The single nucleotide variation (SNV) assay holds significant value in the diagnosis of
genetic diseases. However, the wide application of SNV analysis in clinics meets many …

Single-nucleotide variant (SNV) is crucial in clinical diagnostics as a useful biomarker,
because it is closely associated with many diseases, such as genetic disorders and tumors …

Single-nucleotide variation (SNV) is a crucial biomarker for drug resistance-related detection
in cancer and bacterial infection. However, the unintended binding of DNA probes limits the …

Single nucleotide variant (SNV) has become an emerging biomarker for various diseases
such as cancers and infectious diseases. Toehold‐mediated strand displacement (TMSD) …

Single-nucleotide variants (SNVs) are the most common type variation of sequence
alterations at a specific location in the genome, thus involving significant clinical and …

Reliable, efficient and cost-effective modalities are urgently needed for mass screening of
gene mutations. Previous reports have shown that SSCP or genechip methods require …

In this study, we firstly propose a novel smartphone-assisted visualization SNP genotyping
method termed competitive activation cross amplification (CACA). The mutation detection …

Detection of single nucleotide polymorphisms (SNPs) is a crucial challenge in the
development of a novel generation of diagnostic tools. Accurate detection of SNPs can …

Single-nucleotide variation (SNV) detection plays significant roles in disease diagnosis and
treatment. Generally, auxiliary probe, restricted design rules, complicated detection system …

Sensitive and accurate identification of single-nucleotide mutations (SNMs) has become
crucial in the field of molecular diagnosis and personalized medicine. Here, we developed a …