Source code for bmtk.builder.bionet.swc_reader

import os
import re
from collections import namedtuple
import numpy as np
import pandas as pd
from neuron import h

from bmtk.simulator.bionet import nrn

SegmentProps = namedtuple('SegmentProps', ['type', 'area', 'x', 'dist', 'length', 'dist0', 'dist1', 'sec_id'])
SegmentCoords = namedtuple('SegmentCoords', ['p0', 'p1', 'p05'])

[docs]def rotation_matrix(axis, theta): """Return the rotation matrix associated with counterclockwise rotation about the given axis by theta radians. """ axis = np.asarray(axis) theta = np.asarray(theta) axis = axis/np.sqrt(, axis)) a = np.cos(theta/2.0) b, c, d = -axis*np.sin(theta/2.0) aa, bb, cc, dd = a*a, b*b, c*c, d*d bc, ad, ac, ab, bd, cd = b*c, a*d, a*c, a*b, b*d, c*d return np.array([ [aa+bb-cc-dd, 2*(bc+ad), 2*(bd-ac)], [2*(bc-ad), aa+cc-bb-dd, 2*(cd+ab)], [2*(bd+ac), 2*(cd-ab), aa+dd-bb-cc] ])
[docs]class SWCReader(object): sec_type_swc = { 'soma': 1, 'somatic': 1, 'axon': 2, 'axonal': 2, 'dend': 3, 'basal': 3, 'apic': 4, 'apical': 4 } def __init__(self, swc_path, rng_seed=None): nrn.load_neuron_modules(None, None) self.swc_path = swc_path self.hobj = h.Biophys1(swc_path) self.rng_seed = rng_seed self._prng = np.random.RandomState(self.rng_seed) self._sections = None self._n_sections = None self._soma_pos = None self._seg_props = None self._seg_coords = None self._nseg = None self._swc_map = None self._axon_fixed = False self._axon_deleted = False def _copy(self): new_swc = SWCReader(swc_path=self.swc_path, rng_seed=self.rng_seed) if self._axon_fixed: new_swc.fix_axon() if self._axon_deleted: new_swc.delete_axon() return new_swc @property def sections(self): if self._sections is None: self._sections = [] for sec in self.hobj.all: self._sections.append(sec) return self._sections @property def n_sections(self): if self._n_sections is None: self._n_sections = len(self.sections) return self._n_sections @property def seg_props(self): if self._seg_props is None: seg_type = [] seg_area = [] seg_x = [] seg_dist = [] seg_length = [] seg_sec_id = [] h.distance(sec=self.hobj.soma[0]) # measure distance relative to the soma # for sec in self.hobj.all: for sec_id, sec in enumerate(self.sections): fullsecname = sec_type = fullsecname.split(".")[1][:4] # get sec name type without the cell name sec_type_swc = self.sec_type_swc[sec_type] # convert to swc code for seg in sec: seg_area.append(h.area(seg.x)) seg_x.append(seg.x) seg_length.append(sec.L / sec.nseg) seg_type.append(sec_type_swc) # record section type in a list # seg_dist.append(h.distance(seg.x)) # distance to the center of the segment seg_dist.append(h.distance(seg)) seg_sec_id.append(sec_id) length_arr = np.array(seg_length) dist_arr = np.array(seg_dist) dist0_arr = dist_arr - length_arr/2.0 dist1_arr = dist_arr + length_arr/2.0 self._seg_props = SegmentProps( type=np.array(seg_type), area=np.array(seg_area), x=np.array(seg_x), dist=dist_arr, length=length_arr, dist0=dist0_arr, dist1=dist1_arr, sec_id=np.array(seg_sec_id) ) return self._seg_props @property def seg_coords(self): if self._seg_coords is None: ix = 0 # segment index p0 = np.zeros((3, self.nseg)) # hold the coordinates of segment starting points p1 = np.zeros((3, self.nseg)) # hold the coordinates of segment end points p05 = np.zeros((3, self.nseg)) # for sec in self.hobj.all: for sec in self.sections: n3d = int(h.n3d(sec=sec)) # get number of n3d points in each section p3d = np.zeros((3, n3d)) # to hold locations of 3D morphology for the current section l3d = np.zeros(n3d) # to hold locations of 3D morphology for the current section diam3d = np.zeros(n3d) # to diameters for i in range(n3d): p3d[0, i] = h.x3d(i, sec=sec) # - p3dsoma[0] p3d[1, i] = h.y3d(i, sec=sec) # - p3dsoma[1] # shift coordinates such to place soma at the origin. p3d[2, i] = h.z3d(i, sec=sec) # - p3dsoma[2] diam3d[i] = h.diam3d(i, sec=sec) l3d[i] = h.arc3d(i, sec=sec) l3d /= sec.L # normalize nseg = sec.nseg l0 = np.zeros(nseg) # keep range of segment starting point l1 = np.zeros(nseg) # keep range of segment ending point l05 = np.zeros(nseg) for iseg, seg in enumerate(sec): l0[iseg] = seg.x - 0.5 * 1 / nseg # x (normalized distance along the section) for the beginning of the segment l1[iseg] = seg.x + 0.5 * 1 / nseg # x for the end of the segment l05[iseg] = seg.x p0[0, ix:ix + nseg] = np.interp(l0, l3d, p3d[0, :]) p0[1, ix:ix + nseg] = np.interp(l0, l3d, p3d[1, :]) p0[2, ix:ix + nseg] = np.interp(l0, l3d, p3d[2, :]) p1[0, ix:ix + nseg] = np.interp(l1, l3d, p3d[0, :]) p1[1, ix:ix + nseg] = np.interp(l1, l3d, p3d[1, :]) p1[2, ix:ix + nseg] = np.interp(l1, l3d, p3d[2, :]) p05[0, ix:ix + nseg] = np.interp(l05, l3d, p3d[0, :]) p05[1, ix:ix + nseg] = np.interp(l05, l3d, p3d[1, :]) p05[2, ix:ix + nseg] = np.interp(l05, l3d, p3d[2, :]) ix += nseg self._seg_coords = SegmentCoords(p0=p0, p1=p1, p05=p05) return self._seg_coords @property def nseg(self): if self._nseg is None: nseg = 0 for sec in self.hobj.all: nseg += sec.nseg # get the total # of segments in the cell self._nseg = nseg return self._nseg @property def soma_position(self): if self._soma_pos is None: n3dsoma = 0 r3dsoma = np.zeros(3) for sec in self.hobj.soma: n3d = int(h.n3d(sec=sec)) # get number of n3d points in each section # r3d = np.zeros((3, n3d)) # to hold locations of 3D morphology for the current section n3dsoma += n3d for i in range(n3d): r3dsoma[0] += h.x3d(i, sec=sec) r3dsoma[1] += h.y3d(i, sec=sec) r3dsoma[2] += h.z3d(i, sec=sec) r3dsoma /= n3dsoma self._soma_pos = r3dsoma return self._soma_pos @property def swc_map(self): if self._swc_map is None: swc_df = pd.read_csv(self.swc_path, sep=' ', names=['id', 'type', 'x', 'y', 'z', 'r', 'pid'], comment='#') swc_df = swc_df[['id', 'type']] name_indices = [] for ln in range(len(swc_df)): # in read_swc.hoc all non-bifurcating section of rows are assigned a global section-id. But for each # type (soma, dend, etc), there is also a nameindex id which is unique within the type, used to assign # sections to their name. So lines with sec_id=10 may have nameindex=3 (Biophys1[0].dend[3]) sec_id = int([ln]) # swc_id = int( # swc_type = int([ln]) name_index = int( name_indices.append(name_index) swc_df['nameindex'] = name_indices self._swc_map = swc_df return self._swc_map """ @soma_position.setter def soma_position(self, coords): assert(len(coords) == 3) self.set_soma_position(coords[0], coords[1], coords[2]) def set_soma_position(self, x, y, z): new_soma_coords = np.array([x, y, z]) if self._soma_pos is not None and not np.allclose(new_soma_coords, self._soma_pos, equal_nan=True): # check if the coordinates are the same as before self._seg_coords = None self._soma_pos = new_soma_coords """
[docs] def get_section(self, section_idx): return self.sections[section_idx]
[docs] def fix_axon(self): """Removes and refixes axon""" axon_diams = [self.hobj.axon[0].diam, self.hobj.axon[0].diam] for sec in self.hobj.all: section_name =".")[1][:4] if section_name == 'axon': axon_diams[1] = sec.diam for sec in self.hobj.axon: h.delete_section(sec=sec) h.execute('create axon[2]', self.hobj) for index, sec in enumerate(self.hobj.axon): sec.L = 30 sec.diam = 1 self.hobj.axonal.append(sec=sec) self.hobj.all.append(sec=sec) # need to remove this comment self.hobj.axon[0].connect(self.hobj.soma[0], 1.0, 0) self.hobj.axon[1].connect(self.hobj.axon[0], 1.0, 0) h.define_shape() self._sections = None self._n_sections = None self._axon_fixed = True
[docs] def delete_axon(self): for sec in self.hobj.axon: h.delete_section(sec=sec) h.define_shape() self._sections = None self._n_sections = None self._axon_deleted = True
[docs] def set_segment_dl(self, dl): """Define number of segments in a cell""" if self._seg_coords is not None: raise RuntimeError('Unable to segment the morphology after coordinates have already been calculated') self._nseg = 0 for sec in self.hobj.all: sec.nseg = 1 + 2 * int(sec.L/(2*dl)) self._nseg += sec.nseg # get the total number of segments in the cell
[docs] def choose_sections(self, section_names, distance_range, n_sections=1): """Similar to find_sections, but will only N=n_section number of sections_ids/x values randomly selected (may return less if there aren't as many sections :param section_names: 'soma', 'dend', 'apic', 'axon' :param distance_range: [float, float]: distance range of sections from the soma, in um. :param n_sections: int: maximum number of sections to select :return: [int], [float]: A list of all section_ids and a list of all segment_x values (as defined by NEURON) that meet the given critera. """ secs, probs = self.find_sections(section_names, distance_range) secs_ix = self._prng.choice(secs, n_sections, p=probs) return self.seg_props.sec_id[secs_ix], self.seg_props.x[secs_ix]
[docs] def find_sections(self, section_names, distance_range): """Retrieves a list of sections ids and section x's given a section name/type (eg axon, soma, apic, dend) and the distance from the soma. :param section_names: 'soma', 'dend', 'apic', 'axon' :param distance_range: [float, float]: distance range of sections from the soma, in um. :return: [float], [float]: A list of all section_ids and a list of all segment_x values (as defined by NEURON) that meet the given critera. """ dmin, dmax = distance_range[0], distance_range[1] seg_d0 = self.seg_props.dist0 seg_d1 = self.seg_props.dist1 seg_length = self.seg_props.length seg_type = self.seg_props.type # Find the fractional overlap between the segment and the distance range: # this is done by finding the overlap between [d0,d1] and [dmin,dmax] # np.minimum(seg_d1,dmax) find the smaller of the two end locations # np.maximum(seg_d0,dmin) find the larger of the two start locations # np.maximum(0,overlap) is used to return zero when segments do not overlap # and then dividing by the segment length frac_overlap = np.maximum(0, (np.minimum(seg_d1, dmax) - np.maximum(seg_d0, dmin))) / seg_length ix_drange = np.where(frac_overlap > 0) # find indexes with non-zero overlap ix_labels = np.array([], for tar_sec_label in section_names: # find indexes within sec_labels sec_type = self.sec_type_swc[tar_sec_label] # get swc code for the section label ix_label = np.where(seg_type == sec_type) ix_labels = np.append(ix_labels, ix_label) # target segment indexes tar_seg_ix = np.intersect1d(ix_drange, ix_labels) # find intersection between indexes for range and labels tar_seg_length = seg_length[tar_seg_ix] * frac_overlap[tar_seg_ix] # weighted length of targeted segments tar_seg_prob = tar_seg_length / np.sum(tar_seg_length) # probability of targeting segments return tar_seg_ix, tar_seg_prob
[docs] def move_and_rotate(self, soma_coords=None, rotation_angles=None, inplace=False): old_seg_coords = self.seg_coords new_p0 = old_seg_coords.p0.copy() new_p1 = old_seg_coords.p1.copy() new_p05 = old_seg_coords.p05.copy() new_soma_pos = self.soma_position.copy() if rotation_angles is not None: assert(len(rotation_angles) == 3) # try to calc the euler rotation matrix around an arbitary point was causing problems, instead move coords # so the the soma center (p05[0]) is at the origin soma_pos_mat = new_soma_pos.reshape((3, 1)) new_p0 = new_p0 - soma_pos_mat new_p1 = new_p1 - soma_pos_mat new_p05 = new_p05 - soma_pos_mat rotx_mat = rotation_matrix([1, 0, 0], rotation_angles[0]) roty_mat = rotation_matrix([0, 1, 0], rotation_angles[1]) rotz_mat = rotation_matrix([0, 0, 1], rotation_angles[2]) rotxyz_mat =, new_p0 =, new_p0) + soma_pos_mat new_p1 =, new_p1) + soma_pos_mat new_p05 =, new_p05) + soma_pos_mat if soma_coords is not None: assert(len(soma_coords) == 3) soma_coords = soma_coords if isinstance(soma_coords, np.ndarray) else np.array(soma_coords) displacement = soma_coords - self.soma_position displacement = displacement.reshape((3, 1)) # Req to allow adding vector to matrix new_p0 += displacement new_p1 += displacement new_p05 += displacement new_soma_pos = soma_coords new_seg_coords = SegmentCoords(p0=new_p0, p1=new_p1, p05=new_p05) if inplace: self._seg_coords = new_seg_coords return self else: new_swc_reader = self._copy() new_swc_reader._seg_props = self.seg_props new_swc_reader._swc_map = self._swc_map new_swc_reader._nseg = self.nseg new_swc_reader._seg_coords = new_seg_coords new_swc_reader._soma_pos = new_soma_pos return new_swc_reader
[docs] def get_coords(self, sec_id, sec_x): segs_indices = np.argwhere(self.seg_props.sec_id == sec_id).flatten() dev = abs(sec_x - self.seg_props.x[segs_indices]) # Find segment closest to x position idx = np.argmin(dev) return self.seg_coords.p05[:, segs_indices][:, idx]
[docs] def get_swc_id(self, sec_id, sec_x): # use sec type and nameindex to find all rows in the swc that correspond to sec_id sec = self.sections[sec_id] sec_nameindex = self._get_sec_nameindex(sec) sec_type = self._get_sec_type(sec) filtered_swc = self.swc_map[(self.swc_map['type'] == sec_type) & (self.swc_map['nameindex'] == sec_nameindex)] swc_ids = filtered_swc['id'].values # use sec_x, a value between [0, 1], to estimate which swc_id/line to choose. # Note: At the moment it assumes each line in the swc is the same distance apart, making estimating the sec_x # location easy by the number it appears in the squence if len(swc_ids) == 1: return swc_ids[0], sec_x else: swc_place = np.max((0.0, sec_x*len(swc_ids) - 1.0)) swc_indx = int(np.ceil(swc_place)) swc_id = swc_ids[swc_indx] swc_dist = swc_indx - swc_place return swc_id, swc_dist
def _get_sec_type(self, sec): sec_name = sec.hname() sec_type_str = sec_name.split('.')[-1].split('[')[0] type_str = self.sec_type_swc[sec_type_str] return int(type_str) def _get_sec_nameindex(self, sec): sec_name = sec.hname() sec_type_name = sec_name.split('.')[-1] nameindex_str ='\[(\d+)\]', sec_type_name).group(1) return int(nameindex_str)
swc_cache = {}
[docs]def get_swc(cell, morphology_dir=None, use_cache=False, dL=None): cell_pop = cell.get('population', 'default') cell_node_id = cell['node_id'] if use_cache and cell_pop in swc_cache and cell_node_id in swc_cache[cell_pop]: return swc_cache[cell_pop][cell_node_id] swc_path = cell['morphology'] if morphology_dir: swc_path = os.path.join(morphology_dir, swc_path) if not os.path.exists(swc_path) and not swc_path.endswith('.swc'): swc_path += '.swc' if not os.path.exists(swc_path): raise ValueError('File {} does not exists.'.format(swc_path)) swc = SWCReader(swc_path) if dL: swc.set_segment_dl(dL) if cell.get('model_processing', 'NULL') == 'aibs_perisomatic': swc.fix_axon() if any([cn in cell for cn in ['x', 'y', 'z']]): soma_coords = [cell.get('x', 0.0), cell.get('y', 0.0), cell.get('z', 0.0)] else: soma_coords = None if any([cn in cell for cn in ['rotation_angle_xaxis', 'rotation_angle_yaxis', 'rotation_angle_zaxis']]): rotation_angles = [ cell.get('rotation_angle_xaxis', 0.0), cell.get('rotation_angle_yaxis', 0.0), cell.get('rotation_angle_zaxis', 0.0) ] else: rotation_angles = None swc = swc.move_and_rotate(soma_coords=soma_coords, rotation_angles=rotation_angles) if use_cache: if cell_pop not in swc_cache: swc_cache[cell_pop] = {} swc_cache[cell_pop][cell_node_id] = swc return swc