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RNA_sequencing

All cancers arise due to somatically acquired mutations in their genomes which alter the function of key cancer genes. Understanding the critical mutational events underlying the development of cancer is paramount for advancing prevention, early detection and effective treatment of the disease. Breast cancer is the most common cause of cancer death among women. Extraordinary recent advances in sequencing now make it a realistic aim to sequence large numbers of breast cancer genomes to find somatic mutations on a massive scale. NB bam files for manuscript A_Proteomic_Chronology_of_Gene_Expression_through_the_Cell_Cycle_in_Human_Myeloid_Leukemia_Cells are now available at the following link:http://www.ebi.ac.uk/ena/data/view/ERP008483

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
EGAD00001000285 Illumina Genome Analyzer II Illumina HiSeq 2000 55
EGAD00001001019 Illumina HiSeq 2000 1
EGAD00001002236 Illumina Genome Analyzer II Illumina HiSeq 2000 32
Publications Citations
Direct Transcriptional Consequences of Somatic Mutation in Breast Cancer.
Cell Rep 16: 2016 2032-2046
27