Article

The use of whole exome sequencing data to identify candidate genes involved in cancer and benign tumour predisposition

2019-01-01

Abstract excerpt

The development of whole exome sequencing has transformed the study of disease predisposition. The sequencing of both large disease sets and smaller rare disease families enables the identification of new predisposition variants and potentially provide clinical insight into disease management. There is no standard protocol for analysing exome sequencing data. Outside of extremely large sequencing studies including...

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Literature Corpus work: a93f87be-b298-561c-8e7e-5880b98fd3b5
DOI: 10.17863/cam.33290

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