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Claritas Genomics announces launch of Claritas Clinical Exome, novel diagnostic test

Claritas Genomics announces launch of Claritas Clinical Exome, novel diagnostic test

Jumping genes: a marker for early cancer diagnosis? An interview with Dr Kazazian

Jumping genes: a marker for early cancer diagnosis? An interview with Dr Kazazian

Researchers receive NIH grants to find genomic regions containing variants that affect disease risk

Researchers receive NIH grants to find genomic regions containing variants that affect disease risk

Desmoplasmic melanoma may possess unprecedented burden of gene mutations, say UCSF scientists

Desmoplasmic melanoma may possess unprecedented burden of gene mutations, say UCSF scientists

New NIH grants support research that combines DNA sequence information and electronic medical records

New NIH grants support research that combines DNA sequence information and electronic medical records

New study describes multi-method strategy to improve detection of PMS2 gene mutations in Lynch syndrome

New study describes multi-method strategy to improve detection of PMS2 gene mutations in Lynch syndrome

New set of genes can indicate improved survival after surgery for pancreatic cancer patients

New set of genes can indicate improved survival after surgery for pancreatic cancer patients

Researchers uncover genetic circuit involved in obesity

Researchers uncover genetic circuit involved in obesity

Research: Critical aspects of human genome's regulatory program encoded by genomic sequence elements

Research: Critical aspects of human genome's regulatory program encoded by genomic sequence elements

GTEx findings reveal how genomic variants can affect gene activity and disease susceptibility

GTEx findings reveal how genomic variants can affect gene activity and disease susceptibility

Quest Diagnostics to provide whole exome sequencing service to diagnose neurological disorders

Quest Diagnostics to provide whole exome sequencing service to diagnose neurological disorders

Researchers develop quality assurance tool for genome editing

Researchers develop quality assurance tool for genome editing

Genomics of papillary thyroid carcinoma (PTC): an interview with Professor Thomas J. Giordano

Genomics of papillary thyroid carcinoma (PTC): an interview with Professor Thomas J. Giordano

Study: Mutated ATRX gene may serve as much-needed biomarker for rare neuroendocrine tumors

Study: Mutated ATRX gene may serve as much-needed biomarker for rare neuroendocrine tumors

New computational technique reveals genetic roots of autism, cancers

New computational technique reveals genetic roots of autism, cancers

Baylor-led researchers identify gene linked to familial glioma

Baylor-led researchers identify gene linked to familial glioma

Study provides insights into genetic underpinnings of childhood epilepsies

Study provides insights into genetic underpinnings of childhood epilepsies

Researchers discover mitochondrial and nuclear tRNA-lookalikes in human genome

Researchers discover mitochondrial and nuclear tRNA-lookalikes in human genome

Deep sequencing technique opens up new possibilities for finding genetic causes for brain disorder

Deep sequencing technique opens up new possibilities for finding genetic causes for brain disorder

CNIOA researchers update number of human genes to 19,000

CNIOA researchers update number of human genes to 19,000