NGS and Sanger Sequencing Go Hand in Hand for Genetic Analysis

SNPs and Human Diseases SNPs, single nucleotide polymorphism, is the simplest genetic variation and occurs in every 1000 bases in human genomic DNA. Among the 3.5 million SNPs, some lie in intergenic regions (non-coding regions that play regulatory roles) while others...

GWAS and WES as Gene Discovery Tools for Parkinson Diseases

Parkinson Disease: a common neurodegenerative disorder Parkinson diseases (PD) is the second most common neurodegenerative disorder that usually has a late onset; it affects 1% of the population over age 60 and a total 4million people in the globe. The people with PD...

The Role of Sanger Sequencing in COVID-19 Variant Detection

Covid-19 and Variants of Concern Since its first occurrence in 2019, COVID-19 has been spreading globally infecting close to 165 million people and having killed more than 3.4 million people as of May19, 2021. The CDC has recommended self-protection measures such as...