Solexa Whole Genome Paired End Analysis
| Summary |
A paired-end sequencing approach using Illumina massively parallel
sequencing has been used to characterise structural variants in two
Lung Cancer Cell Lines.
Reference:
Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing.
Campbell PJ, et al.
Nat Genet. 2008 Jun;40(6):722-9. Epub 2008 Apr 27. PMID: 18438408
Please visit the CGP Trace Archive for the raw ztr and fastq data files for this study.
|
|
Lung Rearrangement Screens:
|
| | Samples | 2 | |
| | COSMIC Point Mutations | 241 | |
| | Structural Variants | 40 | |
| | Observed Breakpoints | 103 | |
|
|