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New Products: Pathway Genomics' Hereditary Colorectal Test; Courtagen's Epilepsy Test

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Pathway Genomics has launched Hereditary Colorectal Cancer DNA Insight, which uses next-generation sequencing to identify genetic alterations that are indicative of a risk for colorectal cancer, including genes related to Lynch syndrome, familial adenomatous polyposis, Li-Fraumeni syndrome, juvenile polyposis, MUTYH-associated polyposis, Peutz-Jeghers syndrome, hereditary diffuse gastric cancer, and PTEN-hamartoma tumor syndrome.


Courtagen Life Sciences has expanded EpiSeek, its next-generation sequencing test for epilepsy and seizure disorders, to include 489 genes associated with seizure disorders. Additionally, the company has also launched an Infancy and Childhood Epilepsy Panel, which targets 70 genes.

The Scan

Positive Framing of Genetic Studies Can Spark Mistrust Among Underrepresented Groups

Researchers in Human Genetics and Genomics Advances report that how researchers describe genomic studies may alienate potential participants.

Small Study of Gene Editing to Treat Sickle Cell Disease

In a Novartis-sponsored study in the New England Journal of Medicine, researchers found that a CRISPR-Cas9-based treatment targeting promoters of genes encoding fetal hemoglobin could reduce disease symptoms.

Gut Microbiome Changes Appear in Infants Before They Develop Eczema, Study Finds

Researchers report in mSystems that infants experienced an enrichment in Clostridium sensu stricto 1 and Finegoldia and a depletion of Bacteroides before developing eczema.

Acute Myeloid Leukemia Treatment Specificity Enhanced With Stem Cell Editing

A study in Nature suggests epitope editing in donor stem cells prior to bone marrow transplants can stave off toxicity when targeting acute myeloid leukemia with immunotherapy.