openflexure-microscope-server/openflexure_microscope/api/default_extensions/scan.py
2020-01-06 17:55:43 +00:00

405 lines
12 KiB
Python

import itertools
import logging
import uuid
from typing import Tuple
from functools import reduce
from openflexure_microscope.camera.base import generate_basename
from openflexure_microscope.common.flask_labthings.find import (
find_device,
find_extension,
)
from openflexure_microscope.common.flask_labthings.extensions import BaseExtension
from openflexure_microscope.common.flask_labthings.views.tasks import TaskSchema
from openflexure_microscope.common.flask_labthings.decorators import (
marshal_with,
use_args,
)
from openflexure_microscope.common.flask_labthings import fields
from openflexure_microscope.devel import (
taskify,
abort,
update_task_progress,
)
from openflexure_microscope.common.flask_labthings.resource import Resource
import time
### Grid construction
def construct_grid(initial, step_sizes, n_steps, style="raster"):
"""
Given an initial position, step sizes, and number of steps,
construct a 2-dimensional list of scan x-y positions.
"""
arr = []
for i in range(n_steps[0]): # x axis
arr.append([])
for j in range(n_steps[1]): # y axis
# Create a coordinate array
coord = [initial[ax] + [i, j][ax] * step_sizes[ax] for ax in range(2)]
# Append coordinate array to position grid
arr[i].append(tuple(coord))
# Style modifiers
if style == "snake":
for i, line in enumerate(arr):
if i % 2 != 0:
line.reverse()
return arr
def flatten_grid(grid):
"""
Convert a 3D list of scan positions into a flat list
of sequential positions.
"""
grid = list(itertools.chain(*grid))
return grid
### Progress
_images_to_be_captured: int = 1
_images_captured_so_far: int = 0
def progress():
progress = (_images_captured_so_far / _images_to_be_captured) * 100
logging.info(progress)
return progress
### Capturing
def capture(
microscope,
basename,
scan_id,
temporary: bool = False,
use_video_port: bool = False,
resize: Tuple[int, int] = None,
bayer: bool = False,
metadata: dict = {},
tags: list = [],
):
# Construct a tile filename
filename = "{}_{}_{}_{}".format(basename, *microscope.stage.position)
folder = "SCAN_{}".format(basename)
# Create output object
output = microscope.camera.new_image(
temporary=temporary, filename=filename, folder=folder
)
# Capture
microscope.camera.capture(
output.file, use_video_port=use_video_port, resize=resize, bayer=bayer
)
# Affix metadata
if "scan" not in tags:
tags.append("scan")
# Inject system metadata
output.put_metadata(microscope.metadata, system=True)
# Insert custom metadata
output.put_metadata(metadata)
# Insert custom tags
output.put_tags(tags)
### Scanning
def tile(
microscope,
basename: str = None,
temporary: bool = False,
step_size: int = [2000, 1500, 100],
grid: list = [3, 3, 5],
style="raster",
autofocus_dz: int = 50,
use_video_port: bool = False,
resize: Tuple[int, int] = None,
bayer: bool = False,
fast_autofocus=False,
metadata: dict = {},
tags: list = [],
):
global _images_to_be_captured
global _images_captured_so_far
# Keep task progress
# TODO: Make this line not nasty
_images_to_be_captured = reduce((lambda x, y: x * y), grid)
_images_captured_so_far = 0
# Generate a basename if none given
if not basename:
basename = generate_basename()
# Generate a stack ID
scan_id = uuid.uuid4()
# Store initial position
initial_position = microscope.stage.position
# Add scan metadata
if "time" not in metadata:
metadata["time"] = generate_basename()
metadata.update(
{
"scan_id": scan_id,
"basename": basename,
"scan_parameters": {
"step_size": step_size,
"grid": grid,
"style": style,
"autofocus_dz": autofocus_dz,
},
}
)
# Check if autofocus is enabled
autofocus_extension = find_extension("autofocus")
if (
autofocus_dz
and autofocus_extension
and microscope.has_real_stage()
and microscope.has_real_camera()
):
autofocus_enabled = True
else:
autofocus_enabled = False
z_stack_dz = (
grid[2] * step_size[2] if grid[2] > 1 else 0
) # shorthand for Z stack range
# Construct an x-y grid (worry about z later)
x_y_grid = construct_grid(initial_position, step_size[:2], grid[:2], style=style)
# Keep the initial Z position the same as our current position
next_z = initial_position[2]
if fast_autofocus: # If fast autofocus is enabled, make
next_z += autofocus_dz / 2 # sure we start from the top of the range
initial_z = next_z # Save this value for use in raster scans
# Now step through each point in the x-y coordinate array
for line in x_y_grid:
# If rastering, rather than snake (or eventually spiral)
# Return focus to initial position
if style == "raster":
next_z = initial_z
logging.debug("Returning to initial z position")
microscope.stage.move_abs(
[line[0][0], line[0][1], next_z]
) # RWB: I think this line is redundant
for x_y in line:
# Move to new grid position without changing z
logging.debug("Moving to step {}".format([x_y[0], x_y[1], next_z]))
microscope.stage.move_abs([x_y[0], x_y[1], next_z])
# Refocus
if autofocus_enabled:
if fast_autofocus:
autofocus_extension.fast_autofocus(
dz=autofocus_dz,
target_z=-z_stack_dz / 2.0, # Finish below the focus
initial_move_up=False, # We're already at the top of the scan
)
# TODO: save the focus data for future reference? Use it for diagnostics?
else:
logging.debug("Running autofocus")
autofocus_extension.autofocus(
range(-3 * autofocus_dz, 4 * autofocus_dz, autofocus_dz)
)
logging.debug("Finished autofocus")
time.sleep(1) # TODO: Remove
# If we're not doing a z-stack, just capture
if grid[2] <= 1:
capture(
microscope,
basename,
scan_id,
temporary=temporary,
use_video_port=use_video_port,
resize=resize,
bayer=bayer,
metadata=metadata,
tags=tags,
)
# Update task progress
_images_captured_so_far += 1
update_task_progress(progress())
else:
logging.debug("Entering z-stack")
stack(
microscope=microscope,
basename=basename,
temporary=temporary,
scan_id=scan_id,
step_size=step_size[2],
steps=grid[2],
center=not fast_autofocus, # fast_autofocus does this for us!
return_to_start=not fast_autofocus,
use_video_port=use_video_port,
resize=resize,
bayer=bayer,
metadata=metadata,
tags=tags,
)
# Make sure we use our current best estimate of focus (i.e. the current position) next point
next_z = microscope.stage.position[2]
if fast_autofocus:
next_z += (
autofocus_dz / 2
) # Fast autofocus requires us to start at the top of the range
if grid[2] > 1:
next_z -= int(
grid[2] / 2.0 * step_size[2]
) # Z stacking means we're higher up to start with
logging.debug("Returning to {}".format(initial_position))
microscope.stage.move_abs(initial_position)
def stack(
microscope,
basename: str = None,
temporary: bool = False,
scan_id: str = None,
step_size: int = 100,
steps: int = 5,
center: bool = True,
return_to_start: bool = True,
use_video_port: bool = False,
resize: Tuple[int, int] = None,
bayer: bool = False,
metadata: dict = {},
tags: list = [],
):
global _images_captured_so_far
# Generate a basename if none given
if not basename:
basename = generate_basename()
# Generate a stack ID
if not scan_id:
scan_id = uuid.uuid4()
# Add scan metadata
if not "time" in metadata:
metadata["time"] = generate_basename()
# Store initial position
initial_position = microscope.stage.position
with microscope.lock:
# Move to center scan
if center:
logging.debug("Moving to starting position")
microscope.stage.move_rel([0, 0, int((-step_size * steps) / 2)])
for i in range(steps):
time.sleep(0.1)
logging.debug("Capturing...")
capture(
microscope,
basename,
scan_id,
temporary=temporary,
use_video_port=use_video_port,
resize=resize,
bayer=bayer,
metadata=metadata,
tags=tags,
)
# Update task progress
_images_captured_so_far += 1
update_task_progress(progress())
if i != steps - 1:
logging.debug("Moving z by {}".format(step_size))
microscope.stage.move_rel([0, 0, step_size])
if return_to_start:
logging.debug("Returning to {}".format(initial_position))
microscope.stage.move_abs(initial_position)
### Web views
class TileScanAPI(Resource):
@use_args(
{
"filename": fields.String(),
"temporary": fields.Boolean(missing=False),
"step_size": fields.List(fields.Integer, missing=[2000, 1500, 100]),
"grid": fields.List(fields.Integer, missing=[3, 3, 5]),
"style": fields.String(missing="raster"),
"autofocus_dz": fields.Integer(missing=50),
"fast_autofocus": fields.Boolean(missing=False),
"use_video_port": fields.Boolean(missing=False),
"bayer": fields.Boolean(missing=False),
"metadata": fields.Dict(missing={}),
"tags": fields.List(fields.String, missing=[]),
"resize": fields.Dict(missing=None), # TODO: Validate keys
}
)
@marshal_with(TaskSchema())
def post(self, args):
microscope = find_device("openflexure_microscope")
if not microscope:
abort(503, "No microscope connected. Unable to autofocus.")
resize = args.get("resize", None)
if resize:
if ("width" in resize) and ("height" in resize):
resize = (
int(resize["width"]),
int(resize["height"]),
) # Convert dict to tuple
else:
abort(404)
logging.info("Running tile scan...")
task = taskify(tile)(
microscope,
basename=args.get("filename"),
temporary=args.get("temporary"),
step_size=args.get("step_size"),
grid=args.get("grid"),
style=args.get("style"),
autofocus_dz=args.get("autofocus_dz"),
use_video_port=args.get("use_video_port"),
resize=resize,
bayer=args.get("bayer"),
fast_autofocus=args.get("fast_autofocus"),
metadata=args.get("metadata"),
tags=args.get("tags"),
)
# return a handle on the scan task
return task
scan_extension_v2 = BaseExtension("scan")
scan_extension_v2.add_view(TileScanAPI, "/tile")
scan_extension_v2.register_action(TileScanAPI)