arXiv subjects

Smita Krishnaswamy

Publications and source records attributed to Smita Krishnaswamy.

77 records · Page 5Linked to original sources

arXiv2019

TraVeLGAN: Image-to-image Translation by Transformation Vector Learning

Interest in image-to-image translation has grown substantially in recent years with the success of unsupervised models based on the cycle-consistency assumption. The achievements of these models have been limited to a particular subset of domains where this assumption yields good results, namely homogeneous domains that are characterized by style or texture differences. We tackle the challenging problem of image-to-image translation where the domains are defined by high-level shapes and contexts, as well as including significant clutter and heterogeneity. For this purpose, we introduce a novel GAN based on preserving intra-domain vector transformations in a latent space learned by a siamese network. The traditional GAN system introduced a discriminator network to guide the generator into generating images in the target domain. To this two-network system we add a third: a siamese network that guides the generator so that each original image shares semantics with its generated version. With this new three-network system, we no longer need to constrain the generators with the ubiquitous cycle-consistency restraint. As a result, the generators can learn mappings between more complex domains that differ from each other by large differences - not just style or texture.

cs.CV↗

arXiv2019

Generating and Aligning from Data Geometries with Generative Adversarial Networks

Unsupervised domain mapping has attracted substantial attention in recent years due to the success of models based on the cycle-consistency assumption. These models map between two domains by fooling a probabilistic discriminator, thereby matching the probability distributions of the real and generated data. Instead of this probabilistic approach, we cast the problem in terms of aligning the geometry of the manifolds of the two domains. We introduce the Manifold Geometry Matching Generative Adversarial Network (MGM GAN), which adds two novel mechanisms to facilitate GANs sampling from the geometry of the manifold rather than the density and then aligning two manifold geometries: (1) an importance sampling technique that reweights points based on their density on the manifold, making the discriminator only able to discern geometry and (2) a penalty adapted from traditional manifold alignment literature that explicitly enforces the geometry to be preserved. The MGM GAN leverages the manifolds arising from a pre-trained autoencoder to bridge the gap between formal manifold alignment literature and existing GAN work, and demonstrate the advantages of modeling the manifold geometry over its density.

cs.LG↗

arXiv2019

Out-of-Sample Extrapolation with Neuron Editing

While neural networks can be trained to map from one specific dataset to another, they usually do not learn a generalized transformation that can extrapolate accurately outside the space of training. For instance, a generative adversarial network (GAN) exclusively trained to transform images of black-haired men to blond-haired men might not have the same effect on images of black-haired women. This is because neural networks are good at generation within the manifold of the data that they are trained on. However, generating new samples outside of the manifold or extrapolating "out-of-sample" is a much harder problem that has been less well studied. To address this, we introduce a technique called neuron editing that learns how neurons encode an edit for a particular transformation in a latent space. We use an autoencoder to decompose the variation within the dataset into activations of different neurons and generate transformed data by defining an editing transformation on those neurons. By performing the transformation in a latent trained space, we encode fairly complex and non-linear transformations to the data with much simpler distribution shifts to the neuron's activations. We motivate our technique on an image domain and then move to our two main biological applications: removal of batch artifacts representing unwanted noise and modeling the effect of drug treatments to predict synergy between drugs.

q-bio.QM↗

arXiv2018

Geometry-Based Data Generation

Many generative models attempt to replicate the density of their input data. However, this approach is often undesirable, since data density is highly affected by sampling biases, noise, and artifacts. We propose a method called SUGAR (Synthesis Using Geometrically Aligned Random-walks) that uses a diffusion process to learn a manifold geometry from the data. Then, it generates new points evenly along the manifold by pulling randomly generated points into its intrinsic structure using a diffusion kernel. SUGAR equalizes the density along the manifold by selectively generating points in sparse areas of the manifold. We demonstrate how the approach corrects sampling biases and artifacts, while also revealing intrinsic patterns (e.g. progression) and relations in the data. The method is applicable for correcting missing data, finding hypothetical data points, and learning relationships between data features.

cs.LG↗

arXiv2018

MAGAN: Aligning Biological Manifolds

It is increasingly common in many types of natural and physical systems (especially biological systems) to have different types of measurements performed on the same underlying system. In such settings, it is important to align the manifolds arising from each measurement in order to integrate such data and gain an improved picture of the system. We tackle this problem using generative adversarial networks (GANs). Recently, GANs have been utilized to try to find correspondences between sets of samples. However, these GANs are not explicitly designed for proper alignment of manifolds. We present a new GAN called the Manifold-Aligning GAN (MAGAN) that aligns two manifolds such that related points in each measurement space are aligned together. We demonstrate applications of MAGAN in single-cell biology in integrating two different measurement types together. In our demonstrated examples, cells from the same tissue are measured with both genomic (single-cell RNA-sequencing) and proteomic (mass cytometry) technologies. We show that the MAGAN successfully aligns them such that known correlations between measured markers are improved compared to other recently proposed models.

cs.CV↗