diff --git a/jcvi/graphics/landscape.py b/jcvi/graphics/landscape.py index 1d1d3c42..f4470786 100644 --- a/jcvi/graphics/landscape.py +++ b/jcvi/graphics/landscape.py @@ -572,7 +572,10 @@ def check_window_options(opts): return window, shift, subtract, merge -def get_beds(s, binned=False): +def get_beds(s: List[str], binned: bool = False) -> List[str]: + """ + Get the bed files for each feature, and return them as a list. + """ return [x + ".bed" for x in s] if not binned else [x for x in s] @@ -989,7 +992,7 @@ def get_binfiles( mode: str = "span", subtract: Optional[int] = None, binned: bool = False, - merge: bool=True, + merge: bool = True, ): """ Get binfiles from input files. If not binned, then bin them first. @@ -1052,39 +1055,21 @@ def stackplot( ax.set_axis_off() -def stack(args): +def draw_stack( + fig, + root, + stacks: List[str], + fastafile: str, + window: int, + shift: int, + top: int, + merge: bool, + subtract: Optional[int] = None, + switch: Optional[DictFile] = None, +): """ - %prog stack fastafile - - Create landscape plots that show the amounts of genic sequences, and repetitive - sequences along the chromosomes. + Draw stack plot. """ - p = OptionParser(stack.__doc__) - p.add_option("--top", default=10, type="int", help="Draw the first N chromosomes") - p.add_option( - "--stacks", - default="Exons,Introns,DNA_transposons,Retrotransposons", - help="Features to plot in stackplot", - ) - p.add_option("--switch", help="Change chr names based on two-column file") - add_window_options(p) - opts, args, iopts = p.set_image_options(args, figsize="8x8") - - if len(args) != 1: - sys.exit(not p.print_help()) - - (fastafile,) = args - top = opts.top - window, shift, subtract, merge = check_window_options(opts) - switch = opts.switch - if switch: - switch = DictFile(opts.switch) - - stacks = opts.stacks.split(",") - - fig = plt.figure(1, (iopts.w, iopts.h)) - root = fig.add_axes((0, 0, 1, 1)) - bedfiles = get_beds(stacks) binfiles = get_binfiles(bedfiles, fastafile, shift, subtract=subtract, merge=merge) @@ -1094,8 +1079,6 @@ def stack(args): margin = 0.08 inner = 0.02 # y distance between tracks - pf = fastafile.rsplit(".", 1)[0] - # Gauge ratio = draw_gauge(root, margin, maxl) @@ -1140,10 +1123,47 @@ def stack(args): root.text(xx, yy, b, size=13) xx += len(b) * 0.012 + inner - root.set_xlim(0, 1) - root.set_ylim(0, 1) - root.set_axis_off() + normalize_axes(root) + +def stack(args): + """ + %prog stack fastafile + + Create landscape plots that show the amounts of genic sequences, and repetitive + sequences along the chromosomes. + """ + p = OptionParser(stack.__doc__) + p.add_option("--top", default=10, type="int", help="Draw the first N chromosomes") + p.add_option( + "--stacks", + default="Exons,Introns,DNA_transposons,Retrotransposons", + help="Features to plot in stackplot", + ) + p.add_option("--switch", help="Change chr names based on two-column file") + add_window_options(p) + opts, args, iopts = p.set_image_options(args, figsize="8x8") + + if len(args) != 1: + sys.exit(not p.print_help()) + + (fastafile,) = args + top = opts.top + window, shift, subtract, merge = check_window_options(opts) + switch = opts.switch + if switch: + switch = DictFile(opts.switch) + + stacks = opts.stacks.split(",") + + fig = plt.figure(1, (iopts.w, iopts.h)) + root = fig.add_axes((0, 0, 1, 1)) + + draw_stack( + fig, root, stacks, fastafile, window, shift, top, merge, subtract, switch + ) + + pf = fastafile.rsplit(".", 1)[0] image_name = pf + "." + iopts.format savefig(image_name, dpi=iopts.dpi, iopts=iopts) diff --git a/jcvi/projects/jcvi.py b/jcvi/projects/jcvi.py index 54d19b45..3fc52b4d 100644 --- a/jcvi/projects/jcvi.py +++ b/jcvi/projects/jcvi.py @@ -105,10 +105,10 @@ def landscape(args): p = OptionParser(landscape.__doc__) _, args, iopts = p.set_image_options(args, figsize="10x7") - if len(args) != 3: + if len(args) != 4: sys.exit(not p.print_help()) - bedfile, sizesfile, pngfile = args + bedfile, sizesfile, fasta, ch = args fig = plt.figure(1, (iopts.w, iopts.h)) root = fig.add_axes((0, 0, 1, 1)) @@ -134,20 +134,7 @@ def landscape(args): # Panel B logger.info("Plotting landscape of genomic features across the genome") - M = plt.imread(pngfile) - width, height = M.shape[1], M.shape[0] - # Split the image into left and right parts - mid = width // 2 - 10 - left_cut = right_cut = 900 - logger.info("Image size: %dx%d", width, height) - logger.info("Splitting image at %d", mid) - - LM, RM = M[:left_cut, :mid], M[:right_cut, mid:] - logger.info("Left image size: %dx%d", LM.shape[1], LM.shape[0]) - logger.info("Right image size: %dx%d", RM.shape[1], RM.shape[0]) - - ax2_root.imshow(LM, extent=(0.4, 1, 0.5, 1), aspect="auto") - ax3_root.imshow(RM, extent=(0.4, 1, 0, 0.5), aspect="auto") + ax2_root.set_axis_off() ax3_root.set_axis_off()