High-throughput sequencing technologies
The human genome sequence has profoundly altered our understanding of biology, human diversity, and disease. The path from the first draft sequence to our nascent era of personal genomes and genomic medicine has been made possible only because of the extraordinary advancements in DNA sequencing tech...
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| Veröffentlicht in: | Molecular cell Jg. 58; H. 4; S. 586 |
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| Hauptverfasser: | , , |
| Format: | Journal Article |
| Sprache: | Englisch |
| Veröffentlicht: |
United States
21.05.2015
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| ISSN: | 1097-4164, 1097-4164 |
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| Abstract | The human genome sequence has profoundly altered our understanding of biology, human diversity, and disease. The path from the first draft sequence to our nascent era of personal genomes and genomic medicine has been made possible only because of the extraordinary advancements in DNA sequencing technologies over the past 10 years. Here, we discuss commonly used high-throughput sequencing platforms, the growing array of sequencing assays developed around them, as well as the challenges facing current sequencing platforms and their clinical application. |
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| AbstractList | The human genome sequence has profoundly altered our understanding of biology, human diversity, and disease. The path from the first draft sequence to our nascent era of personal genomes and genomic medicine has been made possible only because of the extraordinary advancements in DNA sequencing technologies over the past 10 years. Here, we discuss commonly used high-throughput sequencing platforms, the growing array of sequencing assays developed around them, as well as the challenges facing current sequencing platforms and their clinical application. The human genome sequence has profoundly altered our understanding of biology, human diversity, and disease. The path from the first draft sequence to our nascent era of personal genomes and genomic medicine has been made possible only because of the extraordinary advancements in DNA sequencing technologies over the past 10 years. Here, we discuss commonly used high-throughput sequencing platforms, the growing array of sequencing assays developed around them, as well as the challenges facing current sequencing platforms and their clinical application.The human genome sequence has profoundly altered our understanding of biology, human diversity, and disease. The path from the first draft sequence to our nascent era of personal genomes and genomic medicine has been made possible only because of the extraordinary advancements in DNA sequencing technologies over the past 10 years. Here, we discuss commonly used high-throughput sequencing platforms, the growing array of sequencing assays developed around them, as well as the challenges facing current sequencing platforms and their clinical application. |
| Author | Reuter, Jason A Spacek, Damek V Snyder, Michael P |
| Author_xml | – sequence: 1 givenname: Jason A surname: Reuter fullname: Reuter, Jason A organization: Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA – sequence: 2 givenname: Damek V surname: Spacek fullname: Spacek, Damek V organization: Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA – sequence: 3 givenname: Michael P surname: Snyder fullname: Snyder, Michael P email: mpsnyder@stanford.edu organization: Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA. Electronic address: mpsnyder@stanford.edu |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26000844$$D View this record in MEDLINE/PubMed |
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| PublicationPlace | United States |
| PublicationPlace_xml | – name: United States |
| PublicationTitle | Molecular cell |
| PublicationTitleAlternate | Mol Cell |
| PublicationYear | 2015 |
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| Title | High-throughput sequencing technologies |
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