PANETs - RNA-seq, Exome & Genome

Exome, targetted-capture, RNA and shallow whole-genome sequencing of pancreatic neuroendocrine tumours

Description: This dataset includes 51 samples from 19 individuals with pancreatic neuroendocrine tumours. These samples were analyzed using RNA-sequencing, whole-exome sequencing, shallow (~0.3x) whole-genome sequencing, and a 21-gene panel targeted capture sequencing. Everything was sequenced using the Illumina HiSeq and is provided in BAM or FASTQ format.
Authors: Rene Quevedo, Anna Spreafico, Jeff Bruce, Arnavaz Danesh, Samah El Ghamrasni, Amanda Giesler, Youstina Hanna, Cherry Have, Tiantian Li, S. Y. Cindy Yang, Tong Zhang, Sylvia L. Asa, Benjamin Haibe-Kains, Monika Krzyzanowska, Adam C. Smith, Simron Singh, Lillian L. Siu & Trevor J. Pugh
Lab: Pugh
Year: 2020
Keywords: Pancreatic neuroendocrine tumor, copy-neutral, loss of heterozygosity, aneuploidy


Quevedo, R., Spreafico, A., Bruce, J. et al. Centromeric cohesion failure invokes a conserved choreography of chromosomal mis-segregations in pancreatic neuroendocrine tumor. Genome Med 12, 38 (2020).

51 samples

Sample Type:Pancreatic
Datatype:Sequencing BAMs and FASTQs
Technology:RNA-seq, Exome, Genome


This dataset is available by request only.

Contact: Carl Virtanen

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