Name
Abstract | ||
|---|---|---|
Massively parallel sequencing technologies continue to alter the study of human genetics. As the cost of sequencing declines, next-generation sequencing (NGS) instruments and datasets will become increasingly accessible to the wider research community. Investigators are understandably eager to harness the power of these new technologies. Sequencing human genomes on these platforms, however, presents numerous production and bioinformatics challenges. Production issues like sample contamination, library chimaeras and variable run quality have become increasingly problematic in the transition from technology development lab to production floor. Analysis of NGS data, too, remains challenging, particularly given the short-read lengths (35-250 bp) and sheer volume of data. The development of streamlined, highly automated pipelines for data analysis is critical for transition from technology adoption to accelerated research and publication. This review aims to describe the state of current NGS technologies, as well as the strategies that enable NGS users to characterize the full spectrum of DNA sequence variation in humans. |
Year | DOI | Venue |
|---|---|---|
2010 | 10.1093/bib/bbq016 | BRIEFINGS IN BIOINFORMATICS |
Keywords | Field | DocType |
massively parallel sequencing,next generation sequencing,human genome,variant detection,short read alignment,whole genome sequencing | Technology development,Genome,Human genetics,Massive parallel sequencing,Biology,Whole genome sequencing,Emerging technologies,DNA sequencing,Bioinformatics,Human genome | Journal |
Volume | Issue | ISSN |
11 | SP5 | 1467-5463 |
Citations | PageRank | References |
18 | 1.47 | 13 |
Authors | ||
4 | ||
Name | Order | Citations | PageRank |
|---|---|---|---|
| Daniel C. Koboldt | 1 | 125 | 12.00 |
| Li Ding | 2 | 160 | 25.53 |
| Elaine R. Mardis | 3 | 239 | 23.34 |
| Richard K. Wilson | 4 | 228 | 18.84 |