprops=dict(facecolor='black', shrink=0.05),
horizontalalignment="center",
verticalalignment="center",
fontsize="medium",
color=mpl.rcParams["axes.labelcolor"],
)
# for a in ax[:, 0].flatten():
# ticklabs = a.yaxis.get_ticklabels()
# ticklabs = a.get_yticks()#.tolist()
# ticklabs[-1] = ''
letters = ["A", "B", "C", "D", "E", "F", "G", "H", "I", "J"]
# letter_lab = (-0.13, 0.98)
for a, l in zip(ax.flatten(), letters):
a.annotate(
l,
xy=(0, 0),
xytext=(-0.13, 0.95),
textcoords="axes fraction",
# arrowprops=dict(facecolor='black', shrink=0.05),
horizontalalignment="center",
verticalalignment="center",
fontsize=figure_util.letter_font_size,
color="black",
)
# a.text(letter_lab[0], letter_lab[1], l, transform=a.transAxes, fontsize=8)
filename = "sup_meta_histo"
width, height = figure_util.get_figsize(figure_util.fig_width_medium_pt,
wf=1.0,
hf=0.6)
fig.subplots_adjust(left=0.085,
right=0.89,
top=0.89,
bottom=0.13,
hspace=0.20,
wspace=0.25)
fig.set_size_inches(width, height) # common.cm2inch(width, height))
figure_util.save_figures(fig, filename, ["png", "pdf"], this_dir)
def main():
basedir = os.path.join(this_dir, "../../datasets/LSM700_63x_sigb")
time = 48
location = "center"
# slice_srt, slice_end = 5, 7 #10, 15
slice_srt_end = (5, 7)
fig, ax = plt.subplots(2, 2)
axhisto = ax[1, 1]
aximage = [ax[0, 0], ax[0, 1], ax[1, 0]]
for i, (name, path, roi, chans) in enumerate(image_list):
impath = os.path.join(image_base_dir, path)
aximage[i] = subfig_draw_bin.get_figure(
aximage[i],
name,
impath,
roi,
chans,
FP_max_min,
slice_srt_end,
add_scale_bar=i == 0,
)
aximage[i].set_title("")
aximage[i].text(imgletter_lab[0],
imgletter_lab[1],
topletters[i],
transform=aximage[i].transAxes,
**letter_settings) # , color="white")
aximage[i].text(0.05,
0.05,
name,
transform=aximage[i].transAxes,
**label_settings,
color="white")
#####################
## Histograms
generate_data_subset = False
strain_map, des_strain_map = strainmap.load()
file_df = filedb.get_filedb(os.path.join(basedir, "file_list.tsv"))
cachedpath = os.path.join(basedir, "histo_tops_normed.h5")
gchan = "green_raw_bg_mean"
rchan = "red_raw_bg_mean"
nbins = 150
gmax = 1
gbins = np.linspace(0, gmax, nbins)
list_of_histos = [
# ("2xqp_sigar_sigby", gchan, rchan, gbins, slice_srt_end, "2xQP", strain_color["JLB095"]),
(
"wt_sigar_sigby",
gchan,
rchan,
gbins,
slice_srt_end,
r"WT P$_{\mathit{sigB}}$-YFP",
strain_color["JLB021"],
),
(
"delru_sigar_sigby",
gchan,
rchan,
gbins,
slice_srt_end,
r"Δ$\mathit{rsbRU}$ P$_{\mathit{sigB}}$-YFP",
strain_color["JLB088"],
),
(
"delqp_sigar_sigby",
gchan,
rchan,
gbins,
slice_srt_end,
r"Δ$\mathit{rsbQP}$ P$_{\mathit{sigB}}$-YFP",
strain_color["JLB039"],
),
]
axes = [axhisto] * len(list_of_histos)
if generate_data_subset:
df = pd.read_hdf(os.path.join(basedir, "single_cell_data.h5"), "cells")
cellsdf = subfig_normalised_histos.get_data_subset(
df, file_df, list_of_histos, time, location, cachedpath)
else:
cellsdf = pd.read_hdf(cachedpath, "cells")
axes = subfig_normalised_histos.get_figure(cellsdf, file_df, axes, time,
location, list_of_histos)
axes[0].legend()
axhisto.text(hisletter_lab[0],
hisletter_lab[1],
letters[0],
transform=axhisto.transAxes,
**letter_settings)
axhisto.set_ylabel("Percentage of cells")
axhisto.set_xlim(0, gmax)
axhisto.set_ylim(0, 8.5)
axhisto.tick_params(axis="x", which="both",
direction="out") # , length=2, pad=0)
axhisto.tick_params(axis="y", which="both",
direction="out") # , length=2, pad=0)
axhisto.yaxis.set_major_locator(mticker.MaxNLocator(nbins=3, integer=True))
axhisto.set_xlabel("Normalised cell fluorecence")
filename = "demo_longtail"
fig.subplots_adjust(left=0.05,
right=0.95,
top=0.99,
bottom=0.1,
hspace=0.08,
wspace=0.20)
width, height = figure_util.get_figsize(figure_util.fig_width_small_pt,
wf=1.0,
hf=0.9)
fig.set_size_inches(width, height)
figure_util.save_figures(fig, filename, ["png", "pdf"], this_dir)
def main():
this_dir = os.path.dirname(__file__)
basedir = os.path.join(this_dir, "../../datasets/LSM700_63x_sigb")
#cell_df = pd.read_hdf(os.path.join(basedir, "edge_redo_lh1segment_data_bg_back_bleed.h5"), "cells")
cell_df = pd.read_hdf(os.path.join(basedir, "single_cell_data.h5"), "cells")
print(cell_df.columns)
file_df = filedb.get_filedb(os.path.join(basedir, "file_list.tsv"))
file_df.loc[file_df["time"] == 26.0, ['time']] = 24.0
file_df.loc[file_df["time"] == 38.0, ['time']] = 36.0
USE_CACHE_PLOTS = False
time = 48
location = "center"
slice_srt, slice_end = 5, 7
fig, axhisto = plt.subplots(1, 1)
strain_map, des_strain_map = strainmap.load()
gchan = "green_raw_bg_autofluor_bleedthrough_meannorm"
gmax_val = 20
nbins=150
gbins = (0, gmax_val, nbins)
percentile = 0
list_of_histos = [
("wt_sigar_sigby", gchan, "WT P$_{sigB}$-YFP", strain_color["JLB021"]),
("delqp_sigar_sigby", gchan, "ΔrsbQP P$_{sigB}$-YFP", strain_color["JLB039"]),
("delru_sigar_sigby", gchan, "ΔrsbRU P$_{sigB}$-YFP", strain_color["JLB088"]),
("2xqp_sigar_sigby", gchan, "2$\\times$rsbQP P$_{sigB}$-YFP", strain_color["JLB095"]),
]
print("-----------")
lelines = []
lelabs = []
for i, (strain, chan, label, color) in enumerate(list_of_histos):
print(label)
fids = file_df[(file_df["time"] == time) &
(file_df["location"] == location) &
(file_df["strain"] == des_strain_map[strain])].index
strain_df = cell_df[cell_df["global_file_id"].isin(fids)]
#strain_df = get_strain(file_df, cell_df, strain)
plot_args = {"color":color, "max_min":"none", "mode_mean":False}
tbins = gbins
dset = time, location, strain
args = (axhisto, strain_df, chan, tbins, (slice_srt, slice_end), dset, percentile, USE_CACHE_PLOTS, this_dir, plot_args)
axhisto, line, _ = subfig_indivfile_histo.get_figure(*args)
lelines += [line]
lelabs += [label]
axhisto.legend(lelines, lelabs)
axhisto.set_xlabel("Normalised cell fluorecence (bleed through subtracted)")
axhisto.set_ylabel("Percentage of cells")
axhisto.set_ylim(0, 7)
axhisto.set_xlim(0, gmax_val)
filename = "sup_bleed_histo"
fig.subplots_adjust(left=0.1, right=0.9, top = 0.98, bottom=0.2)#, hspace=0.35, wspace=0.2)
width, height = figure_util.get_figsize(figure_util.fig_width_small_pt, wf=1.0, hf=0.5)
fig.set_size_inches(width, height)# common.cm2inch(width, height))
figure_util.save_figures(fig, filename, ["png", "pdf"], this_dir)