Clues taken from small molecules in saliva may be able to help diagnose and predict the duration of concussions in children.
Diagnostics allow for the identification of cancer types and other crucial biomarkers, and are used right through from discovery to market.
A genome-wide association study has identified 4 novel SNPs that may be able to act as prognostic tools for early-onset breast cancer in young women
PCR-based approach to a frontier of the human genome could speed discovery in chromosome-based diseases and birth defects.
A study explains that one fifth of patients with cancer experienced post-traumatic stress disorder (PTSD) several months after diagnosis.
It has been reported that some people have two different sets of DNA, and if they do, they are known as human chimeras. This can happen a number of ways.
Bionano Genome Mapping found to be superior to existing clinical tests for the identification of pathogenic structural variants in DMD.
ACMG is developing a series of one-page documents to help guide doctors through discussing incidental findings and NIPT results with patients
CBSN has reported on the successes of the NIH’s BabySeq Project and some of the privacy and discrimination concerns parents have voiced about sequencing their children
ASHG 2017: Edico Genome & Fabric Genomics to provide an integrated solution for secondary and tertiary analysis of next-generation sequencing data.
Genomic Vision has granted AmCare Genomics Laboratory exclusive rights to market their FSHD diagnostic assay in China
Expanded Potential Stem Cells have been created, that, for the first time, can produce all three types of blastocyst stem cells: embryo, placenta & yolk sac.
Genetics account for as much as four out of five cases of schizophrenia according to new research.
New research into improving the genetic decoding of neurodevelopmental disorders promises to help future diagnosis of children with such conditions.