Difference between revisions of "Next Generation Sequencing"
imported>Sanzhar Aitbay (Created page with "<p><img alt="" src="/ckfinder/userfiles/images/Picture1(1).png" style="height:220px; width:400px" /></p> <p style="margin-left: 40px;">This Review focuses on commercially availa...") |
imported>Sanzhar Aitbay |
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<p><img alt="" src="/ckfinder/userfiles/images/Picture1(1).png" style="height:220px; width:400px" /></p> | <p><img alt="" src="/ckfinder/userfiles/images/Picture1(1).png" style="height:220px; width:400px" /></p> | ||
| − | <p style="margin-left: 40px | + | <p style="margin-left:40px">This Review focuses on commercially available technologies from<strong> Roche/454, Illumina/Solexa, Life/APG and Helicos BioSciences, the Polonator instrument </strong>and the near-term technology of<strong> Pacific Biosciences, </strong></p> |
| − | <p style="margin-left: 40px | + | <p style="margin-left:40px">Here, I present a technical review of<strong> template preparation, sequencing and imaging, genome alignment and assembly</strong>, and current NGS platform performance to provide guidance on <em>how these technologies work and how they may be applied to important biological questions. </em></p> |
| − | these technologies work and how they may be applied | ||
| − | to important biological questions. </p> | ||
| − | <p style="margin-left: 40px;"> | + | <p style="margin-left:40px"><img alt="" src="/ckfinder/userfiles/images/Picture2(1).png" style="height:13px; width:200px" /></p> |
| − | <p style="margin-left: | + | <p style="margin-left: 80px;">Sequencing technologies include a number of methods<br /> |
| + | that are grouped broadly as <strong>template preparation,<br /> | ||
| + | sequencing and imaging, and data analysis.</strong></p> | ||
| − | <p style="margin-left: | + | <ul> |
| + | <li style="margin-left: 80px;"> | ||
| + | <p><em>There are two methods used in preparing templates for NGS reactions</em>: <strong>clonally amplified templates</strong> originating from single DNA molecules, and<strong> single DNA molecule templates</strong></p> | ||
| + | </li> | ||
| + | <li style="margin-left: 80px;"> | ||
| + | <p><em>Sequencing methods are classified as</em> <strong>cyclic reversible termination (CRT), single-nucleotide addition (SNA) and real-time sequencing.</strong> </p> | ||
| + | </li> | ||
| + | </ul> | ||
| − | <p | + | <p> </p> |
| − | <p style="margin-left: 40px;"> </p> | + | <p style="margin-left:40px"> </p> |
| + | |||
| + | <p style="margin-left:40px"> </p> | ||
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| + | <p style="margin-left:40px"> </p> | ||
Revision as of 16:36, 9 December 2017
This Review focuses on commercially available technologies from Roche/454, Illumina/Solexa, Life/APG and Helicos BioSciences, the Polonator instrument and the near-term technology of Pacific Biosciences,
Here, I present a technical review of template preparation, sequencing and imaging, genome alignment and assembly, and current NGS platform performance to provide guidance on how these technologies work and how they may be applied to important biological questions.
Sequencing technologies include a number of methods
that are grouped broadly as template preparation,
sequencing and imaging, and data analysis.
-
There are two methods used in preparing templates for NGS reactions: clonally amplified templates originating from single DNA molecules, and single DNA molecule templates
-
Sequencing methods are classified as cyclic reversible termination (CRT), single-nucleotide addition (SNA) and real-time sequencing.
