Latest AI and machine learning research in genetics for healthcare professionals.
An early and accurate pregnancy diagnosis method is required to improve the reproductive performance...
Single-cell RNA sequencing (scRNA-seq) data has been widely used to profile cellular heterogeneities...
Acquired immune deficiency syndrome (AIDS) is a fatal disease caused by human immunodeficiency virus...
The purpose of this study was to detect the presence of retinitis pigmentosa (RP) based on color fun...
BACKGROUND: The all-electronic Single Molecule Break Junction (SMBJ) method is an emerging alternati...
BACKGROUND: Analyzing single-cell RNA sequencing (scRNAseq) data plays an important role in understa...
The primary sequences of DNA, RNA and protein have been used as the dominant information source of e...
The recent deluge of genome-wide technologies for the mapping of the epigenome and resulting data in...
Current understanding of the underlying molecular network and mechanism for attention-deficit hypera...
Venous thromboembolism is the third common cardiovascular disease and is composed of two entities, d...
PURPOSE: Roughly 70% of suspected Mendelian disease patients remain undiagnosed after genome sequenc...
In the detection of genome variation, the research on the internal correlation of reference genome i...
A reconfigurable biosensor with different spectral sensitivities could provide new opportunities to ...
Combining microfluidics technology with machine learning represents an innovative approach to conduc...
Segmentation and mutant classification of high-frequency ultrasound (HFU) mouse embryo brain ventric...
Recent studies suggest that epi-transcriptome regulation via post-transcriptional RNA modifications ...
It is a common paradigm in object detection frameworks that the samples in training and testing have...
Oligonucleotide-based aptamers, which have a three-dimensional structure with a single-stranded frag...
A major concern in the clinical application of cell therapy is the manufacturing cost of cell produc...
BACKGROUND AND OBJECTIVE: Mutations in the gene cause frontotemporal dementia (FTD). Most previous ...
Structure prediction for proteins lacking homologous templates in the Protein Data Bank (PDB) remain...