Whole exome sequencing of Finnish hereditary breast cancer families

Study ID Alternative Stable ID Type
EGAS00001001835 Other

Study Description

A remarkable proportion of factors causing genetic predisposition to breast cancer (BC) are unknown in non-BRCA1/2 families. Exome sequencing was performed for 13 high-risk Finnish hereditary breast and/or ovarian cancer (HBOC) families to detect variants contributing to BC susceptibility

Study Datasets 1 dataset.

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Dataset ID Description Technology Samples
Dataset contains Whole Exome Sequencing(WES) data from 37 individuals as aligned bam-files. The reads have been aligned using bowtie2 to human genome hg19 build.
Illumina HiSeq 2000 37

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