Genoseq Diagnostics

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Genoseq Dx a healthcare company focused on saving lives and improving health by pioneering new NGS technologies for early stages of rare, metabolic and neurodegenerative diseases.

Two days hands on training- adult stem cell culture techniques
05/10/2023

Two days hands on training- adult stem cell culture techniques

"May the colors and joy of Onam fill your life with happiness and prosperity! Wishing you a wonderful Onam celebration! ...
28/08/2023

"May the colors and joy of Onam fill your life with happiness and prosperity! Wishing you a wonderful Onam celebration! 🌼🌈 "

🚀 Exciting News! Our new website is LIVE! 🌐 Discover Unleashing the Future of Innovation today: www.genoseqdx.com. Join ...
24/08/2023

🚀 Exciting News! Our new website is LIVE! 🌐 Discover Unleashing the Future of Innovation today: www.genoseqdx.com. Join us in the search for answers about rare genetic disorder. Spread the word! Genoseq Diagnostics

Happy Doctor's day
01/07/2023

Happy Doctor's day

Scientists at EMBL Heidelberg have now shown how inversions are one of the most common mutational processes in humans.Th...
16/05/2022

Scientists at EMBL Heidelberg have now shown how inversions are one of the most common mutational processes in humans.
The team, in collaboration with scientists at University of Washington and Heinrich Heine University, investigated a set of 40 inversions that form recurrently in the human genome, where the DNA sequence may flip back and forth. The ‘flip-flopping’ inversions typically lie in regions commonly linked to development of certain genomic disorders.
Learn more with EMBL: https://www.embl.org/news/science/flip-flop-genome/

# Genoseq Diagnostics

Researchers at EMBL Heidelberg found that inversions in the human genome form more commonly than previously thought, which impacts our understanding of certain genetic diseases.

Inherited blood disorders can cause severe disruption in red and white blood cell function, leading to severe diseases s...
09/05/2022

Inherited blood disorders can cause severe disruption in red and white blood cell function, leading to severe diseases such as sickle cell anemia, beta thalassemia, and Fanconi anemia.

Gene therapy may be a key approach in treating blood disorders by ex vivo modification of the gene within red blood cells that lead to formation of these diseases.

Learn more with ASGCT! https://www.youtube.com/watch?v=zb3dIr20UV0

Sickle cell disease, beta thalassemia, and Fanconi anemia are a collection of inherited blood disorders caused by faulty genes that keep the elements of our ...

“Be Aware. Share. Care: Working with the global community as one to improve thalassaemia knowledge.’’Thalassemia is an i...
09/05/2022

“Be Aware. Share. Care: Working with the global community as one to improve thalassaemia knowledge.’’

Thalassemia is an inherited blood disorder which reduce the production of functional haemoglobin.
Alpha thalassemia ( genetic changes in HBA1 and HBA2) and Beta thalassemia ( genetic changes in HBB).


Normally, a cell needs to duplicate all its   so each new cell can receive a copy. This process usually occurs in the tw...
05/05/2022

Normally, a cell needs to duplicate all its so each new cell can receive a copy. This process usually occurs in the two extensively studied types of cell division, known as and .

For hundreds of years there have only been two main types of cell division in animals. But now researchers have identified a new and unexpected kind of cell ...

Ramadan Mubarak to you and your family
03/05/2022

Ramadan Mubarak to you and your family

"The world is incomplete without the contribution of labours as we are the one who work so hard to make the impossible p...
01/05/2022

"The world is incomplete without the contribution of labours as we are the one who work so hard to make the impossible possible".

Address

Near Vandalur Bypass Road
Chennai
600048

Opening Hours

Monday 9am - 7pm
Tuesday 9am - 7pm
Wednesday 9am - 7pm
Thursday 9am - 7pm
Friday 9am - 7pm
Saturday 9am - 7pm
Sunday 9am - 7pm

Telephone

+919150001024

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