import sys
import os
os.environ["OPENBLAS_NUM_THREADS"] = sys.argv[-2]
N = int(sys.argv[-2])
from os import listdir, mkdir
import numpy as np
import multiprocessing
from math import nan
from scipy.io import savemat
def chirpForMulti(invar):
model, sec_num, loc, filename = invar
if model == 'kole':
from getCells import KoleCell
cell, _ = KoleCell()
seg = cell.apic[sec_num](loc)
soma_seg = cell.soma(0.5)
if model == 'kolenoim':
from getCells import KoleCell
cell, _ = KoleCell()
from neuron import h
for sec in h.allsec():
try:
sec.uninsert('Km')
except:
pass
seg = cell.apic[sec_num](loc)
soma_seg = cell.soma(0.5)
elif model == 'neymotinkole':
from getCells import NeymotinKoleCell
cell = NeymotinKoleCell()
seg = cell.apic[sec_num](loc)
soma_seg = cell.soma(0.5)
elif model == 'neymotinharnett':
from getCells import NeymotinHarnettCell
cell = NeymotinHarnettCell()
seg = cell.apic[sec_num](loc)
soma_seg = cell.soma(0.5)
elif model == 'neymotinmigliore':
from getCells import NeymotinMiglioreCell
cell = NeymotinMiglioreCell()
seg = cell.apic[sec_num](loc)
soma_seg = cell.soma(0.5)
elif model == 'hay':
from getCells import HayCell
cell, _ = HayCell()
seg = cell.apic[sec_num](loc)
soma_seg = cell.soma[0](0.5)
elif model == 'ackerantic':
from getCells import AckerAnticCell
cell = AckerAnticCell()
seg = cell.apical[sec_num](loc)
soma_seg = cell.soma[0](0.5)
elif model == 'haymig':
from getCells import HayCellMig
cell, _ = HayCellMig()
seg = cell.apic[sec_num](loc)
soma_seg = cell.soma[0](0.5)
from chirpUtils import applyChirp, getChirp
amp = 0.025
f0, f1, t0, Fs, delay = 0.5, 10, 10, 1000, 5 # for looking at bimodal leading phase response in Hay cell
I, t = getChirp(f0, f1, t0, amp, Fs, delay)
print('running chirp on ' + str(seg))
applyChirp(I, t, seg, soma_seg, t0, delay, Fs, f1, out_file_name=filename)
print(str(sec) + ' ' + str(loc) + ': done')
#populate data tuple
data = []
models = ['kole', 'neymotinkole', 'neymotinharnett', 'neymotinmigliore', 'hay', 'ackerantic']
## handle each model accordingly
# for model in models:
model = sys.argv[-1]
if model == 'kole':
from getCells import KoleCell
cell, trunk = KoleCell()
for sec_num in trunk:
nseg = cell.apic[sec_num].nseg
if nseg == 1:
data.append([model, sec_num, 0.5, '/u/craig/L5PYR_Resonance/Kole/trunk_data/'+str(cell.apic[sec_num](0.5))])
else:
for loc in np.linspace(1/(nseg+1), nseg/(nseg+1), nseg):
data.append([model, sec_num, loc, '/u/craig/L5PYR_Resonance/Kole/trunk_data/'+str(cell.apic[sec_num](loc))])
if model == 'kolenoim':
from getCells import KoleCell
cell, trunk = KoleCell()
for sec_num in trunk:
nseg = cell.apic[sec_num].nseg
if nseg == 1:
data.append([model, sec_num, 0.5, '/u/craig/L5PYR_Resonance/Kole/noim_trunk_data/'+str(cell.apic[sec_num](0.5))])
else:
for loc in np.linspace(1/(nseg+1), nseg/(nseg+1), nseg):
data.append([model, sec_num, loc, '/u/craig/L5PYR_Resonance/Kole/noim_trunk_data/'+str(cell.apic[sec_num](loc))])
if model == 'neymotinkole':
from getCells import NeymotinKoleCell
cell = NeymotinKoleCell()
for sec_num, sec in enumerate(cell.apical_maintrunk):
nseg = sec.nseg
if nseg == 1:
data.append([model, sec_num, 0.5, '/u/craig/L5PYR_Resonance/Neymotin/kole_trunk_data/'+str(cell.apic[sec_num](0.5))])
else:
for loc in np.linspace(1/(nseg+1), nseg/(nseg+1), nseg):
data.append([model, sec_num, loc, '/u/craig/L5PYR_Resonance/Neymotin/kole_trunk_data/'+str(cell.apic[sec_num](loc))])
if model == 'neymotinharnett':
from getCells import NeymotinHarnettCell
cell = NeymotinHarnettCell()
for sec_num, sec in enumerate(cell.apical_maintrunk):
nseg = sec.nseg
if nseg == 1:
data.append([model, sec_num, 0.5, '/u/craig/L5PYR_Resonance/Neymotin/harnett_trunk_data/'+str(cell.apic[sec_num](0.5))])
else:
for loc in np.linspace(1/(nseg+1), nseg/(nseg+1), nseg):
data.append([model, sec_num, loc, '/u/craig/L5PYR_Resonance/Neymotin/harnett_trunk_data/'+str(cell.apic[sec_num](loc))])
if model == 'neymotinmigliore':
from getCells import NeymotinMiglioreCell
cell = NeymotinMiglioreCell()
for sec_num, sec in enumerate(cell.apical_maintrunk):
nseg = sec.nseg
if nseg == 1:
data.append([model, sec_num, 0.5, '/u/craig/L5PYR_Resonance/Neymotin/migliore_trunk_data/'+str(cell.apic[sec_num](0.5))])
else:
for loc in np.linspace(1/(nseg+1), nseg/(nseg+1), nseg):
data.append([model, sec_num, loc, '/u/craig/L5PYR_Resonance/Neymotin/migliore_trunk_data/'+str(cell.apic[sec_num](loc))])
if model == 'hay':
from getCells import HayCell
cell, trunk = HayCell()
for sec_num in trunk:
nseg = cell.apic[sec_num].nseg
if nseg == 1:
data.append([model, sec_num, 0.5, '/u/craig/L5PYR_Resonance/Hay/trunk_data/'+str(cell.apic[sec_num](0.5))])
else:
for loc in np.linspace(1/(nseg+1), nseg/(nseg+1), nseg):
data.append([model, sec_num, loc, '/u/craig/L5PYR_Resonance/Hay/trunk_data/'+str(cell.apic[sec_num](loc))])
if model == 'haymig':
from getCells import HayCellMig
cell, trunk = HayCellMig()
for sec_num in trunk:
nseg = cell.apic[sec_num].nseg
if nseg == 1:
data.append([model, sec_num, 0.5, '/u/craig/L5PYR_Resonance/Hay/mig_trunk_data/'+str(cell.apic[sec_num](0.5))])
else:
for loc in np.linspace(1/(nseg+1), nseg/(nseg+1), nseg):
data.append([model, sec_num, loc, '/u/craig/L5PYR_Resonance/Hay/mig_trunk_data/'+str(cell.apic[sec_num](loc))])
if model == 'ackerantic':
from getCells import AckerAnticCell
cell = AckerAnticCell()
for sec_num in cell.apical_maintrunk:
nseg = cell.apical[sec_num].nseg
if nseg == 1:
data.append([model, sec_num, 0.5, '/u/craig/L5PYR_Resonance/AckerAntic/trunk_data/'+str(cell.apical[sec_num](0.5))])
else:
for loc in np.linspace(1/(nseg+1), nseg/(nseg+1), nseg):
data.append([model, sec_num, loc, '/u/craig/L5PYR_Resonance/AckerAntic/trunk_data/'+str(cell.apical[sec_num](loc))])
data = tuple(data)
def mp_handler():
p = multiprocessing.Pool(N)
p.map(chirpForMulti, data)
if __name__ == '__main__':
mp_handler()