Analysis of the fairness of machine learning (ML) algorithms recently attracted many researchers' interest. Most ML methods show bias toward protected groups, which limits the applicability of ML models in many applications like crime rate prediction etc. Since the data may have missing values which, if not appropriately handled, are known to further harmfully affect fairness. Many imputation methods are proposed to deal with missing data. However, the effect of missing data imputation on fairness is not studied well. In this paper, we analyze the effect on fairness in the context of graph data (node attributes) imputation using different embedding and neural network methods. Extensive experiments on six datasets demonstrate severe fairness issues in missing data imputation under graph node classification. We also find that the choice of the imputation method affects both fairness and accuracy. Our results provide valuable insights into graph data fairness and how to handle missingness in graphs efficiently. This work also provides directions regarding theoretical studies on fairness in graph data.
SARS-CoV-2, like any other virus, continues to mutate as it spreads, according to an evolutionary process. Unlike any other virus, the number of currently available sequences of SARS-CoV-2 in public databases such as GISAID is already several million. This amount of data has the potential to uncover the evolutionary dynamics of a virus like never before. However, a million is already several orders of magnitude beyond what can be processed by the traditional methods designed to reconstruct a virus's evolutionary history, such as those that build a phylogenetic tree. Hence, new and scalable methods will need to be devised in order to make use of the ever increasing number of viral sequences being collected. Since identifying variants is an important part of understanding the evolution of a virus, in this paper, we propose an approach based on clustering sequences to identify the current major SARS-CoV-2 variants. Using a $k$-mer based feature vector generation and efficient feature selection methods, our approach is effective in identifying variants, as well as being efficient and scalable to millions of sequences. Such a clustering method allows us to show the relative proportion of each variant over time, giving the rate of spread of each variant in different locations -- something which is important for vaccine development and distribution. We also compute the importance of each amino acid position of the spike protein in identifying a given variant in terms of information gain. Positions of high variant-specific importance tend to agree with those reported by the USA's Centers for Disease Control and Prevention (CDC), further demonstrating our approach.
Graph feature extraction is a fundamental task in graphs analytics. Using feature vectors (graph descriptors) in tandem with data mining algorithms that operate on Euclidean data, one can solve problems such as classification, clustering, and anomaly detection on graph-structured data. This idea has proved fruitful in the past, with spectral-based graph descriptors providing state-of-the-art classification accuracy on benchmark datasets. However, these algorithms do not scale to large graphs since: 1) they require storing the entire graph in memory, and 2) the end-user has no control over the algorithm's runtime. In this paper, we present single-pass streaming algorithms to approximate structural features of graphs (counts of subgraphs of order $k \geq 4$). Operating on edge streams allows us to avoid keeping the entire graph in memory, and controlling the sample size enables us to control the time taken by the algorithm. We demonstrate the efficacy of our descriptors by analyzing the approximation error, classification accuracy, and scalability to massive graphs. Our experiments showcase the effect of the sample size on approximation error and predictive accuracy. The proposed descriptors are applicable on graphs with millions of edges within minutes and outperform the state-of-the-art descriptors in classification accuracy.
With the rapid spread of the novel coronavirus (COVID-19) across the globe and its continuous mutation, it is of pivotal importance to design a system to identify different known (and unknown) variants of SARS-CoV-2. Identifying particular variants helps to understand and model their spread patterns, design effective mitigation strategies, and prevent future outbreaks. It also plays a crucial role in studying the efficacy of known vaccines against each variant and modeling the likelihood of breakthrough infections. It is well known that the spike protein contains most of the information/variation pertaining to coronavirus variants. In this paper, we use spike sequences to classify different variants of the coronavirus in humans. We show that preserving the order of the amino acids helps the underlying classifiers to achieve better performance. We also show that we can train our model to outperform the baseline algorithms using only a small number of training samples ($1\%$ of the data). Finally, we show the importance of the different amino acids which play a key role in identifying variants and how they coincide with those reported by the USA's Centers for Disease Control and Prevention (CDC).
Electromyography (EMG) signals have been successfully employed for driving prosthetic limbs of a single or double degree of freedom. This principle works by using the amplitude of the EMG signals to decide between one or two simpler movements. This method underperforms as compare to the contemporary advances done at the mechanical, electronics, and robotics end, and it lacks intuition. Recently, research on myoelectric control based on pattern recognition (PR) shows promising results with the aid of machine learning classifiers. Using the approach termed as, EMG-PR, EMG signals are divided into analysis windows, and features are extracted for each window. These features are then fed to the machine learning classifiers as input. By offering multiple class movements and intuitive control, this method has the potential to power an amputated subject to perform everyday life movements. In this paper, we investigate the effect of the analysis window and feature selection on classification accuracy of different hand and wrist movements using time-domain features. We show that effective data preprocessing and optimum feature selection helps to improve the classification accuracy of hand movements. We use publicly available hand and wrist gesture dataset of $40$ intact subjects for experimentation. Results computed using different classification algorithms show that the proposed preprocessing and features selection outperforms the baseline and achieve up to $98\%$ classification accuracy.