| identifier | PRJEB2404 | ||||||||||||
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| type | bioproject | ||||||||||||
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| title | Haplotype phasing of an individual human genome | ||||||||||||
| 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 | ||||||||||||
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| distribution | JSONJSON-LD | ||||||||||||
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| status | public | ||||||||||||
| visibility | unrestricted-access | ||||||||||||
| dateCreated | 2011-01-20T00:00:00Z | ||||||||||||
| dateModified | 2011-01-20T00:00:00Z | ||||||||||||
| datePublished | 2011-01-20T00:00:00Z |