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tag whole genome sequencing genetics genomics disease medicine cell molecular biology

Explore How Multiomics Offers a More Holistic View of Biology for Disease Research
Powering Discovery with Multiomics
Illumina | Jun 8, 2023 | 1 min read
Multiomics combines multiple layers of biology to power new discoveries in disease research. 
DNA molecule.
Finding DNA Tags in AAV Stacks
Mariella Bodemeier Loayza Careaga, PhD | Mar 7, 2024 | 8 min read
Ten years ago, scientists put DNA barcodes in AAV vectors, creating an approach that simplified, expedited, and streamlined AAV screening. 
Unlocking the Secrets within Cells Using Next Generation Sequencing
Unlocking the Secrets within Cells Using Next Generation Sequencing 
The Scientist | Sep 25, 2023 | 1 min read
Next generation sequencing (NGS) core facility scientists and researchers discuss their latest work exploring novel cancer models and stem cells in space.
TSS
Genomes Across the Tree of Life
The Scientist | Mar 23, 2023 | 2 min read
Researchers turn to unique eukaryotes to better understand how DNA is organized in 3D space.
A reticulated giraffe in Samburu National Park, Kenya
Whole-Genome Data Point to Four Species of Giraffe
Ruth Williams | May 6, 2021 | 4 min read
The genome sequences of 51 giraffes from all over Africa contribute to the latest attempt in an ongoing pursuit to pin down a species number.
Glowing red DNA on bluish background
Redesigning Medicine Using Synthetic Biology
Alison Halliday, PhD, Technology Networks | Jun 21, 2023 | 5 min read
Drawing inspiration from nature, synthetic biology offers exciting opportunities to transform the future of medicine.
New Strategies to Discover Human Disease Genes
New Strategies to Discover Human Disease Genes
The Scientist | Oct 16, 2023 | 2 min read
Learn how researchers across health-related fields identify and characterize disease-causing genomic variants.
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
Blue-toned illustration of the DNA double helix, with additional DNA strands in the background
Nearly Complete Human Genome Sequenced
Jef Akst | Jun 8, 2021 | 2 min read
In a preprint, researchers fill in some of the holes left in the first draft of the human genetic code, published at the turn of the century.
Infusion of Artificial Intelligence in Biology
Meenakshi Prabhune, PhD | Feb 23, 2024 | 10 min read
With deep learning methods revolutionizing life sciences, researchers bet on de novo proteins and cell mapping models to deliver customized precision medicines.

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