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Cancer and genomics
被引:0
|作者:
P. Andrew Futreal
Arek Kasprzyk
Ewan Birney
James C. Mullikin
Richard Wooster
Michael R. Stratton
机构:
[1] Cancer Genome Project and,
[2] Informatics Division,undefined
[3] Sanger Centre,undefined
[4] Wellcome Trust Genome Campus,undefined
[5] EBI-EMBL,undefined
[6] Wellcome Trust Genome Campus,undefined
[7] Institute of Cancer Research,undefined
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摘要:
Identification of the genes that cause oncogenesis is a central aim of cancer research. We searched the proteins predicted from the draft human genome sequence for paralogues of known tumour suppressor genes, but no novel genes were identified. We then assessed whether it was possible to search directly for oncogenic sequence changes in cancer cells by comparing cancer genome sequences against the draft genome. Apparently chimaeric transcripts (from oncogenic fusion genes generated by chromosomal translocations, the ends of which mapped to different genomic locations) were detected to the same degree in both normal and neoplastic tissues, indicating a significant level of false positives. Our experiment underscores the limited amount and variable quality of DNA sequence from cancer cells that is currently available.
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页码:850 / 852
页数:2
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