ADVERTISEMENT

404

Not Found

Is this what you were looking for?

tag coronary heart disease genetics genomics

Layered visual representation of multiomics
Integrate and Innovate with NGS and Multiomics
The Scientist and Illumina | May 4, 2023 | 6 min read
Researchers across disciplines combine layers of discovery obtained with accessible NGS-based multiomics approaches.
Researchers in George Church&rsquo;s lab modified wild type ADK proteins (left) in <em >E.coli</em>, furnishing them with an nonstandard amino acid (nsAA) meant to biocontain the resulting bacterial strain.
A Pioneer of The Multiplex Frontier
Rashmi Shivni, Drug Discovery News | May 20, 2023 | 10 min read
George Church is at it again, this time using multiplex gene editing to create virus-proof cells, improve organ transplant success, and protect elephants.
Genome Collector: A Profile of Charles Rotimi
Anna Azvolinsky | Oct 1, 2018 | 9 min read
The NIH epidemiologist has worked to ensure genetic health and population genetics studies contain data from African—not just European—populations.
Rare History, Common Disease
David Secko | Jul 1, 2008 | 10 min read
Rare History, Common Disease A unique population in Quebec is helping reveal the genetics behind common diseases such as heart disease and asthma. But as it loses its isolation, is time running out? By David Secko Related Articles 1 The novel loci include regions that contain novel candidate Crohn disease genes such as JAKMIP1, which is involved in interleukin-23 signaling, and LOC285484, which is similar to a secreted cytokine potentially involved in
polygenic risk score genetics genomics direct to consumer genome sequencing gwas
Researchers Develop Standards for Reporting Polygenic Risk Scores
Marcus A. Banks | Mar 17, 2021 | 3 min read
Current reporting about the contribution of genetic variations to a person’s risk of disease is often incomplete and hard to interpret, according to the authors of a set of best practices for presenting such information.
The dark matter of disease
Hannah Waters | Apr 24, 2011 | 5 min read
Scientists are beginning to unravel how non-coding DNA works across long distances of the genome to influence disease
Techniques for Assessing Genomic Copy Number Variations
Sarah C.P. Williams | Oct 1, 2016 | 8 min read
As the importance of genomic copy number variations for health and disease becomes clearer, researchers are creating new ways to detect these changes in the genome.
Macrophages Are the Ultimate Multitaskers
Claire Asher | Oct 1, 2017 | 10+ min read
From guiding branching neurons in the developing brain to maintaining a healthy heartbeat, there seems to be no job that the immune cells can’t tackle.
Whole-Genome SNP Genotyping
Marilee Ogren | Jun 1, 2003 | 8 min read
Clockwise from top left: images courtesy of Affymetrix, Illumina, Sequenom and Illumina Take any two individuals, sequence and compare their genomic DNA, and you'll find that the vast majority (about 99.9%) of the sequences are identical. In the remaining 0.1% lie differences in disease susceptibility, environmental response, and drug metabolism. Researchers are understandably keen to dissect these variations, most of which take the form of single-nucleotide polymorphisms (SNPs). A SNP (pron
A Genomics Payoff?
Aaron J. Bouchie | Apr 1, 2006 | 5 min read
Is diagnostics the best bet for companies such as Celera that once put its money on drug development?

Run a Search

ADVERTISEMENT