Karolinska Institute
Whole-Genome Sequencing Aids Rare Disease Diagnosis in Stockholm-Area Healthcare System
In the first five years of the Genomic Medicine Center Karolinska-Rare Disease program, molecular diagnoses were generated for about 40 percent of patients.
Neanderthal-Origin Haplotype Provides Protection Against Severe COVID-19
The same researchers previously found a different Neanderthal-origin haplotype increased COVID-19 risk, highlighting their complex influence on humans.
The new plate-based protocol developed at the Karolinska Institute combines low-coverage WGS and SMART-Seq2 transcriptomics for single-cells.
Years of Regular Endurance Exercise Leads to Transcriptomic Shifts in Muscles, Study Finds
Sex differences in muscle gene expression were further reduced with long-term endurance exercise, an international research team found.
Illumina, Genomic Medicine Sweden to Evaluate Sequencing-Based Leukemia Diagnostics
The study will compare whole-genome sequencing and RNA sequencing to conventional diagnostic methods in about 450 acute leukemia patients in Sweden.
Mar 19, 2020
Dec 3, 2019
Apr 2, 2019