rodinia-benchmark/opencl/leukocyte/OpenCL/detect_main.c

#include "find_ellipse.h"
#include "track_ellipse.h"

// Global variables used by OpenCL functions
cl_context context;
cl_command_queue command_queue;
cl_device_id device;

int main(int argc, char ** argv) {
	
	// Make sure the command line arguments have been specified
	if (argc !=3)	{
		fprintf(stderr, "Usage: %s <input file> <number of frames to process>", argv[0]);
		exit(EXIT_FAILURE);
	}

	// Choose the best GPU in case there are multiple available
	choose_GPU();

	// Keep track of the start time of the program
	long long program_start_time = get_time();
	
	// Let the user specify the number of frames to process
	int num_frames = atoi(argv[2]);
	
	// Open video file
	char *video_file_name = argv[1];
	
	avi_t *cell_file = AVI_open_input_file(video_file_name, 1);
	if (cell_file == NULL)	{
		AVI_print_error("Error with AVI_open_input_file");
		exit(EXIT_FAILURE);
	}
	
	// Transfer precomputed constants to the GPU
	compute_constants();
	
	int i, j, *crow, *ccol, pair_counter = 0, x_result_len = 0, Iter = 20, ns = 4, k_count = 0, n;
	MAT *cellx, *celly, *A;
	double *GICOV_spots, *t, *G, *x_result, *y_result, *V, *QAX_CENTERS, *QAY_CENTERS;
	double threshold = 1.8, radius = 10.0, delta = 3.0, dt = 0.01, b = 5.0;
	
	// Extract a cropped version of the first frame from the video file
	MAT *image_chopped = get_frame(cell_file, 0, 1, 0);
	printf("Detecting cells in frame 0\n");
	
	// Get gradient matrices in x and y directions
	MAT *grad_x = gradient_x(image_chopped);
	MAT *grad_y = gradient_y(image_chopped);
	
	m_free(image_chopped);
	
	// Get GICOV matrices corresponding to image gradients
	long long GICOV_start_time = get_time();
	MAT *gicov = GICOV(grad_x, grad_y);
	long long GICOV_end_time = get_time();
	
	// Dilate the GICOV matrices
	long long dilate_start_time = get_time();
	MAT *img_dilated = dilate(gicov);
	long long dilate_end_time = get_time();
	
	// Find possible matches for cell centers based on GICOV and record the rows/columns in which they are found
	pair_counter = 0;
	crow = (int *) malloc(gicov->m * gicov->n * sizeof(int));
	ccol = (int *) malloc(gicov->m * gicov->n * sizeof(int));
	for(i = 0; i < gicov->m; i++) {
		for(j = 0; j < gicov->n; j++) {
			if(!double_eq(m_get_val(gicov,i,j), 0.0) && double_eq(m_get_val(img_dilated,i,j), m_get_val(gicov,i,j)))
			{
				crow[pair_counter]=i;
				ccol[pair_counter]=j;
				pair_counter++;
			}
		}
	}

	GICOV_spots = (double *) malloc(sizeof(double) * pair_counter);
	for(i = 0; i < pair_counter; i++)
		GICOV_spots[i] = sqrt(m_get_val(gicov, crow[i], ccol[i]));
	
	G = (double *) calloc(pair_counter, sizeof(double));
	x_result = (double *) calloc(pair_counter, sizeof(double));
	y_result = (double *) calloc(pair_counter, sizeof(double));
	
	x_result_len = 0;
	for (i = 0; i < pair_counter; i++) {
		if ((crow[i] > 29) && (crow[i] < BOTTOM - TOP + 39)) {
			x_result[x_result_len] = ccol[i];
			y_result[x_result_len] = crow[i] - 40;
			G[x_result_len] = GICOV_spots[i];
			x_result_len++;
		}
	}
	
	// Make an array t which holds each "time step" for the possible cells
	t = (double *) malloc(sizeof(double) * 36);
	for (i = 0; i < 36; i++) {
		t[i] = (double)i * 2.0 * PI / 36.0;
	}
	
	// Store cell boundaries (as simple circles) for all cells
	cellx = m_get(x_result_len, 36);
	celly = m_get(x_result_len, 36);
	for(i = 0; i < x_result_len; i++) {
		for(j = 0; j < 36; j++) {
			m_set_val(cellx, i, j, x_result[i] + radius * cos(t[j]));
			m_set_val(celly, i, j, y_result[i] + radius * sin(t[j]));
		}
	}
	
	A = TMatrix(9,4);
	V = (double *) malloc(sizeof(double) * pair_counter);
	QAX_CENTERS = (double * )malloc(sizeof(double) * pair_counter);
	QAY_CENTERS = (double *) malloc(sizeof(double) * pair_counter);
	memset(V, 0, sizeof(double) * pair_counter);
	memset(QAX_CENTERS, 0, sizeof(double) * pair_counter);
	memset(QAY_CENTERS, 0, sizeof(double) * pair_counter);

	// For all possible results, find the ones that are feasibly leukocytes and store their centers
	k_count = 0;
	for (n = 0; n < x_result_len; n++) {
		if ((G[n] < -1 * threshold) || G[n] > threshold) {
			MAT * x, *y;
			VEC * x_row, * y_row;
			x = m_get(1, 36);
			y = m_get(1, 36);

			x_row = v_get(36);
			y_row = v_get(36);

			// Get current values of possible cells from cellx/celly matrices
			x_row = get_row(cellx, n, x_row);
			y_row = get_row(celly, n, y_row);
			uniformseg(x_row, y_row, x, y);

			// Make sure that the possible leukocytes are not too close to the edge of the frame
			if ((m_min(x) > b) && (m_min(y) > b) && (m_max(x) < cell_file->width - b) && (m_max(y) < cell_file->height - b)) {
				MAT * Cx, * Cy, *Cy_temp, * Ix1, * Iy1;
				VEC  *Xs, *Ys, *W, *Nx, *Ny, *X, *Y;
				Cx = m_get(1, 36);
				Cy = m_get(1, 36);
				Cx = mmtr_mlt(A, x, Cx);
				Cy = mmtr_mlt(A, y, Cy);
				
				Cy_temp = m_get(Cy->m, Cy->n);
				
				for (i = 0; i < 9; i++)
					m_set_val(Cy, i, 0, m_get_val(Cy, i, 0) + 40.0);
					
				// Iteratively refine the snake/spline
				for (i = 0; i < Iter; i++) {
					int typeofcell;
					
					if(G[n] > 0.0) typeofcell = 0;
					else typeofcell = 1;
					
					splineenergyform01(Cx, Cy, grad_x, grad_y, ns, delta, 2.0 * dt, typeofcell);
				}
				
				X = getsampling(Cx, ns);
				for (i = 0; i < Cy->m; i++)
					m_set_val(Cy_temp, i, 0, m_get_val(Cy, i, 0) - 40.0);
				Y = getsampling(Cy_temp, ns);
				
				Ix1 = linear_interp2(grad_x, X, Y);
				Iy1 = linear_interp2(grad_x, X, Y);
				Xs = getfdriv(Cx, ns);
				Ys = getfdriv(Cy, ns);
				
				Nx = v_get(Ys->dim);
				for (i = 0; i < Ys->dim; i++)
					v_set_val(Nx, i, v_get_val(Ys, i) / sqrt(v_get_val(Xs, i)*v_get_val(Xs, i) + v_get_val(Ys, i)*v_get_val(Ys, i)));
					
				Ny = v_get(Xs->dim);
				for (i = 0; i < Xs->dim; i++)
					v_set_val(Ny, i, -1.0 * v_get_val(Xs, i) / sqrt(v_get_val(Xs, i)*v_get_val(Xs, i) + v_get_val(Ys, i)*v_get_val(Ys, i)));
					
				W = v_get(Nx->dim);
				for (i = 0; i < Nx->dim; i++)
					v_set_val(W, i, m_get_val(Ix1, 0, i) * v_get_val(Nx, i) + m_get_val(Iy1, 0, i) * v_get_val(Ny, i));
					
				V[n] = mean(W) / std_dev(W);
				
				// Find the cell centers by computing the means of X and Y values for all snaxels of the spline contour
				QAX_CENTERS[k_count] = mean(X);
				QAY_CENTERS[k_count] = mean(Y) + TOP;
				
				k_count++;
				
				// Free memory
				v_free(W);
				v_free(Ny);
				v_free(Nx);
				v_free(Ys);
				v_free(Xs);
				m_free(Iy1);
				m_free(Ix1);
				v_free(Y);
				v_free(X);
				m_free(Cy_temp);
				m_free(Cy);
				m_free(Cx);				
			}

			// Free memory
			v_free(y_row);
			v_free(x_row);
			m_free(y);
			m_free(x);
		}
	}
	
	// Free memory
	free(V);
	free(ccol);
	free(crow);
	free(GICOV_spots);
	free(t);
	free(G);
	free(x_result);
	free(y_result);
	m_free(A);
	m_free(celly);
	m_free(cellx);
	m_free(img_dilated);
	m_free(gicov);
	m_free(grad_y);
	m_free(grad_x);
	
	// Report the total number of cells detected
	printf("Cells detected: %d\n\n", k_count);
	
	// Report the breakdown of the detection runtime
	printf("Detection runtime\n");
	printf("-----------------\n");
	printf("GICOV computation: %.5f seconds\n", ((float) (GICOV_end_time - GICOV_start_time)) / (1000*1000));
	printf("   GICOV dilation: %.5f seconds\n", ((float) (dilate_end_time - dilate_start_time)) / (1000*1000));
	printf("            Total: %.5f seconds\n", ((float) (get_time() - program_start_time)) / (1000*1000));
	
	// Now that the cells have been detected in the first frame,
	//  track the ellipses through subsequent frames
	if (num_frames > 1) printf("\nTracking cells across %d frames\n", num_frames);
	else                printf("\nTracking cells across 1 frame\n");
	long long tracking_start_time = get_time();
	int num_snaxels = 20;
	ellipsetrack(cell_file, QAX_CENTERS, QAY_CENTERS, k_count, radius, num_snaxels, num_frames);
	printf("           Total: %.5f seconds\n", ((float) (get_time() - tracking_start_time)) / (float) (1000*1000*num_frames));	
	
	// Report total program execution time
    printf("\nTotal application run time: %.5f seconds\n", ((float) (get_time() - program_start_time)) / (1000*1000));

	return 0;
}