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Species tree estimation is frequently based on phylogenomic approaches that use multiple genes from throughout the genome. However, for a combination of reasons (ranging from sampling biases to more biological causes, as in gene birth and loss), gene trees are often incomplete, meaning that not all species of interest have a common set of genes. Incomplete gene trees can potentially impact the accuracy of phylogenomic inference. We, for the first time, introduce the problem of imputing the quartet distribution induced by a set of incomplete gene trees, which involves adding the missing quartets back to the quartet distribution. We present Quartet based Gene tree Imputation using Deep Learning (QT-GILD), an automated and specially tailored unsupervised deep learning technique, accompanied by cues from natural language processing, which learns the quartet distribution in a given set of incomplete gene trees and generates a complete set of quartets accordingly. QT-GILD is a general-purpose technique needing no explicit modeling of the subject system or reasons for missing data or gene tree heterogeneity. Experimental studies on a collection of simulated and empirical datasets suggest that QT-GILD can effectively impute the quartet distribution, which results in a dramatic improvement in the species tree accuracy. Remarkably, QT-GILD not only imputes the missing quartets but can also account for gene tree estimation error. Therefore, QT-GILD advances the state-of-the-art in species tree estimation from gene trees in the face of missing data.

Malaria, one of the leading causes of death in underdeveloped countries, is primarily diagnosed using microscopy. Computer-aided diagnosis of malaria is a challenging task owing to the fine-grained variability in the appearance of some uninfected and infected class. In this paper, we transform a malaria parasite object detection dataset into a classification dataset, making it the largest malaria classification dataset (63,645 cells), and evaluate the performance of several state-of-the-art deep neural network architectures pretrained on both natural and medical images on this new dataset. We provide detailed insights into the variation of the dataset and qualitative analysis of the results produced by the best models. We also evaluate the models using an independent test set to demonstrate the model's ability to generalize in different domains. Finally, we demonstrate the effect of conditional image synthesis on malaria parasite detection. We provide detailed insights into the influence of synthetic images for the class imbalance problem in the malaria diagnosis context., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

In recent years Deep Learning has brought about a breakthrough in Medical Image Segmentation. In this regard, U-Net has been the most popular architecture in the medical imaging community. Despite outstanding overall performance in segmenting multimodal medical images, through extensive experimentations on some challenging datasets, we demonstrate that the classical U-Net architecture seems to be lacking in certain aspects. Therefore, we propose some modifications to improve upon the already state-of-the-art U-Net model. Following these modifications, we develop a novel architecture, MultiResUNet, as the potential successor to the U-Net architecture. We have tested and compared MultiResUNet with the classical U-Net on a vast repertoire of multimodal medical images. Although only slight improvements in the cases of ideal images are noticed, remarkable gains in performance have been attained for the challenging ones. We have evaluated our model on five different datasets, each with their own unique challenges, and have obtained a relative improvement in performance of 10.15%, 5.07%, 2.63%, 1.41%, and 0.62% respectively. We have also discussed and highlighted some qualitatively superior aspects of MultiResUNet over classical U-Net that are not really reflected in the quantitative measures., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

CRISPR Cas-9 is a groundbreaking genome-editing tool that harnesses bacterial defense systems to alter DNA sequences accurately. This innovative technology holds vast promise in multiple domains like biotechnology, agriculture and medicine. However, such power does not come without its own peril, and one such issue is the potential for unintended modifications (Off-Target), which highlights the need for accurate prediction and mitigation strategies. Though previous studies have demonstrated improvement in Off-Target prediction capability with the application of deep learning, they often struggle with the precision-recall trade-off, limiting their effectiveness and do not provide proper interpretation of the complex decision-making process of their models. To address these limitations, we have thoroughly explored deep learning networks, particularly the recurrent neural network based models, leveraging their established success in handling sequence data. Furthermore, we have employed genetic algorithm for hyperparameter tuning to optimize these models' performance. The results from our experiments demonstrate significant performance improvement compared with the current state-of-the-art in Off-Target prediction, highlighting the efficacy of our approach. Furthermore, leveraging the power of the integrated gradient method, we make an effort to interpret our models resulting in a detailed analysis and understanding of the underlying factors that contribute to Off-Target predictions, in particular the presence of two sub-regions in the seed region of single guide RNA which extends the established biological hypothesis of Off-Target effects. To the best of our knowledge, our model can be considered as the first model combining high efficacy, interpretability and a desirable balance between precision and recall. [ABSTRACT FROM AUTHOR]

Lysine succinylation is a kind of post-translational modification (PTM) that plays a crucial role in regulating the cellular processes. Aberrant succinylation may cause inflammation, cancers, metabolism diseases and nervous system diseases. The experimental methods to detect succinylation sites are time-consuming and costly. This thus calls for computational models with high efficacy, and attention has been given in the literature to develop such models, albeit with only moderate success in the context of different evaluation metrics. One crucial aspect in this context is the biochemical and physicochemical properties of amino acids, which appear to be useful as features for such computational predictors. However, some of the existing computational models did not use the biochemical and physicochemical properties of amino acids. In contrast, some others used them without considering the inter-dependency among the properties. The combinations of biochemical and physicochemical properties derived through our optimization process achieve better results than the results achieved by combining all the properties. We propose three deep learning architectures: CNN+Bi-LSTM (CBL), Bi-LSTM+CNN (BLC) and their combination (CBL_BLC). We find that CBL_BLC outperforms the other two. Ensembling of different models successfully improves the results. Notably, tuning the threshold of the ensemble classifiers further improves the results. Upon comparing our work with other existing works on two datasets, we successfully achieve better sensitivity and specificity by varying the threshold value. [ABSTRACT FROM AUTHOR]

• Proposed dataset is one of the largest in blood cell segmentation domain. • Learning based algorithm outperforms non-learning based methods in both qualitative and quantitative aspect. • Although Otsu's method demonstrated competitive results in blood segmentation, but it failed to segment low contrast images. With the recent developments in deep learning, automatic cell segmentation from images of microscopic examination slides seems to be a solved problem as recent methods have achieved comparable results on existing benchmark datasets. However, most of the existing cell segmentation benchmark datasets either contain a single cell type, few instances of the cells, not publicly available. Therefore, it is unclear whether the performance improvements can generalize on more diverse datasets. In this paper, we present a large and diverse cell segmentation dataset BBBC041Seg 1 1 https://github.com/Deponker/Blood-cell-segmentation-dataset , which consists both of uninfected cells (i.e., red blood cells/RBCs, leukocytes) and infected cells (i.e., gametocytes, rings, trophozoites, and schizonts). Additionally, all cell types do not have equal instances, which encourages researchers to develop algorithms for learning from imbalanced classes in a few shot learning paradigm. Furthermore, we conduct a comparative study using both classical rule-based and recent deep learning state-of-the-art (SOTA) methods for automatic cell segmentation and provide them as strong baselines. We believe the introduction of BBBC041Seg will promote future research towards clinically applicable cell segmentation methods from microscopic examinations, which can be later used for downstream tasks such as detecting hematological diseases (i.e., malaria). [ABSTRACT FROM AUTHOR]