Study
2017 prospective v2 Whole Exome Sequencing
| Study ID | Alternative Stable ID | Type |
|---|---|---|
| EGAS00001002628 | Other |
Study Description
2017 AML prospective study contains 10 paired WES samples which were collected from SNUH.The study was designed to examine the molecular abnormalities from leukemic patients at initial diagnosis in comparison with corresponding germ line control (saliva samples). The results of WXS were analyzed by Mutect for ranking cancer variants and creating mutational matrix.
Study Datasets 1 dataset.
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 |
|---|---|---|---|
| EGAD00001003598 |
This data is belong to 2017 AML prospective data which is aligned to human reference(human_g1k_v37.fasta).
There are 10 paired tumor/normal samples from SNUH.
All samples has passed QC and recalibration steps while aligning to reference.
|
HiSeq X Ten | 20 |
Who archives the data?
