Study
Acquiring and sequencing of all 24 single human chromosomes
| Study ID | Alternative Stable ID | Type |
|---|---|---|
| EGAS00001003300 | Other |
Study Description
Haplotype phased whole genome sequencing of individuals is a technical challenge when family members are unavailable for determining chromosome of origin and variant linkage. Completely phasing genome sequences with single chromosomes has been shown to be feasible however amplifying all the single chromosomes for subsequent whole genome sequencing has been proposed but not performed to date. We acquired single chromosome of one of each of the autosomes and sex chromosomes to assess the feasibility of this sequencing library template preparation process.
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 |
|---|---|---|---|
| EGAD00001004457 |
Datasets Galaxy 929/938 describe the amplified single chromosome sequencing data.
|
2 |
Who archives the data?
