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Single cell whole genome sequencing of 5 ovarian cancer specimens

Single cell whole genome sequencing BAM files for five ovarian cancer specimens.

1 Dataset 1 Publication

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
EGAD50000002102	Five primary, treatment-naive ovarian cancer specimens were subjected to single cell whole genome sequencing (10x Genomics workflow). Libraries were sequenced on an Illumina NovaSeq 6000 instrument. Sequencing data was processed with the Cell Ranger DNA pipelines. Archived here are BAM files for each sample.	Illumina NovaSeq 6000	5

Publications	Citations
Integrated Single-Cell Whole-Genome Sequencing and Spatial Transcriptomics Reveal Intratumoral Heterogeneity in Ovarian Cancer. Bassiouni R, Jin Y, Gibbs LD, Qian J, Rotimi SO, Miller H, Webb MG, Rajpara S, Arias-Stella J, Craig DW, Roman L, Carpten JD. Cancer Res Commun 6: 2026 1020-1035	0