First, the team searched for variants in just a single letter of the DNA code, called single nucleotide polymorphisms (SNPs), ...

Researchers conducted a study to determine if variations in the MTNR1A gene, specifically the MRNR1A variant (rs374152717), could be a genetic cause of idiopathic osteoporosis.

A collaborative study by researchers from Baylor College of Medicine and Illumina has showcased the exceptional capabilities of the DRAGEN (Dynamic Read Analysis for GENomics) platform in ...

Whole genome sequence data were obtained from the TOPMed Freeze 9 dataset, which consists of over 160,000 samples and approximately 800 million single nucleotide variants. Only variants with at ...

Caris said MI Cancer Seek will be used as a companion diagnostic to identify cancer patients who may benefit from treatment ...

The frequency of variant alleles for drug-metabolizing ... We have focused on the most common single nucleotide polymorphisms (SNPs), the inherited nature of their deficiency, their frequency ...

Recent technological advances have enabled genome-wide single nucleotide polymorphism (SNP) association testing and copy number variant (CNV) identification. Several CNV loci have been identified ...

In her portion of the presentation, Dr. Felton will highlight recent advances in using long-read RNA sequencing to detect ...

MI Cancer Seek is a next-generation sequencing (NGS) based in vitro diagnostic (IVD) device using total nucleic acid (TNA) ...

AX-0810 targeting NTCP for cholestatic diseases to be first ProQR Axiomer™ RNA editing program to enter the clinic Company to host virtual ...