Exome Sequencing News and Research

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Ingenuity Variant Analysis and iReport selected for Weill Cornell sequencing core facility

Ingenuity Variant Analysis and iReport selected for Weill Cornell sequencing core facility

WUSTL scientists to decode DNA of 99 patients with rare diseases

WUSTL scientists to decode DNA of 99 patients with rare diseases

Oxford Gene Technology develops optimised rare disease sequencing and analysis service

Oxford Gene Technology develops optimised rare disease sequencing and analysis service

BGI and VIB's genomics meeting to take place on Feb. 15

BGI and VIB's genomics meeting to take place on Feb. 15

Whole exome sequencing provides clues about rare mutations in aneurysms

Whole exome sequencing provides clues about rare mutations in aneurysms

Whole-exome sequencing discovers cause of glycosylation disorders

Whole-exome sequencing discovers cause of glycosylation disorders

Cancer Genomics now available online

Cancer Genomics now available online

Researchers discover new mechanism that regulates blood pressure

Researchers discover new mechanism that regulates blood pressure

TRON uses Ingenuity Variant Analysis to identify cancer driver variants

TRON uses Ingenuity Variant Analysis to identify cancer driver variants

Next generation personal genomic testing now widely available

Next generation personal genomic testing now widely available

Scientists discover new candidate gene for Dravet syndrome

Scientists discover new candidate gene for Dravet syndrome

Ambry to use Agilent SureSelect Target Enrichment System for exome sequencing

Ambry to use Agilent SureSelect Target Enrichment System for exome sequencing

GeneDx launches new genetic test to accurately diagnose rare diseases

GeneDx launches new genetic test to accurately diagnose rare diseases

Life Technologies launches Ion AmpliSeq Cancer Panel

Life Technologies launches Ion AmpliSeq Cancer Panel

Researchers discover new inherited disorder that causes mental retardation, liver dysfunction

Researchers discover new inherited disorder that causes mental retardation, liver dysfunction

Ambry to provide CLIA-approved exome services for applications in clinical diagnostics

Ambry to provide CLIA-approved exome services for applications in clinical diagnostics

Axeq announces Turnkey Discovery sequencing and analysis services

Axeq announces Turnkey Discovery sequencing and analysis services

Fast-track genetic diagnosis for hearing loss

Fast-track genetic diagnosis for hearing loss

Research identifies 6 critical deafness-related mutations in Israeli Jewish, Palestinian Arab families

Research identifies 6 critical deafness-related mutations in Israeli Jewish, Palestinian Arab families

Studies reveal new set of mutations linked with head and neck cancer

Studies reveal new set of mutations linked with head and neck cancer

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