Computational methods for discovering structural variation with next-generation sequencing
In the last several years, a number of studies have described large-scale structural variation in several genomes. Traditionally, such methods have used whole-genome array comparative genome hybridization or single-nucleotide polymorphism arrays to detect large regions subject to copy-number variati...
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| Vydáno v: | Nature methods Ročník 6; číslo Suppl 11; s. S13 - S20 |
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| Hlavní autoři: | , , |
| Médium: | Journal Article |
| Jazyk: | angličtina |
| Vydáno: |
New York
Nature Publishing Group US
01.11.2009
Nature Publishing Group |
| Témata: | |
| ISSN: | 1548-7091, 1548-7105, 1548-7105 |
| On-line přístup: | Získat plný text |
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| Shrnutí: | In the last several years, a number of studies have described large-scale structural variation in several genomes. Traditionally, such methods have used whole-genome array comparative genome hybridization or single-nucleotide polymorphism arrays to detect large regions subject to copy-number variation. Later techniques have been based on paired-end mapping of Sanger sequencing data, providing better resolution and accuracy. With the advent of next-generation sequencing, a new generation of methods is being developed to tackle the challenges of short reads, while taking advantage of the high coverage the new sequencing technologies provide. In this survey, we describe these methods, including their strengths and their limitations, and future research directions. |
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| Bibliografie: | ObjectType-Article-1 SourceType-Scholarly Journals-1 content type line 14 ObjectType-Literature Review-2 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 |
| ISSN: | 1548-7091 1548-7105 1548-7105 |
| DOI: | 10.1038/nmeth.1374 |