15k breast cancer patients a year could benefit from genome sequencing
Whole genome sequencing could identify unique genetic features to guide treatment for more than 15,000 breast cancer patients…
A Game-Changer in Genetics, But With
Recent advancements in artificial intelligence (AI) and DNA sequencing are pushing the boundaries of science and genetics, but…
Apollo Cancer Centres raises awareness on hereditary cancers
CHENNAI: Apollo Cancer Centres (ACC) has launched an initiative during Hereditary Cancer Awareness Week to create awareness about…
CHD8 in Cerebellar Function and Autism
Autism spectrum disorder (ASD) is a developmental disability caused by differences in the brain and affects ~1 in…
For high cholesterol, don’t blame genetics. Delhi cardiologist advises 3 immediate but simple changes to slash heart risk
Think high cholesterol is just in your genes? Think again. Delhi cardiologist Dr Shailesh Singh is calling out…
Fast, Precise Search in Petabase Sequence Data
In the rapidly evolving field of genomics, the ability to efficiently store, compress, and search vast quantities of…
Study finds women have higher genetic risk of depression
SYDNEY: Women are genetically at higher risk of clinical depression than men, Australian researchers found in a study…
Family fights to keep baby with rare genetic disorder alive
Pohamara, 37, told the Herald “the slightest infection could be fatal”. Katana Morunga was diagnosed with the genetic…
Rising Demand for Portable Genetic Testing Drives 15% CAGR Growth – FMIBlog
The global Handheld DNA Reader Market is set for remarkable growth, with a projected value increase from USD…
Largest study of African American brain tissue reveals key Alzheimer gene activity
The prevalence of Alzheimer disease (AD) is approximately two times higher in African Americans (AA) compared to White/European-ancestry…
Cytometric and genetic analysis of Slovenian local apple genotypes | BMC Plant Biology
SSR polymorphism and genetic diversity In this study, a total number of 233 apple genotypes were genotyped using…
Researchers identify novel CD46 gene mutation underlying aHUS
A never-before-reported mutation in the CD46 gene was found to contribute to the development of atypical hemolytic uremic syndrome…