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BGISEQ-500 Cancer Dataset - WGS tumour/normal pairs

This study contains whole genome sequencing data for 3 matched tumour / normal pairs from Mesothelioma patients. The sequencing is 50bp paired-end generated using the BGISEQ-500 and is provided as 6 aligned and duplicate-marked BAM files.

Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data

Dataset ID Description Technology Samples
EGAD00001003221 6
Publications Citations
Germline and somatic variant identification using BGISEQ-500 and HiSeq X Ten whole genome sequencing.
PLoS One 13: 2018 e0190264
Genomics and Epigenetics of Malignant Mesothelioma.
High Throughput 7: 2018 E20