AIMC Topic: Software

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Epitome: predicting epigenetic events in novel cell types with multi-cell deep ensemble learning.

Nucleic acids research
The accumulation of large epigenomics data consortiums provides us with the opportunity to extrapolate existing knowledge to new cell types and conditions. We propose Epitome, a deep neural network that learns similarities of chromatin accessibility ...

CellProfiler Analyst 3.0: accessible data exploration and machine learning for image analysis.

Bioinformatics (Oxford, England)
SUMMARY: Image-based experiments can yield many thousands of individual measurements describing each object of interest, such as cells in microscopy screens. CellProfiler Analyst is a free, open-source software package designed for the exploration of...

PreTP-EL: prediction of therapeutic peptides based on ensemble learning.

Briefings in bioinformatics
Therapeutic peptides are important for understanding the correlation between peptides and their therapeutic diagnostic potential. The therapeutic peptides can be further divided into different types based on therapeutic function sharing different cha...

Improved protein contact prediction using dimensional hybrid residual networks and singularity enhanced loss function.

Briefings in bioinformatics
Deep residual learning has shown great success in protein contact prediction. In this study, a new deep residual learning-based protein contact prediction model was developed. Comparing with previous models, a new type of residual block hybridizing 1...

Learning to SMILES: BAN-based strategies to improve latent representation learning from molecules.

Briefings in bioinformatics
Computational methods have become indispensable tools to accelerate the drug discovery process and alleviate the excessive dependence on time-consuming and labor-intensive experiments. Traditional feature-engineering approaches heavily rely on expert...

RefRGim: an intelligent reference panel reconstruction method for genotype imputation with convolutional neural networks.

Briefings in bioinformatics
Genotype imputation is a statistical method for estimating missing genotypes from a denser haplotype reference panel. Existing methods usually performed well on common variants, but they may not be ideal for low-frequency and rare variants. Previous ...

Integrative machine learning framework for the identification of cell-specific enhancers from the human genome.

Briefings in bioinformatics
Enhancers are deoxyribonucleic acid (DNA) fragments which when bound by transcription factors enhance the transcription of related genes. Due to its sporadic distribution and similar fractions, identification of enhancers from the human genome seems ...

Identifying complex motifs in massive omics data with a variable-convolutional layer in deep neural network.

Briefings in bioinformatics
Motif identification is among the most common and essential computational tasks for bioinformatics and genomics. Here we proposed a novel convolutional layer for deep neural network, named variable convolutional (vConv) layer, for effective motif ide...

Predicting MHC class I binder: existing approaches and a novel recurrent neural network solution.

Briefings in bioinformatics
Major histocompatibility complex (MHC) possesses important research value in the treatment of complex human diseases. A plethora of computational tools has been developed to predict MHC class I binders. Here, we comprehensively reviewed 27 up-to-date...

A novel antibacterial peptide recognition algorithm based on BERT.

Briefings in bioinformatics
As the best substitute for antibiotics, antimicrobial peptides (AMPs) have important research significance. Due to the high cost and difficulty of experimental methods for identifying AMPs, more and more researches are focused on using computational ...