Generative models enable the translation from a source image domain where readily trained models are available to a target domain unseen during training. While Cycle Generative Adversarial Networks (GANs) are well established, the associated cycle consistency constrain relies on that an invertible mapping exists between the two domains. This is, however, not the case for the translation between images stained with chromogenic monoplex and duplex immunohistochemistry (IHC) assays. Focusing on the translation from the latter to the first, we propose - through the introduction of a novel training design, an alternative constrain leveraging a set of immunofluorescence (IF) images as an auxiliary unpaired image domain. Quantitative and qualitative results on a downstream segmentation task show the benefit of the proposed method in comparison to baseline approaches.
The creation of in-silico datasets can expand the utility of existing annotations to new domains with different staining patterns in computational pathology. As such, it has the potential to significantly lower the cost associated with building large and pixel precise datasets needed to train supervised deep learning models. We propose a novel approach for the generation of in-silico immunohistochemistry (IHC) images by disentangling morphology specific IHC stains into separate image channels in immunofluorescence (IF) images. The proposed approach qualitatively and quantitatively outperforms baseline methods as proven by training nucleus segmentation models on the created in-silico datasets.