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The Genome Sequencer FLX™ System—Longer reads, more applications, straight forward bioinformatics and more complete data sets

Paper ID Volume ID Publish Year Pages File Format Full-Text
24554 43526 2008 8 PDF Available
Title
The Genome Sequencer FLX™ System—Longer reads, more applications, straight forward bioinformatics and more complete data sets
Abstract

The Genome Sequencer FLX System (GS FLX), powered by 454 Sequencing, is a next-generation DNA sequencing technology featuring a unique mix of long reads, exceptional accuracy, and ultra-high throughput. It has been proven to be the most versatile of all currently available next-generation sequencing technologies, supporting many high-profile studies in over seven applications categories. GS FLX users have pursued innovative research in de novo sequencing, re-sequencing of whole genomes and target DNA regions, metagenomics, and RNA analysis. 454 Sequencing is a powerful tool for human genetics research, having recently re-sequenced the genome of an individual human, currently re-sequencing the complete human exome and targeted genomic regions using the NimbleGen sequence capture process, and detected low-frequency somatic mutations linked to cancer.

Keywords
2nd generation sequencing technology; Human re-sequencing; De novo sequencing; Transcriptome analysis; Microbial genome sequencing; Metagenomics; Plants sequencing; Viral variants
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The Genome Sequencer FLX™ System—Longer reads, more applications, straight forward bioinformatics and more complete data sets
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Publisher
Database: Elsevier - ScienceDirect
Journal: Journal of Biotechnology - Volume 136, Issues 1–2, 31 August 2008, Pages 3–10
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Bioengineering
Get Full-Text Now
Don't Miss Today's Special Offer
Price was $35.95
You save - $31
Price after discount Only $4.95
100% Money Back Guarantee
Full-text PDF Download
Online Support
Any Questions? feel free to contact us