Abstract

Low illumination environment in Fluorescence microscopy, create arbitrary variations in the photon emission and detection process that manifest as Poisson noise in the captured images. Therefore study the effect of Standard denoising algorithms wherein the noise is either transformed to Gaussian or the denoising is done on the Poisson noise itself. In the first strategy the noise is Gaussianized by applying the Anscombe root transformation to the data, to produce a signal in which the noise can be treated as additive Gaussian and then the consequential image is denoised using conservative denoising algorithms for additive white Gaussian noise such as BLS_GSM and OWT_SURELET and finally the inverse transformation is done on the denoised image. The choice of the proper inverse transformation is vital for fluorescence images in order to reduce the bias error which arises when the nonlinear forward transformation is applied. The Latter strategy considers PURELET technique where the denoising process is a Linear Expansion of Thresholds (LET) that optimize results by depending on a purely data-adaptive unbiased estimate of the Mean-Squared Error (MSE), derived in a non-Bayesian framework (PURE: Poisson-Gaussian unbiased risk estimate). Experimental results are compared with exisitng work on how the ISNR changes with the change in algorithms for fluorescence images.

Highlights

  • Fluorescence microscopy is a popular live imaging practice, used to image biological specimens

  • In this study study the result of the PURELET algorithm whereas PURE algorithm unbiased results are estimated by using Haar wavelet domain, of the meansquared error among the original image and the estimated image (Portilla et al, 2003)

  • Gaussian based denoising approach constitutes of the same three-step denoising forward Anscombe transformation (4) procedure to a noisy image after which denoising of the transformed image with OWT_SURELET (Thierry and Florian, 2007) BLS_GSM (Portilla et al, 2003) and apply an inverse transformation in order to get the final estimate

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Summary

Introduction

Fluorescence microscopy is a popular live imaging practice, used to image biological specimens. This technique has rigid constraints for parameters like acquisition-time and photo toxicity. Low illumination conditions generate arbitrary variations in the photon emission and detection process that manifest as Poisson noise in the captured images (Sampath and Arun, 2012). In this study main aim of the work is to establish the impact of various standards denoising strategies on fluorescence images (Sampath and Arun, 2013). Photon and camera readout noises in general degrade fluorescence images. Consider strategies which work on the Poisson noise or Gaussianize the Poisson process and denoise the Gaussianized image (Luisier et al, 2010)

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