Article

Exome Sequencing reveals characteristic KMT2C mutations in the Indian Phenotype of Cervical Cancer

2022-11-23

Abstract excerpt

We attempted to understand the cervical cancer patient samples through Whole Exome Sequencing. We derived the variants from raw reads via our in-house benchmarked pipeline and validated the variants by IGV. This is the first cervical cancer exome data from the Indian cohort. <h4>Background:</h4> Cervical cancer (CC) is caused mainly by persistent infections of high-risk HPV, reduced parity, and factors like a decr...

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Literature Corpus work: 80134d7b-ea56-59f3-beda-7632a743b118
DOI: 10.20944/preprints202211.0440.v1

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