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Exome Sequencing of Poor Prognosis Acute Myeloid Leukaemia (2019-08-19)

We plan to sequence the exomes of 4 AML cases (tumour and germline) in an effort to discover new mutations in this disease that could improve our understanding of leukaemogenesis and guide the development of new targeted therapies. The Sanger Institute will sequence the exomes of 4 Acute Myeloid Leukaemia cases including tumour and germline DNA so that somatically-acquired, AML-specific mutations can be accurately designated. . This dataset contains all the data available for this study on 2019-08-19.

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Wellcome Trust Sanger Institute Data Sharing Policy

Studies are experimental investigations of a particular phenomenon, e.g., case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients.

Study ID Study Title Study Type
EGAS00001000146 Other

This table displays only public information pertaining to the files in the dataset. If you wish to access this dataset, please submit a request. If you already have access to these data files, please consult the download documentation.

ID File Type Size Located in
EGAF00000112969 bam 9.5 GB
EGAF00000112970 bam 9.3 GB
EGAF00000144684 bam 4.0 GB
EGAF00000144685 bam 4.6 GB
EGAF00000144686 bam 4.2 GB
EGAF00000172184 bam 5.6 GB
EGAF00000172185 bam 1.2 GB
EGAF00000172186 bam 4.6 GB
EGAF00000172187 bam 3.3 GB
9 Files (46.2 GB)