Haplotype phasing of an individual human genome
Source: NCBI BioProject (ID PRJEB2404)

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Project name: Phasing MP1
Description: We have established a novel fosmid-based approach to haplotype resolve whole genomes directly by next generation sequencing (NGS). Variant positions (SNPs, indels and CNVs) within the genome are detected, and identical alleles at heterozygous, haplotype-informative positions allow the haploid fosmids to be assigned to one of two physical haplotype sequences. This prepares the foundation to tile overlapping fosmids into long contiguous molecular haplotype sequences.
Data type: Other
Sample scope: Monoisolate
Organization: Max Planck Institute for Molecular Genetics
Release date: 2011-01-20
Statistics: 1 sample; 1 experiment; 1 run