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Genome-wide genetic marker discovery and genotyping using next-generation sequencing

期刊

NATURE REVIEWS GENETICS
卷 12, 期 7, 页码 499-510

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/nrg3012

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资金

  1. UK Natural Environment Research Council [NE/H019804/1]
  2. US National Institutes of Health (NIH) [1R24GM079486-01A1]
  3. US National Science Foundation [IOS-0843392]
  4. Keck Foundation
  5. NIH National Research Service [1F32GM095213-01]
  6. US National Human Genome Research Institute [R21HG003834, R21HG006036]
  7. BBSRC [BB/G00661X/1, BB/F021135/1, BB/H023844/1] Funding Source: UKRI
  8. MRC [G0900740] Funding Source: UKRI
  9. NERC [NE/H019804/1, NBAF010003] Funding Source: UKRI
  10. Biotechnology and Biological Sciences Research Council [BB/F021135/1, BB/H023844/1, BB/G00661X/1] Funding Source: researchfish
  11. Medical Research Council [G0900740] Funding Source: researchfish
  12. Natural Environment Research Council [NBAF010003, NE/H019804/1] Funding Source: researchfish

向作者/读者索取更多资源

The advent of next-generation sequencing (NGS) has revolutionized genomic and transcriptomic approaches to biology. These new sequencing tools are also valuable for the discovery, validation and assessment of genetic markers in populations. Here we review and discuss best practices for several NGS methods for genome-wide genetic marker development and genotyping that use restriction enzyme digestion of target genomes to reduce the complexity of the target. These new methods-which include reduced-representation sequencing using reduced-representation libraries (RRLs) or complexity reduction of polymorphic sequences (CRoPS), restriction-site-associated DNA sequencing (RAD-seq) and low coverage genotyping-are applicable to both model organisms with high-quality reference genome sequences and, excitingly, to non-model species with no existing genomic data.

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