New research by UCLA Health has identified a sex-chromosome linked gene that drives inflammation in the female brain, ...

The genetic roots of a disease or disorder do not always grow into clear cut, easily diagnosed clinical features.

Your DNA contains millions of genetic variants that interact with each other in ways that affect whether diseases such as ...

Veg Spring Rolls - Vegetables Spring Rolls - Easy & Quick Snack Recipe Nag Ashwin Shares Cryptic Note After Deepika Padukone’s Exit From Kalki 2: ‘Can’t Change What Happened’ Nepal ex-PM Oli takes ...

Env: Sniffles 2.6.3, hg38, long-read data. Problem: For sequence-resolved PRECISE deletions, Sniffles writes END that is 1 bp shorter than expected. len(REF) = 92, so the deleted length L = 91, which ...

Mutations in FMR1, the gene encoding fragile X messenger ribonucleoprotein 1 (FMRP), located at Xq27.3 and discovered in 1991, are the leading single-gene causes of autism and intellectual disability.

Toward a Computable Phenotype for Determining Eligibility of Lung Cancer Screening Using Electronic Health Records Somatic mutations in HLA genes were detected in the tumor data of five patients, and ...

Biological science has made such astonishing leaps in the last few decades, such as precise gene editing, that scientists are now tackling the next logical — yet inherently controversial — step: ...

Chitra Kannabiran, PhD, Kallam Anji Reddy Molecular Genetics Laboratory, Hyderabad Eye Research Foundation, Champalimaud Translational Centre, LV Prasad Eye Institute, Hyderabad 500 034, India ...

Copine-6 is a calcium-sensitive phospholipid-binding protein of the evolutionarily conserved Copine family. In the central nervous system, Copine-6 regulates function of some neurotransmitter ...