Next-Generation Sequencing In-Depth Focus 2018
In this In-Depth Focus: hunting mysterious ‘Dark Matter Genome’ towards rewriting the rules of human genetic diseases, and enabling biomarker discovery at single-cell resolution
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In this In-Depth Focus: hunting mysterious ‘Dark Matter Genome’ towards rewriting the rules of human genetic diseases, and enabling biomarker discovery at single-cell resolution
6 September 2018 | By Takara Bio
The data presented in this application note demonstrates how SMARTer ICELL8 Single-Cell System can be used to generate high-quality RNA-seq libraries that provide full-length transcript sequence information from hundreds of single cells in parallel...
In this issue: pharmacological targeting of mitochondrial dysfunction in Parkinson’s disease, the evolving role of three dimensional in-vitro cell culture techniques in drug discovery, and NGS: hunting mysterious ‘Dark Matter Genome’ towards rewriting the rules of genetic diseases.
A new study describes an assay, anchored multiplex PCR (AMP)-based targeted next-generation-sequencing (NGS), with superior diagnostic utility compared to conventional techniques...
The main areas identified to hinder NGS market growth are the lack of skilled professionals and complications relating to data storage...
A first-of-its-kind study implicates another culprit in the path to Alzheimer's disease: the presence of viruses in the brain...
A statistical foundation for Next Generation Sequencing has been built from samples of 1,036 patients...
Target the genes that matter for efficient sequencing and analysis with custom-targeted gene panels.
Researchers have carried out the largest genomic analysis of patients with SMM to explain the biology of the disease and how it unfolds through time...
Biomedical engineers invent an innovative technique to help injured hearts regenerate...
Next generation sequencing (NGS) has transformed biological research, invigorating the field of genomics, and has increased understanding of our genetic basis.
Small non-coding RNAs may be used to devise a diagnostic blood test for pregnant women...
For Thermo Fisher Scientific, 2018 brings with it a suite of new sequencing solutions that continue to promote application flexibility and throughput scalability for oncology, reproductive health, inherited and infectious disease research.
Next generation sequencing sample preparation on the KingFisher platform...
The multiplex and high-throughput capabilities of next-generation sequencing (NGS) allow researchers to study an immense number of DNA/RNA molecules per run, bringing opportunities to study biological or clinical research questions that could not be addressed before...