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Next-Generation Sequencing

2016
Endometrial cancers are the most frequently diagnosed gynecological malignancy and were expected to be the seventh leading cause of cancer death among American women in 2015. The majority of endometrial cancers are of serous or endometrioid histology. Most human tumors, including endometrial tumors, are driven by the acquisition of pathogenic mutations
Matthieu, Le Gallo   +2 more
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Next-generation DNA sequencing

Nature Biotechnology, 2008
DNA sequence represents a single format onto which a broad range of biological phenomena can be projected for high-throughput data collection. Over the past three years, massively parallel DNA sequencing platforms have become widely available, reducing the cost of DNA sequencing by over two orders of magnitude, and democratizing the field by putting ...
Jay, Shendure, Hanlee, Ji
openaire   +2 more sources

Regulation of Next Generation Sequencing

Journal of Law, Medicine & Ethics, 2014
Since the first draft of the human genome was published in 2001, DNA sequencing technology has advanced at a remarkable pace. Launched in 1990, the Human Genome Project sought to sequence all three billion base pairs of the haploid human genome, an endeavor that took more than a decade and cost nearly three billion dollars.
Gail H, Javitt, Katherine Strong, Carner
openaire   +2 more sources

Next-generation sequencing in the clinic

Nature Biotechnology, 2013
Pools of cell lines carrying a variety of known mutations are used to validate the performance of a cancer diagnostic test based on next-generation sequencing.
Jason Y. Park   +2 more
openaire   +3 more sources

Next generation sequencing technologies

Drug Discovery Today: Technologies, 2005
From the investigation of disease-associated loci in humans, to monitoring the changing genomes of pathogenic viruses and bacteria, sequencing is a powerful and versatile tool. A new generation of sequencing technologies will increase the speed and lower the cost of sequencing, and promises to expand the utility of sequencing in drug discovery and ...
openaire   +2 more sources

[Next Generation Sequencing and ADPKD].

Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia, 2015
Autosomal Dominant Polycistic Kidney Disease (ADPKD) is the most common inherited genetic disorder in the word, caused by mutations in PKD1 gene in 85% of cases and PKD 2 gene in the remaining 15%. Although diagnosis is usually based on ultrasound, MRI and CT scans, in some cases genetic testing is necessary, for example, in patients with atypical ...
Restivo, Arianna   +6 more
openaire   +4 more sources

Next-Generation Sequencing Platforms

Annual Review of Analytical Chemistry, 2013
Automated DNA sequencing instruments embody an elegant interplay among chemistry, engineering, software, and molecular biology and have built upon Sanger's founding discovery of dideoxynucleotide sequencing to perform once-unfathomable tasks. Combined with innovative physical mapping approaches that helped to establish long-range relationships between
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Sequencing the next generation of glioblastomas

Critical Reviews in Clinical Laboratory Sciences, 2018
The most aggressive brain malignancy, glioblastoma, accounts for 60-70% of all gliomas and is uniformly fatal. According to the molecular signature, glioblastoma is divided into four subtypes (proneural, neural, classical, and mesenchymal), each with its own genetic background.
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Next-Generation Sequencing

Current Pharmaceutical Design, 2019
Background: With the outbreak of high throughput next-generation sequencing (NGS), the biological research of drug discovery has been directed towards the oncology and infectious disease therapeutic areas, with extensive use in biopharmaceutical development and vaccine production.Method: In this review, an effort was made to address the basic ...
Tripathi, Pooja   +3 more
openaire   +2 more sources

Next-generation sequencing-by-hybridization

Nature Biotechnology, 2008
A new hybridization-based technology offers advantages in sequencing genomes for which a reference genome exists.
openaire   +2 more sources

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