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.

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Dataset ID Description Technology Samples
Datasets Galaxy 929/938 describe the amplified single chromosome sequencing data.

Who archives the data?

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