Latest AI and machine learning research in genetics for healthcare professionals.
BACKGROUND: Nanopore-based DNA sequencing relies on basecalling the electric current signal. Basecal...
Discovering DNA regulatory sequence motifs and their relative positions is vital to understanding th...
The study of psoriasis has yielded fundamental new insights into immunologic regulation and innovati...
Breast cancer is the most common malignancy in women, with over 40,000 deaths annually in the United...
CRISPR/Cas9 technology is capable of precisely editing genomes and is at the heart of various scient...
The binding of DNA sequences to cell type-specific transcription factors is essential for regulating...
Cell type identification from single-cell transcriptomic data is a common goal of single-cell RNA se...
DNA-binding proteins (DBPs) have a significant impact on many life activities, so identification of ...
Proteins binding to Ribonucleic Acid (RNA) inside cells are called RNA-binding proteins (RBP), which...
Previous models have shown that learning drug features from their graph representation is more effic...
Synthetic biology has made it possible to rewire natural cellular responses to treat disease, notabl...
As synthetic biology expands and accelerates into real-world applications, methods for quantitativel...
RNA-binding proteins (RBPs) play significant roles in many biological life activities, many algorith...
With the continuous development of information technology and the running speed of computers, the de...
We present a deep-learning-based platform, MIND-S, for protein post-translational modification (PTM)...
Interpretation of noncoding genomic variants is one of the most important challenges in human geneti...
Machine learning models have difficulty generalizing to data outside of the distribution they were t...
The COVID-19 pandemic has presented an unprecedented challenge to the healthcare system. Identifying...
Tat is an essential gene for increasing the transcription of all HIV genes, and affects HIV replicat...
Structural variants (SVs) are a major driver of genetic diversity and disease in the human genome an...
Genetic variations are one of the major causes of phenotypic variations between human individuals. A...