fastq2array.py 文件源码

def plot(outfn, a, genomeSize, base2chr, _windowSize, dpi=300, ext="svg"):
    """Save contact plot"""

    def format_fn(tick_val, tick_pos):
        """Mark axis ticks with chromosome names"""
        if int(tick_val) in base2chr:
            return base2chr[int(tick_val)]
        else:
            sys.stderr.write("[WARNING] %s not in ticks!\n"%tick_val)
            return ''

    # invert base2chr
    base2chr = {genomeSize-b: c for b, c in base2chr.iteritems()}
    # start figure
    fig = plt.figure()
    ax = fig.add_subplot(111)
    ax.set_title("Contact intensity plot [%sk]"%(_windowSize/1000,))
    # label Y axis with chromosome names
    if len(base2chr)<50:
        ax.yaxis.set_major_formatter(FuncFormatter(format_fn))
        ax.yaxis.set_major_locator(MaxNLocator(integer=True))
        plt.yticks(base2chr.keys())
        ax.set_ylabel("Chromosomes")
    else:
        ax.set_ylabel("Genome position")
    # label axes
    ax.set_xlabel("Genome position")        
    plt.imshow(a+1, cmap=cm.hot, norm=LogNorm(), extent=(0, genomeSize, 0, genomeSize))# 
    plt.colorbar()
    # save
    fig.savefig("%s.%s"%(outfn,ext), dpi=dpi, papertype="a4")