ENAapplication/xmlprimaryOK2000000GenomicsWASHINGTON UNIVERSITYhttps://www.ebi.ac.uk/ena/browser/view/PRJNA74805Homo sapiensBreast Cancer Subject Participant ID 700064 (Source Sample names: 6888 and 206). We used massively parallel DNA sequencing technologies to screen entire genomes, in an unbiased manner, for genetic changes associated with tumor growth and metastasis. We describe the complete genome sequence analysis of four DNA samples from a 44-year old African-American patient with basal-like breast cancer: peripheral blood, the primary tumor, a brain metastasis that developed within a year of initial therapy, and a first-passage xenograft derived from the primary tumor. A total of 50 validated mutations were discovered within coding, RNA, or splice site sequences. Of these, 20 mutations were abundantly present in all three tumors, including mutations in CSMD1 and JAK2. These two genes subsequently were found to be mutated in other breast tumors. The metastasis contained two de novo mutations not present in the primary tumor, and was significantly enriched for 20 shared... (for more see dbGaP study page.)ENABC, Complete, Complete Genome, Whole Genome, breast cancer, breast., cancer of breast, Whole, carcinoma of breast, Complete Genome Sequencing, Genome Sequencing, NOS, cancer of the breast, breast carcinoma, mammary carcinoma, carcinoma of the breast, cancer, Sequencinghuman being, human., man00.00.00.00.00.0falseHomo sapiensWhole Genome Sequencing of Triple Negative Breast Cancer2022-05-122013-06-27PRJNA74805203935559606