How Can Diverse Genomic Approaches Improve Rare Disease Research?
Tomi Pastinen, MD, PhD
Multiomic techniques can robustly screen and identify often-missed genetic determinants of rare diseases
omics
Spatial-Omics Technology Enables Investigation of Diseases at Early Stages
Helmholtz Zentrum München
New technology uses robotics to obtain proteomics data from diseased cells early on
Genes to Potentially Diagnose Long-Term Lyme Disease Identified
Mount Sinai School of Medicine
Findings could lead to new diagnostics and treatments for the hard-to-detect condition
Mayo Study Lays Foundation to Predict Antidepressant Response
Mayo Clinic
Researchers identify biomarkers that correlate with response to antidepressant treatment
Genetic Diversity in the Aging Human Brain
Zahraa Chorghay, PhD
Structural variants provide clues to cell function and disease in the brain
Solving Rare Disease Mysteries with Genomics
Brydie Thomas-Moore, PhD
The Solve-RD consortium is striving to improve rare disease diagnostics using genomics
“Lights Out Science” Will Transform Precision Medicine
Aaron Hudson, PhD
A fully automated approach to -omics analysis is improving outcomes for a range of diseases
The Power of Multi-Omics at the Single-Cell Level
Today's Clinical Lab
How researchers are leveraging technology to gather multiple layers of data on individual cells