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The diagnostic application of RNA sequencing in patients with thyroid cancer: An analysis of 851 variants and 133 fusions in 524 genes

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The diagnostic application of RNA sequencing in patients with thyroid cancer: An analysis of 851 variants and 133 fusions in 524 genes

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Thyroid carcinomas are known to harbor oncogenic driver mutations and advances in sequencing technology now allow the detection of these in fine needle aspiration biopsies (FNA). Recent work by The Cancer Genome Atlas (TCGA) Research Network has expanded the number of genetic alterations detected in papillary thyroid carcinomas (PTC).

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Nội dung Text: The diagnostic application of RNA sequencing in patients with thyroid cancer: An analysis of 851 variants and 133 fusions in 524 genes

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