Recent Publications on complete genomics : |  | |
| Optimized filtering reduces the error rate in detecting genomic variants by short-read sequencing.
Distinguishing single-nucleotide variants (SNVs) from errors in... | 1] Vesalius Research Center, Vlaams Instituut voor Biotechnologie (VIB), | Nat Biotechnol. 2011 Dec 18;30(1):61-8. doi: 10.1038/nbt.2053.
DOI Direct Link |
| Performance comparison of whole-genome sequencing platforms.
Whole-genome sequencing is becoming commonplace, but the accuracy and... | 1] Department of Genetics, Stanford University, Stanford, California, USA. | Nat Biotechnol. 2011 Dec 18;30(1):78-82. doi: 10.1038/nbt.2065.
DOI Direct Link |
| Computational Techniques for Human Genome Resequencing Using Mated Gapped Reads.
Abstract Unchained base reads on self-assembling DNA nanoarrays have... | Complete Genomics Inc. , Mountain View, California. | J Comput Biol. 2011 Dec 16.
DOI Direct Link |
| Company profile: Complete Genomics Inc.
Complete Genomics Inc. is a life sciences company that focuses on complete... | Complete Genomics Inc., 2071 Stierlin Court, Mountain View, CA 94043, USA. | Future Oncol. 2011 Feb;7(2):219-21.
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| Advances in whole genome sequencing technology.
Sanger sequencing revolutionized the field of genetics by becoming the... | Children's Hospital of Philadelphia Research Institute, 34th and Civic | Curr Pharm Biotechnol. 2011 Feb 1;12(2):293-305. |
