Genomic Sequencing News and Research

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Location of epigenetic changes co-locate with genetic signal causing psychartric disorder

Location of epigenetic changes co-locate with genetic signal causing psychartric disorder

Scientists solve mystery of Yemen cholera epidemic

Scientists solve mystery of Yemen cholera epidemic

Genetic testing can help personalize diagnosis and treatment of kidney disease, study shows

Genetic testing can help personalize diagnosis and treatment of kidney disease, study shows

Change in genome of Caucasians could explain higher rates of esophageal cancer

Change in genome of Caucasians could explain higher rates of esophageal cancer

New research collaboration launches first evolutionary study to explore origins of fish that walk

New research collaboration launches first evolutionary study to explore origins of fish that walk

TGen receives PayPal grant to underwrite costs of genetic tests for children with rare disorders

TGen receives PayPal grant to underwrite costs of genetic tests for children with rare disorders

Research team identifies Ashkenazi Jewish founder mutation for Leigh syndrome

Research team identifies Ashkenazi Jewish founder mutation for Leigh syndrome

Tracking down microRNA candidates linked to disease

Tracking down microRNA candidates linked to disease

Study offers new hope to patients with rare brain cancer

Study offers new hope to patients with rare brain cancer

Study pinpoints new marker that can predict Crohn’s disease subtype

Study pinpoints new marker that can predict Crohn’s disease subtype

15 promising technologies that could limit global catastrophic biological risks

15 promising technologies that could limit global catastrophic biological risks

TGen-UNM consortium awarded NIH grant to discover new treatments for diabetic blindness

TGen-UNM consortium awarded NIH grant to discover new treatments for diabetic blindness

TGen and PNOC take part in launch of NIH-supported Kids First Data Resource Portal

TGen and PNOC take part in launch of NIH-supported Kids First Data Resource Portal

Brigham Genomic Medicine program unravels 30 medical mysteries

Brigham Genomic Medicine program unravels 30 medical mysteries

KKH develops new test to enable faster diagnosis of critically ill children with rare diseases

KKH develops new test to enable faster diagnosis of critically ill children with rare diseases

Genetic variants impact outcome in dilated cardiomyopathy patients of African ancestry

Genetic variants impact outcome in dilated cardiomyopathy patients of African ancestry

Researchers identify genes responsible for inherited breast cancer in Nigerian women

Researchers identify genes responsible for inherited breast cancer in Nigerian women

Discovery may help broaden the scope of defenses against HPV

Discovery may help broaden the scope of defenses against HPV

Experts advise against universal genomic screening of newborns

Experts advise against universal genomic screening of newborns

Report discusses whether all newborns should undergo genetic sequencing

Report discusses whether all newborns should undergo genetic sequencing