To address food security challenges and climate change, the polyploid wild rice Oryza alta has been explored as a potential crop, although it suffers from seed shattering. We employed mesoporous
Magnetic nanoparticles (MNPs), due to their magnetic properties, can be activated by alternating magnetic field heating or unheated low frequency magnetic fields, thereby exerting intrinsic therapeutic effects or promoting drug
This study aims to perform a prenatal genetic diagnosis of a high-risk fetus with trisomy 7 identified by noninvasive prenatal testing (NIPT) and to evaluate the efficacy of different genetic
As the demand for WES increases and the cost of NGS decreases, WES, as a technique, requires a generous understanding of how experimental design can improve data interpretation and thus
GeneMind has collaborated with QIAGEN to validate multiple mature NGS solutions from QIAGEN based on the GeneMind SURFSeq 5000* and GenoLab M* sequencing platforms. The test results demonstrate high compatibility between the GeneMind sequencing platforms and
Genetic sequencers in modern molecular diagnostics and research employ Next-generation Sequencing tests to decode DNA or RNA sequences. Hence, they enable precise genetic analysis for disease diagnosis, personalized medicine, and evolutionary
IgG4-related disease (IgG4-RD) has complex clinical manifestations ranging from fibrosis and inflammation to deregulated metabolism. The molecular mechanisms underpinning these phenotypes are unclear. To investigate the transcriptomic changes in IgG4-RD
In this study, transcriptome sequencing of the whole fermentation course was perf ormed to explore the synthesis and regulation mechanism of AprE in B. licheniformis AQ. During the fermentation process,
The purpose of this study was to compare the chloroplast genomes of T. sinskajae and T. monococcum accession k-20970 and clarify the phylogenetic relationships between einkorn wheats via GeneMind GenoLab M
Targeted genomic sequencing (TS) greatly benefits precision oncology by rapidly detecting genetic variations with better accuracy and sensitivity owing to its high sequencing depth. Multiple sequencing platforms and variant calling
