Methodology article
CNV-seq, a new method to detect copy number variation using high-throughput sequencing
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* Corresponding author: Martti T Tammi martti.tammi@ki.se
1 Department of Biological Sciences, National University of Singapore, Singapore
2 Department of Biochemistry, National University of Singapore, Singapore
3 Karolinska Institutet, Department of Microbiology, Tumor and Cell Biology, Stockholm, Sweden
BMC Bioinformatics 2009, 10:80 doi:10.1186/1471-2105-10-80
Published: 6 March 2009Additional files
Additional File 1:
CNV regions identified between Venter's and Watson's genomes. The 174 identified CNV regions, including the length, location, log2 ratio, and p-value for each of the regions.
Format: TXT Size: 10KB Download file
