HNO Team Data Access Committee

Simon S Laban
simon.laban@uniklinik-ulm.de

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Dataset ID	Description	Technology	Samples
EGAD00001009167	This dataset comprises genetic variation data (as somatic indels and snvs VCFs) of 38 OPSCC tumors. WES was done using NextSeq 500 System running in 150 cycles (2x 75bp paired-end) mode. Sequence information was converted to FASTQ format using bcl2fastq v2.20.0.422. VCFs were generated using the Strelka package.		1