The DOI matches its Crossref record; 8 of the 8 references it cites were found in a registry or an index.
Challenges and standards in integrating surveys of structural variation
Open accessAbstract
There has been an explosion of data describing newly recognized structural variants in the human genome. In the flurry of reporting, there has been no standard approach to collecting the data, assessing its quality or describing identified features. This risks becoming a rampant problem, in particular with respect to surveys of copy number variation and their application to disease studies. Here, we consider the challenges in characterizing and documenting genomic structural variants. From this, we derive recommendations for standards to be adopted, with the aim of ensuring the accurate presentation of this form of genetic variation to facilitate ongoing research.
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Self-citationCommon deletion polymorphisms in the human genome
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Self-citationGenome-wide association studies for complex traits: consensus, uncertainty and challenges
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Mapping and sequencing of structural variation from eight human genomes
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Metadata
- Authors
- Scherer, S. W., Lee, C., Birney, E., Altshuler, D. M., Eichler, E. E., Carter, N. P., Hurles, M. E., & Feuk, L.
- Venue
- Nature Genetics
- Published
- 2007-06-27
- Volume
- 39
- Issue
- S7
- Pages
- S7-S15
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W1999674531
- Cited by
- 410
- References
- 8
- FWCI
- 23.95
- Type
- journal article
- Language
- en
- Open access
- green
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