More Like this

1. Triplet Fingerprinting: More Practical and Portable Website Fingerprinting with N-shot Learning

   https://doi.org/10.1145/3319535.3354217  

   Sirinam, Payap ; Mathews, Nate ; Rahman, Mohammad Saidur ; Wright, Matthew ( November 2019 , CCS '19: Proceedings of the 2019 ACM SIGSAC Conference on Computer and Communications Security)

   Website Fingerprinting (WF) attacks pose a serious threat to users' online privacy, including for users of the Tor anonymity system. By exploiting recent advances in deep learning, WF attacks like Deep Fingerprinting (DF) have reached up to 98% accuracy. The DF attack, however, requires large amounts of training data that needs to be updated regularly, making it less practical for the weaker attacker model typically assumed in WF. Moreover, research on WF attacks has been criticized for not demonstrating attack effectiveness under more realistic and more challenging scenarios. Most research on WF attacks assumes that the testing and training data have similar distributions and are collected from the same type of network at about the same time. In this paper, we examine how an attacker could leverage N-shot learning---a machine learning technique requiring just a few training samples to identify a given class---to reduce the effort of gathering and training with a large WF dataset as well as mitigate the adverse effects of dealing with different network conditions. In particular, we propose a new WF attack called Triplet Fingerprinting (TF) that uses triplet networks for N-shot learning. We evaluate this attack in challenging settings such as where the training and testing data are collected multiple years apart on different networks, and we find that the TF attack remains effective in such settings with 85% accuracy or better. We also show that the TF attack is also effective in the open world and outperforms traditional transfer learning. On top of that, the attack requires only five examples to recognize a website, making it dangerous in a wide variety of scenarios where gathering and training on a complete dataset would be impractical. 

   more » « less
2. Adversarial Traces for Website Fingerprinting Defense

   https://doi.org/10.1145/3243734.3278493  

   Imani, Mohsen ; Rahman, Mohammad Saidur ; Wright, Matthew ( October 2018 , Proceedings of the 2018 ACM SIGSAC Conference on Computer and Communications Security)

   Website Fingerprinting (WF) is a traffic analysis attack that enables an eavesdropper to infer the victim's web activity even when encrypted and even when using the Tor anonymity system. Using deep learning classifiers, the attack can reach up to 98% accuracy. Existing WF defenses are either too expensive in terms of bandwidth and latency overheads (e.g. 2-3 times as large or slow) or ineffective against the latest attacks. In this work, we explore a novel defense based on the idea of adversarial examples that have been shown to undermine machine learning classifiers in other domains. Our Adversarial Traces defense adds padding to a Tor traffic trace in a manner that reliably fools the classifier into classifying it as coming from a different site. The technique drops the accuracy of the state-of-the-art attack from 98% to 60%, while incurring a reasonable 47% bandwidth overhead, showing its promise as a possible defense for Tor. 

   more » « less
3. Data-Explainable Website Fingerprinting with Network Simulation

   https://doi.org/10.56553/popets-2023-0125  

   Jansen, Rob ; Wails, Ryan ( October 2023 , Proceedings on Privacy Enhancing Technologies)

   Website fingerprinting (WF) attacks allow an adversary to associate a website with the encrypted traffic patterns produced when accessing it, thus threatening to destroy the client-server unlinkability promised by anonymous communication networks. Explainable WF is an open problem in which we need to improve our understanding of (1) the machine learning models used to conduct WF attacks; and (2) the WF datasets used as inputs to those models. This paper focuses on explainable datasets; that is, we develop an alternative to the standard practice of gathering low-quality WF datasets using synthetic browsers in large networks without controlling for natural network variability. In particular, we demonstrate how network simulation can be used to produce explainable WF datasets by leveraging the simulator's high degree of control over network operation. Through a detailed investigation of the effect of network variability on WF performance, we find that: (1) training and testing WF attacks in networks with distinct levels of congestion increases the false-positive rate by as much as 200%; (2) augmenting the WF attacks by training them across several networks with varying degrees of congestion decreases the false-positive rate by as much as 83%; and (3) WF classifiers trained on completely simulated data can achieve greater than 80% accuracy when applied to the real world.

    

   more » « less
4. The Temple University Digital Pathology Corpus: The Breast Tissue Subset

   https://doi.org/10.1109/SPMB52430.2021.9672275  

   Wevodau, Z. ; Doshna, B. ; Jhala, N. ; Akhtar, I. ; Obeid, I. ; Picone, J. ( December 2021 , Proceedings of the IEEE Signal Processing in Medicine and Biology Symposium (SPMB))

   Obeid, I. (Ed.)

   The Neural Engineering Data Consortium (NEDC) is developing the Temple University Digital Pathology Corpus (TUDP), an open source database of high-resolution images from scanned pathology samples [1], as part of its National Science Foundation-funded Major Research Instrumentation grant titled “MRI: High Performance Digital Pathology Using Big Data and Machine Learning” [2]. The long-term goal of this project is to release one million images. We have currently scanned over 100,000 images and are in the process of annotating breast tissue data for our first official corpus release, v1.0.0. This release contains 3,505 annotated images of breast tissue including 74 patients with cancerous diagnoses (out of a total of 296 patients). In this poster, we will present an analysis of this corpus and discuss the challenges we have faced in efficiently producing high quality annotations of breast tissue. It is well known that state of the art algorithms in machine learning require vast amounts of data. Fields such as speech recognition [3], image recognition [4] and text processing [5] are able to deliver impressive performance with complex deep learning models because they have developed large corpora to support training of extremely high-dimensional models (e.g., billions of parameters). Other fields that do not have access to such data resources must rely on techniques in which existing models can be adapted to new datasets [6]. A preliminary version of this breast corpus release was tested in a pilot study using a baseline machine learning system, ResNet18 [7], that leverages several open-source Python tools. The pilot corpus was divided into three sets: train, development, and evaluation. Portions of these slides were manually annotated [1] using the nine labels in Table 1 [8] to identify five to ten examples of pathological features on each slide. Not every pathological feature is annotated, meaning excluded areas can include focuses particular to these labels that are not used for training. A summary of the number of patches within each label is given in Table 2. To maintain a balanced training set, 1,000 patches of each label were used to train the machine learning model. Throughout all sets, only annotated patches were involved in model development. The performance of this model in identifying all the patches in the evaluation set can be seen in the confusion matrix of classification accuracy in Table 3. The highest performing labels were background, 97% correct identification, and artifact, 76% correct identification. A correlation exists between labels with more than 6,000 development patches and accurate performance on the evaluation set. Additionally, these results indicated a need to further refine the annotation of invasive ductal carcinoma (“indc”), inflammation (“infl”), nonneoplastic features (“nneo”), normal (“norm”) and suspicious (“susp”). This pilot experiment motivated changes to the corpus that will be discussed in detail in this poster presentation. To increase the accuracy of the machine learning model, we modified how we addressed underperforming labels. One common source of error arose with how non-background labels were converted into patches. Large areas of background within other labels were isolated within a patch resulting in connective tissue misrepresenting a non-background label. In response, the annotation overlay margins were revised to exclude benign connective tissue in non-background labels. Corresponding patient reports and supporting immunohistochemical stains further guided annotation reviews. The microscopic diagnoses given by the primary pathologist in these reports detail the pathological findings within each tissue site, but not within each specific slide. The microscopic diagnoses informed revisions specifically targeting annotated regions classified as cancerous, ensuring that the labels “indc” and “dcis” were used only in situations where a micropathologist diagnosed it as such. Further differentiation of cancerous and precancerous labels, as well as the location of their focus on a slide, could be accomplished with supplemental immunohistochemically (IHC) stained slides. When distinguishing whether a focus is a nonneoplastic feature versus a cancerous growth, pathologists employ antigen targeting stains to the tissue in question to confirm the diagnosis. For example, a nonneoplastic feature of usual ductal hyperplasia will display diffuse staining for cytokeratin 5 (CK5) and no diffuse staining for estrogen receptor (ER), while a cancerous growth of ductal carcinoma in situ will have negative or focally positive staining for CK5 and diffuse staining for ER [9]. Many tissue samples contain cancerous and non-cancerous features with morphological overlaps that cause variability between annotators. The informative fields IHC slides provide could play an integral role in machine model pathology diagnostics. Following the revisions made on all the annotations, a second experiment was run using ResNet18. Compared to the pilot study, an increase of model prediction accuracy was seen for the labels indc, infl, nneo, norm, and null. This increase is correlated with an increase in annotated area and annotation accuracy. Model performance in identifying the suspicious label decreased by 25% due to the decrease of 57% in the total annotated area described by this label. A summary of the model performance is given in Table 4, which shows the new prediction accuracy and the absolute change in error rate compared to Table 3. The breast tissue subset we are developing includes 3,505 annotated breast pathology slides from 296 patients. The average size of a scanned SVS file is 363 MB. The annotations are stored in an XML format. A CSV version of the annotation file is also available which provides a flat, or simple, annotation that is easy for machine learning researchers to access and interface to their systems. Each patient is identified by an anonymized medical reference number. Within each patient’s directory, one or more sessions are identified, also anonymized to the first of the month in which the sample was taken. These sessions are broken into groupings of tissue taken on that date (in this case, breast tissue). A deidentified patient report stored as a flat text file is also available. Within these slides there are a total of 16,971 total annotated regions with an average of 4.84 annotations per slide. Among those annotations, 8,035 are non-cancerous (normal, background, null, and artifact,) 6,222 are carcinogenic signs (inflammation, nonneoplastic and suspicious,) and 2,714 are cancerous labels (ductal carcinoma in situ and invasive ductal carcinoma in situ.) The individual patients are split up into three sets: train, development, and evaluation. Of the 74 cancerous patients, 20 were allotted for both the development and evaluation sets, while the remain 34 were allotted for train. The remaining 222 patients were split up to preserve the overall distribution of labels within the corpus. This was done in hope of creating control sets for comparable studies. Overall, the development and evaluation sets each have 80 patients, while the training set has 136 patients. In a related component of this project, slides from the Fox Chase Cancer Center (FCCC) Biosample Repository (https://www.foxchase.org/research/facilities/genetic-research-facilities/biosample-repository -facility) are being digitized in addition to slides provided by Temple University Hospital. This data includes 18 different types of tissue including approximately 38.5% urinary tissue and 16.5% gynecological tissue. These slides and the metadata provided with them are already anonymized and include diagnoses in a spreadsheet with sample and patient ID. We plan to release over 13,000 unannotated slides from the FCCC Corpus simultaneously with v1.0.0 of TUDP. Details of this release will also be discussed in this poster. Few digitally annotated databases of pathology samples like TUDP exist due to the extensive data collection and processing required. The breast corpus subset should be released by November 2021. By December 2021 we should also release the unannotated FCCC data. We are currently annotating urinary tract data as well. We expect to release about 5,600 processed TUH slides in this subset. We have an additional 53,000 unprocessed TUH slides digitized. Corpora of this size will stimulate the development of a new generation of deep learning technology. In clinical settings where resources are limited, an assistive diagnoses model could support pathologists’ workload and even help prioritize suspected cancerous cases. ACKNOWLEDGMENTS This material is supported by the National Science Foundation under grants nos. CNS-1726188 and 1925494. Any opinions, findings, and conclusions or recommendations expressed in this material are those of the author(s) and do not necessarily reflect the views of the National Science Foundation. REFERENCES [1] N. Shawki et al., “The Temple University Digital Pathology Corpus,” in Signal Processing in Medicine and Biology: Emerging Trends in Research and Applications, 1st ed., I. Obeid, I. Selesnick, and J. Picone, Eds. New York City, New York, USA: Springer, 2020, pp. 67 104. https://www.springer.com/gp/book/9783030368432. [2] J. Picone, T. Farkas, I. Obeid, and Y. Persidsky, “MRI: High Performance Digital Pathology Using Big Data and Machine Learning.” Major Research Instrumentation (MRI), Division of Computer and Network Systems, Award No. 1726188, January 1, 2018 – December 31, 2021. https://www. isip.piconepress.com/projects/nsf_dpath/. [3] A. Gulati et al., “Conformer: Convolution-augmented Transformer for Speech Recognition,” in Proceedings of the Annual Conference of the International Speech Communication Association (INTERSPEECH), 2020, pp. 5036-5040. https://doi.org/10.21437/interspeech.2020-3015. [4] C.-J. Wu et al., “Machine Learning at Facebook: Understanding Inference at the Edge,” in Proceedings of the IEEE International Symposium on High Performance Computer Architecture (HPCA), 2019, pp. 331–344. https://ieeexplore.ieee.org/document/8675201. [5] I. Caswell and B. Liang, “Recent Advances in Google Translate,” Google AI Blog: The latest from Google Research, 2020. [Online]. Available: https://ai.googleblog.com/2020/06/recent-advances-in-google-translate.html. [Accessed: 01-Aug-2021]. [6] V. Khalkhali, N. Shawki, V. Shah, M. Golmohammadi, I. Obeid, and J. Picone, “Low Latency Real-Time Seizure Detection Using Transfer Deep Learning,” in Proceedings of the IEEE Signal Processing in Medicine and Biology Symposium (SPMB), 2021, pp. 1 7. https://www.isip. piconepress.com/publications/conference_proceedings/2021/ieee_spmb/eeg_transfer_learning/. [7] J. Picone, T. Farkas, I. Obeid, and Y. Persidsky, “MRI: High Performance Digital Pathology Using Big Data and Machine Learning,” Philadelphia, Pennsylvania, USA, 2020. https://www.isip.piconepress.com/publications/reports/2020/nsf/mri_dpath/. [8] I. Hunt, S. Husain, J. Simons, I. Obeid, and J. Picone, “Recent Advances in the Temple University Digital Pathology Corpus,” in Proceedings of the IEEE Signal Processing in Medicine and Biology Symposium (SPMB), 2019, pp. 1–4. https://ieeexplore.ieee.org/document/9037859. [9] A. P. Martinez, C. Cohen, K. Z. Hanley, and X. (Bill) Li, “Estrogen Receptor and Cytokeratin 5 Are Reliable Markers to Separate Usual Ductal Hyperplasia From Atypical Ductal Hyperplasia and Low-Grade Ductal Carcinoma In Situ,” Arch. Pathol. Lab. Med., vol. 140, no. 7, pp. 686–689, Apr. 2016. https://doi.org/10.5858/arpa.2015-0238-OA. 

   more » « less
5. Training Faster by Separating Modes of Variation in Batch-normalized Models

   https://doi.org/10.1109/TPAMI.2019.2895781  

   Kalayeh, Mahdi M. ; Shah, Mubarak ( January 2019 , IEEE Transactions on Pattern Analysis and Machine Intelligence)

   Batch Normalization (BN) is essential to effectively train state-of-the-art deep Convolutional Neural Networks (CNN). It normalizes the layer outputs during training using the statistics of each mini-batch. BN accelerates training procedure by allowing to safely utilize large learning rates and alleviates the need for careful initialization of the parameters. In this work, we study BN from the viewpoint of Fisher kernels that arise from generative probability models. We show that assuming samples within a mini-batch are from the same probability density function, then BN is identical to the Fisher vector of a Gaussian distribution. That means batch normalizing transform can be explained in terms of kernels that naturally emerge from the probability density function that models the generative process of the underlying data distribution. Consequently, it promises higher discrimination power for the batch-normalized mini-batch. However, given the rectifying non-linearities employed in CNN architectures, distribution of the layer outputs show an asymmetric characteristic. Therefore, in order for BN to fully benefit from the aforementioned properties, we propose approximating underlying data distribution not with one, but a mixture of Gaussian densities. Deriving Fisher vector for a Gaussian Mixture Model (GMM), reveals that batch normalization can be improved by independently normalizing with respect to the statistics of disentangled sub-populations. We refer to our proposed soft piecewise version of batch normalization as Mixture Normalization (MN). Through extensive set of experiments on CIFAR-10 and CIFAR-100, using both a 5-layers deep CNN and modern Inception-V3 architecture, we show that mixture normalization reduces required number of gradient updates to reach the maximum test accuracy of the batch normalized model by ∼31%-47% across a variety of training scenarios. Replacing even a few BN modules with MN in the 48-layers deep Inception-V3 architecture is sufficient to not only obtain considerable training acceleration but also better final test accuracy. We show that similar observations are valid for 40 and 100-layers deep DenseNet architectures as well. We complement our study by evaluating the application of mixture normalization to the Generative Adversarial Networks (GANs), where "mode collapse" hinders the training process. We solely replace a few batch normalization layers in the generator with our proposed mixture normalization. Our experiments using Deep Convolutional GAN (DCGAN) on CIFAR-10 show that mixture normalized DCGAN not only provides an acceleration of ∼58% but also reaches lower (better) "Fréchet Inception Distance" (FID) of 33.35 compared to 37.56 of its batch normalized counterpart. 

   more » « less