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In the past centuries, scientists and thinkers alike have pondered the question of how our traits are passed down from generation to generation. What makes you, me, and me, me? The answer lies in the intricate web of inheritance, a puzzle that technology has been able to solve.In essence, the goal of this article is
As per the report by Fortune Business Insights, the global Genomics Market size is projected to reach USD 94.65 billion in 2028, at a CAGR of 19.4% during...
/PRNewswire/ -- In the near future, the clinical trials industry is poised to undergo a transformative evolution, marked by unprecedented advancements in...
Around 5.2% of the global population carries abnormal hemoglobin genes. Each year, 300,000 to 500,000 children are born with severe hemoglobinopathies worldwide, with approximately 80% of these cases occurring in developing countries.
Thalassemia is the most common hereditary hemoglobinopathy and occurs in 4.4 out of every 10,000 live births. It is prevalent in Mediterranean coastal areas, Africa, the Middle East, Southeast Asia, and southern China. This new study by Tong Yang, Xuemei Luo, Yanqiu Liu, Wenqian Zhang (BGI Genomics, Senior Manager Clinical Research) et al. published on August 18, 2023 in Human Genomics looks at the prevalence and mutation spectrum of thalassemia in Ganzhou based on a large-scale thalassemia screening project involving 136,312 individuals.