SIP: A computational prediction of S-Adenosyl methionine (SAM) interacting proteins and their interaction sites through primary structures.

S-Adenosyl methionine (SAM), a universal methyl group donor, plays a vital role in biosynthesis and acts as an inhibitor to many enzymes. Due to protein interaction-dependent biological role, SAM has become a favorite target in various therapeutical and clinical studies such as treating cancer, Alzheimer's, epilepsy, and neurological disorders. Therefore, the identification of the SAM interacting proteins and their interaction sites is a biologically significant problem. However, wet-lab techniques, though accurate, to identify SAM interactions and interaction sites are tedious and costly. Therefore, efficient and accurate computational methods for this purpose are vital to the design and assist such wet-lab experiments. In this study, we present machine learning-based models to predict SAM interacting proteins and their interaction sites by using only primary structures of proteins. Here we modeled SAM interaction prediction through whole protein sequence features along with different classifiers. Whereas, we modeled SAM interaction site prediction through overlapping sequence windows and ranking with multiple instance learning that allows handling imprecisely annotated SAM interaction sites. Through a series of simulation studies along with biological significant evaluation, we showed that our proposed models give a state-of-the-art performance for both SAM interaction and interaction site prediction. Through data mining in this study, we have also identified various characteristics of amino acid sub-sequences and their relative position to effectively locate interaction sites in a SAM interacting protein. Python code for training and evaluating our proposed models together with a webserver implementation as SIP (Sam Interaction Predictor) is available at the URL: https://sites.google.com/view/wajidarshad/software.

COVIDC: An expert system to diagnose COVID-19 and predict its severity using chest CT scans: Application in radiology.

Early diagnosis of Coronavirus disease 2019 (COVID-19) is significantly important, especially in the absence or inadequate provision of a specific vaccine, to stop the surge of this lethal infection by advising quarantine. This diagnosis is challenging as most of the patients having COVID-19 infection stay asymptomatic while others showing symptoms are hard to distinguish from patients having different respiratory infections such as severe flu and Pneumonia. Due to cost and time-consuming wet-lab diagnostic tests for COVID-19, there is an utmost requirement for some alternate, non-invasive, rapid, and discounted automatic screening system. A chest CT scan can effectively be used as an alternative modality to detect and diagnose the COVID-19 infection. In this study, we present an automatic COVID-19 diagnostic and severity prediction system called COVIDC (COVID-19 detection using CT scans) that uses deep feature maps from the chest CT scans for this purpose. Our newly proposed system not only detects COVID-19 but also predicts its severity by using a two-phase classification approach (COVID vs non-COVID, and COVID-19 severity) with deep feature maps and different shallow supervised classification algorithms such as SVMs and random forest to handle data scarcity. We performed a stringent COVIDC performance evaluation not only through 10-fold cross-validation and an external validation dataset but also in a real setting under the supervision of an experienced radiologist. In all the evaluation settings, COVIDC outperformed all the existing state-of-the-art methods designed to detect COVID-19 with an F1 score of 0.94 on the validation dataset and justified its use to diagnose COVID-19 effectively in the real setting by classifying correctly 9 out of 10 COVID-19 CT scans. We made COVIDC openly accessible through a cloud-based webserver and python code available at https://sites.google.com/view/wajidarshad/software and https://github.com/wajidarshad/covidc.