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ena-DATASET-UH-tumorgenomics-02-04-2019-10:42:45:666-263 - samples

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The data consists of 47 exome-sequenced synchronous colorectal cancers from 23 patients. The exomes of corresponding normal samples were used to remove germline variants. All patients are Finnish (white Caucasian). All except one patient (sync_11 who belongs to a LS family) were assumed sporadic. The sequence data was produced with Illumina HiSeq 4000.EGA dataset EGAD00001004884

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2019-04-08
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