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USRE40674E1 - Analog circuit for an autofocus microscope system - Google Patents

Analog circuit for an autofocus microscope system
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USRE40674E1
USRE40674E1US10/000,943US94301AUSRE40674EUS RE40674 E1USRE40674 E1US RE40674E1US 94301 AUS94301 AUS 94301AUS RE40674 EUSRE40674 EUS RE40674E
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microscope
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Jeffrey H. Price
Miguel Bravo-Zanoguera
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Q3DM LLC
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Abstract

An analog circuit for an autofocus microscope system measures a degree of focus of an object directly from the video signal of a microscope CCD camera. The circuit then returns an index to a host computer for the purpose of adjusting the position of the microscope's objective lens to bring the object in focus. Best focus is found by comparing indices at several different vertical positions. The criterion adopted for determining the degree of focus is derived from the energy distribution of the video signal spectrum. The high frequency energy of the video spectrum is a maximum at best focus and as the optics defocus, the distribution shifts to lower frequencies. Low cost, real time autofocus is achieved with the analog circuitry of this invention, replacing more expensive dedicated, real time image processing hardware.

Description

BACKGROUND OF THE INVENTION
The invention is in the field of microscopy in which focus of an image, observed by way of a microscope, is automatically adjusted. Such automatic adjustment of microscope focus is termed “autofocus”. The invention is practiced in an autofocus system. More particularly, the invention concerns the incorporation of an analog circuit that accounts for the effect of a transfer function attributable to the microscope optics of the autofocus system, eliminates scanning artifacts that impair the autofocus function, and corrects for illumination instability.
Autofocus is essential in automated microscopy to overcome the problems of mechanical instability, the irregularity of glass slides and coverslips, the movement of live specimens and the effects of thermal expansion. Autofocus can overcome these limitations and allow accurate and reproducible measurements in fully automated quantitative microscopy. Many experiments will benefit from autofocus and examples for which it is indispensable include:
    • (a) scanning large areas at high resolution where depth of field is limited (e.g. cervical cancer screening, with 10,000 microscope fields per slide).
    • (b) time-lapse experiments (e.g. hours to days).
    • (c) time-lapse scanning cytometry combining (a) and (b), where autofocus speed becomes a fundamental determinant of temporal resolution.
      Whatever the source of instability, autofocus will compensate if the positional variations have longer time constants than the autofocus correction.
An autofocus system typically includes an automated microscope including magnifying optics and an adjustable stage on which a microscope slide is mounted for magnified observation of a specimen on the slide. Motors coupled to the stage provide horizontal adjustment of the location of the stage. Means are provided for vertical (Z-axis) adjustment between the magnifying optics and stage. These may include an arrangement for adjusting the Z-axis position of an objective lens, or by Z-axis adjustment of the stage. A camera receives a magnified image via the magnifying optics and provides an electronic signal representing the magnified image to autofocus electronics. The autofocus electronics process the signal according to a function that indicates the degree of focus, providing an adjustment (or error) signal to the vertical adjustment means. In response, the vertical adjustment means adjusts the vertical position of the objective lens or the stage, changing the focus of the magnified image. Other circuit may be included in an autofocus system for automatic translation (scanning) of a specimen on the slide.
Several methods have been tested for autofocus, including resolution, contrast and entropy. It has recently been shown that a measurement of optical resolution performs autofocus robustly and accurately. Price, J. H. and Gough, D. G., “Comparison of Phase-Contrast and Fluorescence Digital Autofocus for Scanning Microscopy,” Cytometry 16, pp. 283-297, 1994. This experimental evidence reinforces the following logical definition: the highest resolution occurs at best focus. Details blur as an image is defocused and resolution is lost. Resolution can be measured by analyzing the Fourier frequency spectrum with filters that isolate the high frequencies. The sum of the squares of the high frequencies (signal power) can then be used as a measured of resolution. In spectral terms, this can be a highpass or bandpass filter. A typical filter is implementation of the first derivative of the image intensity. Another is the laplacian filter, which is a measure of the second derivative of the image intensity. The laplacian filter has more predominant highpass characteristics, measuring resolution at a smaller scale. Squaring magnifies the differences between function values.
To compare different criteria, an autofocus system typically computes focus functions as a function of the Z-axis position. A value of the focus function is calculated from an image acquired at each Z-axis position. According to Price et al., a typical equation for the focus function using a digital filter consists of convolving the image ixywith a one dimensional highpass filter, obtaining the sum of squares and normalizing to reduce the effect of unstable illumination. Such a relationship is given in equation (1).
f(z)=ΣΣ([−1 2−1]*ixy)2/[(1/XY of pixels)(ΣΣixy)]2  (1)
where z=vertical position and ixyis the intensity at position (x,y).
Analog focus circuits have been reported in Ali Kujoory, M., Mayall, B. H. and Mendelsohn, M. L., “Focus-Assist Device for a Flying-Spot Microscope,” IEEE Transactions on Biomedical Engineering, 20(2), pp. 126-32, 1973, and in Johnson, E. T. and Goforth, L. J., “Metaphase Spread Detection and Focus Using Closed Circuit Television”, Journal of Histochemistry and Cytochemistry, 22(7), pp. 536-587, 1974. McKeogh, L., Sharpe, J., and Johnson, K., in “A Low-Cost Automatic Translation and Autofocusing System for a Microscope”, Meas. Sci. Technol., 6, pp. 583-587, 1995, describe an analog circuit for autofocus in microscopy. These designs, however do not take into account the effect of the autofocus system transfer function in the choice of the high frequency filter. Additional important features not considered in these previous implementations include the filter end effects between horizontal lines in the video signal and normalization for correction of illumination instability. Further, in low information content images, background intensity changes can dominate via filter distortion at the ends of horizontal lines.
SUMMARY OF THE INVENTION
The goal of this invention is to implement fast, accurate autofocus at a low cost for use in, for example, scanning microscopy, of fluorescent stained biologic specimens.
The invention is practiced in an autofocus system having a microscope, a source of video signal representing a magnified image produced by the microscope, and an automatic microscope focus control that focuses the microscope in response to a focus index signal. The invention is embodied in this context by an analog circuit that produces the focus index signal. The circuit includes a filter that provides a filtered signal representing predetermined frequencies in the video signal. A transient remover is connected to the filter for removing scanning artifacts from the filtered signal. A squaring circuit connected to the transient remover squares magnitudes of predetermined frequency components of the filtered signal. An integrator connected to the squaring circuit produces a focus index signal representing a degree of focus of the microscope by integrating the squared magnitudes of the frequency components of the filtered signal.
Preferably, the circuit further includes an integrator that produces an average illumination signal in response to the video signal. Both the focus index signal and the average illumination signal are combined by a processor in the focus control of the autofocus system to produce a focus position signal representing a focus position of the microscope. The focus control utilizes the focus position signal to adjust the microscope to the focus position.
Assuming a video signal produced by interlaced scanning, the transient remover may also create a window imposed on the video signal to define an area of the magnified image were a focus index signal will be produced.
An objective of the invention is therefore to provide an analog circuit for an autofocus system that produces a focus index signal representing a degree of focus.
A further objective is a provision by such a circuit of an average illumination signal that can be combined with a focus index signal by a processor to produce a focus position signal.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a block diagram of a complete autofocus microscope system;
FIG. 2 is a block diagram of an analog circuit for an autofocus microscope system;
FIGS. 3a and 3b are plots of waveforms that illustrate operation of the analog circuit ofFIG. 2;
FIG. 4, comprising ofFIGS. 4A,4B,4C and4D is an electronic circuit schematic diagram illustrating the best mode for implementing the analog circuit ofFIG. 2;
FIG. 5 is graph illustrating digital and analog focus function curves illustrating experimental results with the operation of an autofocus microscope system with the analog circuit ofFIGS. 2 and 4; and
FIG. 6 is a graph showing analog focus function curves at different zooms for a thick cell monolayer by the autofocus microscope system of FIG.1.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
Refereeing now to the figures where like reference numerals indicate identical elements, inFIG. 1 there is illustrated anautofocus system10 including amicroscope12 that includes anobjective lens14, and amicroscope stage16 on which a slide may be mounted. Thestage16 is translatable in the X and Y directions so that a succession of areas on a microscope slide carried on the stage can be scanned according to known methods. One such area is indicated byreference numeral18. The microscope includes means20 for illumination of fluorescent stained biologic specimens and means22 for phase contrast or other transmitted microscopy illumination. An image of thearea18 is magnified by magnifying optics of themicroscope12 that include theobjective lens14 and azoom lens23. Each magnified image is acquired by acamera30 that produces, by interlaced scanning, a video signal representing a magnified image, and including various synchronization components that are necessary for interlaced scanning. The video signal is provided onsignal path32 to a programmed, general purposedigital computer34 that includes, among other functions, animage processor38 and afocus signal processor39.
The video signal is also provided to ananalog autofocus circuit36 that embodies the invention. Theanalog autofocus circuit36 produces a focus index signal, an average illumination signal, and a trigger signal, that are produced on asignal paths40,42 and44, respectively to thefocus processor39 of thecomputer34.
Thefocus processor39 of thecomputer34 constitutes an automatic microscope focus control that calculates a focus function signal in response to the focus index, average illumination, and trigger signals. A focus function signal is produced at each of a plurality of focus positions at themicroscope12. These are combined by thefocus processor39 to produce a focus position signal representing a focus position of themicroscope12. The focus position signal is provided onsignal path50 and used to control known means that adjust the position of theobjective lens14, thereby focusing themicroscope12. Other signals are provided onsignal path52 for adjusting the X and Y positions of thestage16.
An autofocus system not including theanalog autofocus circuit36 is set forth atcolumn 12, line 28-column 14,line 36 of U.S. Pat. No. 5,548,661, which is incorporated in its entirety by this reference.
Hardware and Experimental Methods
Theautofocus system10 was set up for phase contrast and brightfield illumination for analog operation according to the invention. Cells were imaged in a Nikon Optiphot microscope through aCF Fluor DL 40+C, 0.85 NA objective lens with Ph3 bright phase contrast. The images were further magnified through a Nikon CCTV 0.9-2.25 zoom lens onto a Dage VE-1000 CCD RS-170 camera, with a frequency response of 7 MHz. Themicroscope stage16 was moved in the X, Y plane under control of thecomputer34 by stepper motors for fluorescent image cytometry. Control of themicroscope stage16 was by way of a microstepping driver and an AT ISA-bus compatible computer board.
Focus was changed by changing the position of theobjective lens14 with a piezoelectric objective positioner (PIFOC) and an E-S810.10 closed loop controller (Polytec PI, Costa Mesa, Calif.). For movements of ≦1 μm, the position of theobjective lens14 is stable in 10 ms. The position of the PIFOC was controlled by output from a digital-to-analog (D/A) converter in a Keithley Metrabyte (Taunton, Mass.) DAS 1600 data acquisition board incorporated in thecomputer34. The 12-bit D/A converter divides the 100 μm range of the PIFOC into 4,096 steps of 24 nm each.
Theimage processor38, using an RS-170 video input board, (the VLSI-150 by Imaging Technology Inc), captured the magnified image in the form of the video signal and applied an anti-aliasing filter of −3 dB and 4.2 MHz and −12 dB attenuation at 8 MHz. These values were used as a reference to design the filters of the analog circuit of this invention and make it comparable in response to the digital version.
Analog Circuit Implementation
The invention provides ananalog autofocus circuit36 that measures the degree of focus directly from the video signal of thecamera30 and solves previous design limitations. The block diagram of FIG.2 and circuit diagram ofFIG. 4 illustrate the functional components of this novel circuit. The criterion adopted for determining a degree of defocus was the relative energy contained in the magnified image as a function of spatial frequency. Under defocus, adjacent elements of the magnified image were blurred or averaged together, causing loss of higher spatial frequencies. By measuring the relative energy in these frequencies as a function of focal position, a criterion for determining the optimal focus position was established, since the energy changes monotomically and is maximum at focus. These assumptions hold for phase contrast only when high frequencies are utilized for the focus criteria. Monotonicity is often violated under these conditions when low frequencies are involved. Price et al., op cit.
Theanalog circuit36 implements the focus function in the integral of the squared values of the video signal, as a measure of the energy in the image. The video signal is filtered prior to squaring to accentuate the high frequencies that are most dependent on focus. Equation (2) represents the processing achieved by theanalog circuit36 and thecomputer34. In terms of circuit components, thefilter52 selects the range of frequencies from the video image signal and, after squaring and integrating, theanalog circuit36 produces a focus index value ∫∫(dIx,y/dx)2dxdy that is returned to thecomputer34 as the magnitude of the focus index signal along with an average illumination value (Ix,y) (the magnitude of the average illumination signal). After A/D conversion, thecomputer34, using thefocus signal processor39, squares the average illumination value and performs the following division to produce a focus function F(z):
F(z)=˜˜(dIx,y/dx)2dxdy/(˜˜Ix,ydxdy)2  (2)
The shape of the focus function is determined by the focus criterion, the microscope and the camera transfer functions, and the imaged object. The properties of a useful focus function are: 1) unimodality, only one maximum; 2) accuracy, the maximum occurs at the in focus position; 3) reproducibility, the sharpness of the focus function curve; 4) implementation, fast calculation of the focus value. Price et al., op. cit., and Groen, F. C. A., Young, I. T. and the Ligthart, G., “a Comparison of Different Focus Functions for Use in Autofocus Algorithms,”Cytometry 6, pp. 81-91, 1985. Analog circuits have a substantial advantage over digital circuits in implementation if they can match digital circuit performance for the first three properties. This is because analog components operating at conventional video frequencies are relatively ubiquitous and inexpensive.
Theanalog circuit36 measures focus directly from the video signal. The output of thecamera30 is in conventional scanned video format, comparing two interlaced fields. Theanalog circuit36 can be divided into an analog section and a digital/timing section. The analog portion can be further separated into a focus index part and an average illumination part. Three signals are provided to thecomputer34 by the analog circuit36: a focus index signal, an average illumination signal and a trigger pulse.
Referring now toFIGS. 2 and 4, the video signal representing a magnified image of thearea18 is provided to aconventional sync stripper50 that eliminates the horizontal and vertical pulses from the video signal. The output of thesync stripper50 is fed to the input of abandpass filter52 having a transfer function H(ω). The filter has a frequency response that passes the high frequency components of the video signal for the reasons given above. Thefilter52 produces a filtered signal representing the predetermined high frequencies in the image signal. The filtered signal is provided on an output of thefilter52 that is connected to the input of atransient removal element56. Thetransient removal element56 is gated by synchronization signals extracted from the video signal. In the preferred embodiment, the gating eliminates scanning artifacts produced at the beginning and ending of each of the scan lines of the image signal. In effect, thetransient removal element56 may also be regarded as a window generator which, for each scan line in the video signal, enables a window that is shorter than the scan line, with the respective ends of the scan line extending beyond the ends of the window. Provision of the vertical sync pulse enables thetransient removal element56 to produce a two-dimensional window that may moved over each of the two interlaced fields forming a frame of video in the typical scanned format. Thetransient removal element56 provides the filtered signal, with scanning artifacts removed therefrom, on an output that is connected to the input of squaringcircuit58. The squaring circuit squares the magnitude of the predetermined frequency components in the filtered signal, providing the squared magnitudes on an output that is connected to the input of anintegrator60. Theintegrator60 integrates the squared magnitudes of the frequency components of the filtered signal, producing a focus index signal in analog form that is provided to a sample and holdcircuit62. The sample and holdcircuit62 is gated to hold a voltage magnitude of the integrated signal produced by theintregrater60. The voltage magnitude of the integrated signal (the focus index signal) represents a degree of focus of themicroscope12. The focus index signal is provided on thesignal path40 to thecomputer34. Theelements52,56,58,60, and62 therefore form a focus index part of the analog portion of theanalog circuit36. An average illumination part of theanalog circuit36 is formed by anintegrator68 that integrates the video signal, stripped of its sync signals by thesync stripper50. The integration of the video signal by theintegrator68 over, for example, a line of video, represents average illumination over the line. The magnitude of theintegrator68 is sampled and held by sample and holdcircuit70 whose output forms the average illumination signal provided onsignal path42.
The digital portion of theanalog circuit36 consists of acontrol timing circuit66 the receives the image signal intact, including all of its scanning artifacts, such as vertical and horizontal sync portions. Thecontrol timing circuit66 generates reset and hold signals that sequentially synchronize the operations of theintegrators60 and68 in the sample and holdcircuits62 and70, respectively. In addition, thecontrol timing circuit66 produces the trigger signal on the signal line46.
Thecontrol timing circuit66 further produces the sync signals necessary to form the window implemented by thetransient removal element56.
Digital Section
With reference toFIGS. 2 and 4, the synchronization pulses of the video signal are detected in thecontrol timing circuit66 by a sync separator80 (LM1881, National Semiconductor, Arlington, Tex.) which extracts the horizontal and vertical pulses. This timing information is used to create a window that represents an area of the image where the focus function will be implemented. At the very least, the window allows removal of the discontinuities generated by thefilter52 at the ends of horizontal lines. This portion of theanalog circuit36 can be used as a mask generator to select an arbitrary rectangular portion of a video field for processing; any window size can be defined vertically and horizontally by changing the time constants of the two monostable multivibrators. A first portion of the window is established byflip flops82a and82b; the second portion by flip-flops83a and83b. This type of analog masking has been used for video-dimension analyzers. Yin, F. C. P., Tompkins, W. R., Peterson, K. L. and Intaglietta M., “A Video-Dimension Analyzer,” IEEE Transactions on Biomedical Engineering, 19(5), pp. 376-81, 1972. The window information is used by agated amplifier84 in thetransient removal element56. After each window, or video field, a trigger pulse is generated. Thecontrol timing circuit66 also produces a sequence of 60 Hz trigger signals that gate thecomputer34 for A/D conversion of the corresponding analog values for each field.
Analog Section
Thefilter52 is implemented with wide-bandwidth monolithic amplifiers90-96 having high slew rates and internal unity-gain frequency compensation for high speed and stability. Such high frequency, high-speed amplifiers are more prone to oscillations than low frequency devices. However, this instability was eliminated by reducing the stray capacitance at amplifier inputs and outputs. Power supply bypassing was also used for stability enhancement, and small capacitors were added parallel to the feedback resistors to compensate for unavoidable stray capacitance in the filters.
FIG. 3a shows the plot of ahorizontal video line100 and selected subsequent analog processed outputs. Thesync stripper50 removes the sync portion of the composite video signal perwaveform102. The reference level is at ground and since the sync tip is negative the output will have the sync removed and place the blanking level at ground. After the video signal input is stripped of its synchronizing pulses, the signal is fed to both thefilter52 in the focus index section and theillumination integrator68.
Each of the operational amplifiers90-96 of the filter (LT1220, Linear Technology Corporation, Milpitas, Calif.) is used in a two-pole active Butterworth filter configuration, with the four operational amplifiers arranged in a 4thorder lowpass sections52a and a 4thorder highpass section52b. A frequency response from 2 to 4 MHz was selected, for matching the digital filter response, which represents the transfer function of the optics in themicroscope12. A bandpass gain of 2.56 was used to compensate for signal attenuation. Due to the wide bandwidth and unity compensation of the components, good performance was obtained without further custom design. With the correct choice of the components, cutoff frequency is independent of amplifier bandwidth, and is determined only by the respective R-C networks in the low-pass section52a and the high-pass section52b. Manifestly, these networks may include manually-adjustable elements.Waveform104 demonstrates the filter output.
The windowed, filtered signal is offset, amplified and squared, as shown inwaveforms106 and108. The filtered, squared signal is then integrated over one video field by theintegrator60. Theintegrator60 includes reset, integrate the filtered signal for focus index calculation, and, over thediode114, hold intermediate focus while there is no significant output from thefilter52. Previous analog autofocus circuit designs, lacking the hold control, exhibited focus index output decay between image features. This is illustrated clearly bywaveform109 inFIG. 3a, where, over the portion of the squaredwaveform108 marked “dead space”, the magnitude of the integrated signal produced by theintregrator60 does not decay. Using theintegrator60 withdiode114 instead of the conventional integrator ensures that the focus index more ideally matches the true mathematical integral for each video field. The output of theintegrator68 is similarly controlled bycapacitor116 anddiode118.
The average illumination section takes the sync stripped video signal and measures the average illumination by integrating the signal over one field. A sample and hold circuit is used to maintain the final analog values for the A/D board. The final output from this integration, and the focus index, are then converted by the analog-digital board in thecomputer34. The trigger signal is sent to the computer at the end of each field to start a new conversion. Focus index, average illumination and trigger, with their respective grounds, are conventionally connected to thecomputer34 orsignal paths40,42 and46, respectively.
Windowing in theanalog circuit36 is shown inFIG. 3b, and can be understood with reference toFIGS. 2 and 4. For the scan line dimension, ahorizontal window pulse120 is created for any line of video by the flip-flops82a-82b in response to horizontal line blanking. Avertical window pulse124 is produced by the flip-flops83a-83b in response to vertical blanking. The transistor-diode circuit126 responds to thepulses120 and124 as an AND gate, transmitting the filtered signal from thefilter52 to the squaringcircuit58 when both pulses are high. Manifestly, counting or timing may be employed with the flip-flops in thecontrol timing circuit66 to selectively adjust the dimensions of a window.
Focusing Software, Autofocus Algorithm
In thefocus processor39, an interrupt service routine (ISR) was implemented to acquire the analog value of the focus index and average illumination signals, based on the trigger signal supplied by theanalog circuit36. This routine also controlled focus position, acquisition of the analog values from the autofocus circuit and calculation of the normalized degree of focus. Programs were written in C and assembler languages. The C routines were complied with Metaware High C (Santa Cruz, Calif.). A Phar Lap (Cambridge, Mass.) assember was used for the interrupt service routines.
At the end of each field a trigger pulse starts the ISR, which transfers the analog values of the focus index and average illumination signals to arrays accessible to C routines for calculating and setting best focus.
In order to determine a best focus, thecomputer34 executes a focus sequence in which the Z-axis position of theobjective lens14 is sequenced through a plurality of focus positions (zi). At each focus position the magnitude of the focus index and average illumination signals are taken and a focus function value (F(zi) is calculated according to equation (2). Focus function values are stored at130,FIG. 1, by thecomputer34.
After each focus sequence, with focus indices stored by thecomputer34 for a number of positions, a power-weighted average is used to find best focus. Unusually shaped focus curves containing multiple extrema may be produced by discrete vertical distributions of cellular components. For these reasons, the weighted averageWa=z(fz)n(fz)n(3)
is used, where Wais the power-weighed average position, z is the vertical (Z-axis) position, Fxis the result of the focus function (equation (2)) calculated from an image acquired at one z position, and n is the power of the weighting. The power accentuates the peak values and the average reduces the effect of the 3D nature of the specimen.
Experimental Results
Contrast in a microscope image is not an inherent property of a specimen. Rather it is a product of (1) the interaction of the illuminating light waves and specimen structure and (2) the MTF and contrast generation mode of the microscope. Point (1) depicts both in specimen structure and on the condition of the illuminating light wave; point (2) depends both on the condition of the illumination and how the waves leaving the specimen are treated. Inoué, S., “Video Microscopy”, Plenum Press, New York, 1986.
Phase contrast microscopy was used as the imaging technique for autofocus in these experiments. In phase contrast, phase changes introduced by the transparent cells are transformed into changes in intensity. Born, M. and Wolf, E., “Principles of Optics”, Pergamon Press, 1989. This creates contrast in the image that is useful for performing autofocus. Phase contrast also performs an optical highpass filter. Inoué, S., “Video Microscopy”, Plenum Press, New York, 1986. Experimentally, phase contrast has also been shown to be more prone to exhibit side peaks in the focus function curve. Price, J. H. et al., op cit. Thus, it is important to carefully select the high frequencies to ensure unimodality.
InFIG. 5 the plot of a phase-contrast experiment of a cell monolayer at different Z-axis positions is shown. Similar focus function curves are obtained by the analog and the digital versions, peak widths and sharpness of the functions are primarily unimodal. The curves exhibit damped side peaks outside the main lobe. This behavior is exacerbated by undersampling at unit zoom. Increasing the magnification results in he Nyquist sampling and this behavior is eliminated. The low cutoff of the filter captures mid-range frequencies for which a monotonic behavior cannot be assumed. The tendency toward side peaks is reduced with the increased frequency response of the focus index system transfer function, which includes the filter, CCD camera, and optical transfer function.
FIG. 6 shows a plot of the analog focus index using a thick cell monolayer. The 3-D structure of the specimens creates differences of best focus and accounts for the broadening of the focus function. The increased specimen depth also seems to enhance the side peaks. Thus, the shape of the focus curve depends both on the specimen and the system transfer function. The sampling period for a particular experimental condition was calibrated using images of a micrometer slide with a 10 μm spacing. At a zoom of 1× (using the 40×objective) the period was 33 nm. The resolving power is given by the Rayleigh criterion, d=1.22λ/(NAobj+NAcond). With a 500 nm illumination, a 0.52 NAcondand 0.85 NAobj, a resolution of 445 nm is obtained. The required Nyquist sampling is then 225.5 nm. A magnification of (303/222.5)=1.36× is thus required for Nyquist sampling. For a variety of practical reasons, one must, in fact, oversample further. Inoué, S., op. cit.
The principal advantage of this carefully designed analog circuit is low cost with no performance sacrifice. The digital processing for real time autofocus demands the use of a real time image processor with pipeline architecture which can be an order of magnitude more expensive. In addition, increasing the complexity of the digital filter involves adding coefficients, which can further increase cost or reduce speed. On the other hand, digital autofocus makes reprogramming a simple task, and for real time operation, the digital image processing resources can be used for simple one-dimensional filters as discrete approximations of the derivative filters (e.g. the {1, −1} and {−1, 2, −1} highpass filters and the {1, 0, −1} bandpass filter). Given the cost of the digital image processing, however, replacement of the digital implementation with an inexpensive analog circuit of equal performance that frees this important resuce for other tasks may be the most important consideration.
One drawback with analog circuits in general (at least with respect to their digital equivalents) is limited dynamic range. The digital dynamic range is proportional to the square root of the product of the pixels and gray levels. Analog processing is limited to the number of bits of an A/D converter. Of course, the limited analog dynamic range could be overcome by addition of an automatic gain control circuit. On the other hand, analog implementation permits an arbitrary upper cutoff frequency (up to the limit of the camera), whereas in the digital version this upper limit is set by the image processor. This simplifies matching the focus cutoff frequency in thefilter52 to the microscope optical transfer function to generate a sharper filter function curve for improved autofocus reproducibility. Assuming, a CCD camera capable of 768 pixels/line,image processor38 digitized only 512 pixels/line. With theanalog circuit36, plug-in headers may be used for thefilter52 to simplify matching of the filter function with each video camera and optical transfer function combination. Theanalog circuit filter52 is much easier and less expensive to change than the resolution of theimage processor38.
While the above detailed description has shown, described and pointed out the fundamental novel features of the invention as applied to various embodiments, it will be understood that various omissions and substitutions and changes in the form and details of the device illustrated may be made by those skilled in the art, without departing from the spirit and scope of the claimed invention.

Claims (28)

1. In an autofocus system having a microscope, a source of an image signal representing a magnified image produced by the microscope, and an automatic microscope focus control that focuses the microscope in response to a focus index signal, a circuit for producing the focus index signal, comprising:
a filter for providing a filtered signal representing predetermined frequencies in the image signal;
a transient remover connected to the filter for removing scanning artifacts from the filtered signal;
a squaring circuit connected to the transient remover for squaring magnitudes of frequency components of the filtered signal; and
an index integrator connected to the squaring circuit for producing a focus index signal representing focus of the microscope by integrating squared magnitudes of the frequency components of the filtered signal.
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US5995143A (en)1999-11-30
CA2283088A1 (en)1998-08-13
EP1021741A1 (en)2000-07-26
ATE223070T1 (en)2002-09-15
CN1246929A (en)2000-03-08
BR9807671A (en)2000-02-15
EP1021741B1 (en)2002-08-28
WO1998035256A1 (en)1998-08-13
DE69807512D1 (en)2002-10-02

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