Whole Genome Sequencing by Ion Torrent Next-Generation Sequencing
Whole genome sequencing is used to read the complete DNA sequence of an organism. It has been applied to a wide range of scientific questions, such as those related to the study of inherited diseases, cancer, infectious diseases, prenatal genetics, and much more. Ion Torrent™ next-generation sequencing is ideal for whole genome sequencing of species of various sizes and complexities.
The evolution of fast, affordable whole genome sequencing of microbes has been critical for facilitating a rapid response during disease surveillance, for investigating disease outbreaks, and for determining disease etiology. The power of Ion Torrent™ next-generation sequencing can be used to discriminate between closely related strains and to track the evolution of disease-associated isolates in real time, offering the possibility of incredibly fast identification of outbreak strains.
Researchers focusing on detecting aneuploidy—abnormal chromosome numbers—can use the Ion PGM™ System with whole genome amplification from a single cell and low-pass copy number analysis with Ion Reporter™ Software. This application is faster than microarray or karyotyping analysis and enables multiplexing of samples, offering researchers a flexible and less expensive platform that can deliver accurate data in a single day.
Human-Scale Deep Genome Sequencing
Whole genome sequencing has also been used to uncover the role of de novo mutations in sporadic and inherited diseases, to provide insights into the complexity of cancer, and to identify new genes and biological pathways implicated in tumor initiation, progression, and metastasis. Whole genome sequencing has also provided a glimpse into our planet's genetic past—for example, by uncovering the genome sequences of extinct species such as Neanderthal man and the woolly mammoth. Fast, affordable human-scale genome sequencing using Ion Torrent™ semiconductor technology will help accelerate the application of whole genome sequencing to many additional scientific questions.
For Research Use Only. Not for use in diagnostic procedures.
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