コード例 #1
0
def main(args):

    total_start_time = time.time()

    print('\n>> CLI Parameters ...\n')

    print(args)

    check_args(args)

    feature_file_format = os.path.splitext(args.outputNucleiFeatureFile)[1]

    if np.all(np.array(args.analysis_roi) == -1):
        process_whole_image = True
    else:
        process_whole_image = False

    #
    # Initiate Dask client
    #
    print('\n>> Creating Dask client ...\n')

    start_time = time.time()

    c = cli_utils.create_dask_client(args)

    print(c)

    dask_setup_time = time.time() - start_time
    print('Dask setup time = {} seconds'.format(dask_setup_time))

    #
    # Read Input Image
    #
    print('\n>> Reading input image ... \n')

    ts = large_image.getTileSource(args.inputImageFile)

    ts_metadata = ts.getMetadata()

    print(json.dumps(ts_metadata, indent=2))

    is_wsi = ts_metadata['magnification'] is not None

    #
    # Compute tissue/foreground mask at low-res for whole slide images
    #
    if is_wsi and process_whole_image:

        print('\n>> Computing tissue/foreground mask at low-res ...\n')

        start_time = time.time()

        im_fgnd_mask_lres, fgnd_seg_scale = \
            cli_utils.segment_wsi_foreground_at_low_res(ts)

        fgnd_time = time.time() - start_time

        print('low-res foreground mask computation time = {}'.format(
            cli_utils.disp_time_hms(fgnd_time)))

    #
    # Compute foreground fraction of tiles in parallel using Dask
    #
    tile_fgnd_frac_list = [1.0]

    it_kwargs = {
        'tile_size': {
            'width': args.analysis_tile_size
        },
        'scale': {
            'magnification': args.analysis_mag
        },
    }

    if not process_whole_image:

        it_kwargs['region'] = {
            'left': args.analysis_roi[0],
            'top': args.analysis_roi[1],
            'width': args.analysis_roi[2],
            'height': args.analysis_roi[3],
            'units': 'base_pixels'
        }

    if is_wsi:

        print('\n>> Computing foreground fraction of all tiles ...\n')

        start_time = time.time()

        num_tiles = ts.getSingleTile(**it_kwargs)['iterator_range']['position']

        print('Number of tiles = {}'.format(num_tiles))

        if process_whole_image:

            tile_fgnd_frac_list = htk_utils.compute_tile_foreground_fraction(
                args.inputImageFile, im_fgnd_mask_lres, fgnd_seg_scale,
                it_kwargs)

        else:

            tile_fgnd_frac_list = [1.0] * num_tiles

        num_fgnd_tiles = np.count_nonzero(
            tile_fgnd_frac_list >= args.min_fgnd_frac)

        percent_fgnd_tiles = 100.0 * num_fgnd_tiles / num_tiles

        fgnd_frac_comp_time = time.time() - start_time

        print('Number of foreground tiles = {0:d} ((1:2f)%%)'.format(
            num_fgnd_tiles, percent_fgnd_tiles))

        print('Tile foreground fraction computation time = {}'.format(
            cli_utils.disp_time_hms(fgnd_frac_comp_time)))

    #
    # Compute reinhard stats for color normalization
    #
    src_mu_lab = None
    src_sigma_lab = None

    if is_wsi and process_whole_image:

        print('\n>> Computing reinhard color normalization stats ...\n')

        start_time = time.time()

        src_mu_lab, src_sigma_lab = htk_cnorm.reinhard_stats(
            args.inputImageFile, 0.01, magnification=args.analysis_mag)

        rstats_time = time.time() - start_time

        print('Reinhard stats computation time = {}'.format(
            cli_utils.disp_time_hms(rstats_time)))

    #
    # Detect and compute nuclei features in parallel using Dask
    #
    print('\n>> Detecting nuclei and computing features ...\n')

    start_time = time.time()

    tile_result_list = []

    for tile in ts.tileIterator(**it_kwargs):

        tile_position = tile['tile_position']['position']

        if is_wsi and tile_fgnd_frac_list[tile_position] <= args.min_fgnd_frac:
            continue

        # detect nuclei
        cur_result = dask.delayed(compute_tile_nuclei_features)(
            args.inputImageFile, tile_position, args, it_kwargs, src_mu_lab,
            src_sigma_lab)

        # append result to list
        tile_result_list.append(cur_result)

    tile_result_list = dask.delayed(tile_result_list).compute()

    nuclei_annot_list = [
        annot for annot_list, fdata in tile_result_list for annot in annot_list
    ]

    nuclei_fdata = pd.concat([fdata for annot_list, fdata in tile_result_list],
                             ignore_index=True)

    nuclei_detection_time = time.time() - start_time

    print('Number of nuclei = {}'.format(len(nuclei_annot_list)))
    print('Nuclei detection time = {}'.format(
        cli_utils.disp_time_hms(nuclei_detection_time)))

    #
    # Write annotation file
    #
    print('\n>> Writing annotation file ...\n')

    annot_fname = os.path.splitext(
        os.path.basename(args.outputNucleiAnnotationFile))[0]

    annotation = {
        "name": annot_fname + '-nuclei-' + args.nuclei_annotation_format,
        "elements": nuclei_annot_list
    }

    with open(args.outputNucleiAnnotationFile, 'w') as annotation_file:
        json.dump(annotation, annotation_file, indent=2, sort_keys=False)

    #
    # Create CSV Feature file
    #
    print('>> Writing CSV feature file')

    if feature_file_format == '.csv':

        nuclei_fdata.to_csv(args.outputNucleiFeatureFile, index=False)

    elif feature_file_format == '.h5':

        nuclei_fdata.to_hdf(args.outputNucleiFeatureFile,
                            'Features',
                            format='table',
                            mode='w')

    else:

        raise ValueError(
            'Extension of output feature file must be .csv or .h5')

    total_time_taken = time.time() - total_start_time

    print('Total analysis time = {}'.format(
        cli_utils.disp_time_hms(total_time_taken)))
コード例 #2
0
ファイル: NucleiDetection.py プロジェクト: sskram/HistomicsTK
def main(args):

    total_start_time = time.time()

    print('\n>> CLI Parameters ...\n')

    print(args)

    if not os.path.isfile(args.inputImageFile):
        raise IOError('Input image file does not exist.')

    if len(args.reference_mu_lab) != 3:
        raise ValueError('Reference Mean LAB should be a 3 element vector.')

    if len(args.reference_std_lab) != 3:
        raise ValueError('Reference Stddev LAB should be a 3 element vector.')

    if len(args.analysis_roi) != 4:
        raise ValueError('Analysis ROI must be a vector of 4 elements.')

    if np.all(np.array(args.analysis_roi) == -1):
        process_whole_image = True
    else:
        process_whole_image = False

    #
    # Initiate Dask client
    #
    print('\n>> Creating Dask client ...\n')

    start_time = time.time()

    c = cli_utils.create_dask_client(args)

    print(c)

    dask_setup_time = time.time() - start_time
    print('Dask setup time = {}'.format(
        cli_utils.disp_time_hms(dask_setup_time)))

    #
    # Read Input Image
    #
    print('\n>> Reading input image ... \n')

    ts = large_image.getTileSource(args.inputImageFile)

    ts_metadata = ts.getMetadata()

    print(json.dumps(ts_metadata, indent=2))

    is_wsi = ts_metadata['magnification'] is not None

    #
    # Compute tissue/foreground mask at low-res for whole slide images
    #
    if is_wsi and process_whole_image:

        print('\n>> Computing tissue/foreground mask at low-res ...\n')

        start_time = time.time()

        im_fgnd_mask_lres, fgnd_seg_scale = \
            cli_utils.segment_wsi_foreground_at_low_res(ts)

        fgnd_time = time.time() - start_time

        print('low-res foreground mask computation time = {}'.format(
            cli_utils.disp_time_hms(fgnd_time)))

    #
    # Compute foreground fraction of tiles in parallel using Dask
    #
    tile_fgnd_frac_list = [1.0]

    it_kwargs = {
        'tile_size': {
            'width': args.analysis_tile_size
        },
        'scale': {
            'magnification': args.analysis_mag
        },
    }

    if not process_whole_image:

        it_kwargs['region'] = {
            'left': args.analysis_roi[0],
            'top': args.analysis_roi[1],
            'width': args.analysis_roi[2],
            'height': args.analysis_roi[3],
            'units': 'base_pixels'
        }

    if is_wsi:

        print('\n>> Computing foreground fraction of all tiles ...\n')

        start_time = time.time()

        num_tiles = ts.getSingleTile(**it_kwargs)['iterator_range']['position']

        print('Number of tiles = {}'.format(num_tiles))

        if process_whole_image:

            tile_fgnd_frac_list = htk_utils.compute_tile_foreground_fraction(
                args.inputImageFile, im_fgnd_mask_lres, fgnd_seg_scale,
                **it_kwargs)

        else:

            tile_fgnd_frac_list = np.full(num_tiles, 1.0)

        num_fgnd_tiles = np.count_nonzero(
            tile_fgnd_frac_list >= args.min_fgnd_frac)

        percent_fgnd_tiles = 100.0 * num_fgnd_tiles / num_tiles

        fgnd_frac_comp_time = time.time() - start_time

        print('Number of foreground tiles = {0:d} ({1:2f}%%)'.format(
            num_fgnd_tiles, percent_fgnd_tiles))

        print('Tile foreground fraction computation time = {}'.format(
            cli_utils.disp_time_hms(fgnd_frac_comp_time)))

    #
    # Compute reinhard stats for color normalization
    #
    src_mu_lab = None
    src_sigma_lab = None

    if is_wsi and process_whole_image:

        print('\n>> Computing reinhard color normalization stats ...\n')

        start_time = time.time()

        src_mu_lab, src_sigma_lab = htk_cnorm.reinhard_stats(
            args.inputImageFile, 0.01, magnification=args.analysis_mag)

        rstats_time = time.time() - start_time

        print('Reinhard stats computation time = {}'.format(
            cli_utils.disp_time_hms(rstats_time)))

    #
    # Detect nuclei in parallel using Dask
    #
    print('\n>> Detecting nuclei ...\n')

    start_time = time.time()

    tile_nuclei_list = []

    for tile in ts.tileIterator(**it_kwargs):

        tile_position = tile['tile_position']['position']

        if is_wsi and tile_fgnd_frac_list[tile_position] <= args.min_fgnd_frac:
            continue

        # detect nuclei
        cur_nuclei_list = dask.delayed(detect_tile_nuclei)(args.inputImageFile,
                                                           tile_position, args,
                                                           it_kwargs,
                                                           src_mu_lab,
                                                           src_sigma_lab)

        # append result to list
        tile_nuclei_list.append(cur_nuclei_list)

    tile_nuclei_list = dask.delayed(tile_nuclei_list).compute()

    nuclei_list = list(itertools.chain.from_iterable(tile_nuclei_list))

    nuclei_detection_time = time.time() - start_time

    print('Number of nuclei = {}'.format(len(nuclei_list)))

    print('Nuclei detection time = {}'.format(
        cli_utils.disp_time_hms(nuclei_detection_time)))

    #
    # Write annotation file
    #
    print('\n>> Writing annotation file ...\n')

    annot_fname = os.path.splitext(
        os.path.basename(args.outputNucleiAnnotationFile))[0]

    annotation = {
        "name": annot_fname + '-nuclei-' + args.nuclei_annotation_format,
        "elements": nuclei_list
    }

    with open(args.outputNucleiAnnotationFile, 'w') as annotation_file:
        json.dump(annotation, annotation_file, indent=2, sort_keys=False)

    total_time_taken = time.time() - total_start_time

    print('Total analysis time = {}'.format(
        cli_utils.disp_time_hms(total_time_taken)))