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SNP data from 125 hepatocellular carcinomas and 112 paired normal samples

GSE32649 Homo sapiens Genome variation profiling by SNP array 237 samples Submitted 2012/02/27 Platform GPL6986Platform GPL13135
Summary
SNP array data from 125 hepatocellular carcinomas were used to detect recurrent copy number alterations.
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Direct links to NCBI, no account and no request form: the whole study as GSE32649_RAW.tar, processed values as the series matrix, the supplementary file directory, and per-sample supplementary files for any of the 237 samples.

Also filed as BioProject PRJNA146959. Searching any of these in the dataset finder brings you back here.

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