Latest AI and machine learning research in genetics for healthcare professionals.
Detecting gene-gene interactions in single-nucleotide polymorphism data is vital for understanding disease susceptibility. However, existing approaches may be limited by the sample size in case-control studies. Herein, we propose a balance approach for the multifactor dimensionality reduction (BMDR) method to increase the accuracy of estimates of the prediction error rate in small samples. BMDR ex...
Most past works for DNA-binding residue prediction did not consider the relationships between residues. In this paper, we propose a novel approach for DNA-binding residue prediction, referred to as EL_LSTM, which includes two main components. The first component is the Long Short-Term Memory (LSTM), which learns pairwise relationships between residues through a bi-gram model and then learns featur...
BACKGROUND: Although different quality controls have been applied at different stages of the sample preparation and data analysis to ensure both repro...
N- methyladenosine (mA) is a vital post-transcriptional modification, which adds another layer of epigenetic regulation at RNA level. It chemically mo...
The biological interpretation of gene lists with interesting shared properties, such as up- or down-regulation in a particular experiment, is typicall...
HIV resistance emerging against antiretroviral drugs represents a great threat to the continued prolongation of the lifespans of HIV-infected patients...
BACKGROUND & OBJECTIVE: is an opportunistic pathogen with high pathogenic and antibiotic-resistance potential and is also considered as one of the ma...
Key challenges for human genetics, precision medicine and evolutionary biology include deciphering the regulatory code of gene expression and understa...
BACKGROUND: Human genetic research has implicated functional variants of more than one hundred genes in the modulation of persisting pain. Artificial ...
Long noncoding RNAs (lncRNAs) are transcripts generally longer than 200 nucleotides with no or poor protein coding potential, and most of their functi...
A key challenge in precision medicine lies in understanding molecular-level underpinnings of complex human disease. Biological networks in multicellul...
BACKGROUND: An open challenge in translational bioinformatics is the analysis of sequenced metagenomes from various environmental samples. Of course, ...
OBJECTIVES: In the postneoadjuvant chemotherapy (NAC) setting, conventional radiographic complete response (rCR) is a poor predictor of pathologic com...
From bacteria following simple chemical gradients to the brain distinguishing complex odour information, the ability to recognize molecular patterns i...
Acute prediction of SNPs (Single Nucleotide Polymorphisms) from high throughput sequencing data is a challenging problem, having potential to explore ...
The interfacial region in composites that incorporate filler materials of dramatically different modulus relative to the resin phase acts as a stress ...
BACKGROUND: RNA regulation is significantly dependent on its binding protein partner, known as the RNA-binding proteins (RBPs). Unfortunately, the bin...
Second-generation DNA sequencing techniques generate short reads that can result in fragmented genome assemblies. Third-generation sequencing platform...
This paper demonstrates the ability of mach- ine learning approaches to identify a few genes among the 23,398 genes of the human genome to experiment ...
For more than a century, hematoxylin and eosin (H&E) staining has been the de facto standard for histological studies. Consequently, the legacy of his...