The cause of rare diseases is increasingly being detected through genome sequencing, which involves reading the entire human DNA by first breaking it into small pieces -- short reads. Scientists found ...

Genetic sequencing has gone through several advances. A major breakthrough came when scientists began breaking the billions ...

Information on tumor mutational status was limited before the development of NGS because traditional Sanger sequencing and ...

You began when egg and sperm met, and the DNA from your biological parents teamed up. Your first cell began copying its newly ...

The European consortium for Solving the Unsolved Rare Diseases has demonstrated the significance of international ...

( MENAFN - EIN Presswire) The post-harvest treatment market is expected to grow at a compound annual growth rate of 6.75% evaluated at US$2 billion in 2025.

India, a land of vast cultural and genetic diversity, has embarked on an ambitious scientific journey to explore its genetic ...

The PEACE-1 trial (NCT01957436) revealed that adding radiotherapy to standard of care (SOC) and abiraterone significantly ...

Morphological profiling allows accurate identification of cell types in dense iPSC-derived cultures, allowing its use for quality control and differentiation monitoring.

Improved medical treatments for Emiratis could be the result of a major project researching the genetic variation within the ...