@article {308681,
	title = {Multiple haplotype-resolved genomes reveal population patterns of gene and protein diplotypes.},
	journal = {Nat Commun},
	volume = {5},
	year = {2014},
	note = {http://www.nature.com/ncomms/2014/141126/ncomms6569/full/ncomms6569.html},
	month = {2014},
	pages = {5569},
	abstract = {<p>To fully understand human biology and link genotype to phenotype, the phase of DNA variants must be known. Here we present a comprehensive analysis of haplotype-resolved genomes to assess the nature and variation of haplotypes and their pairs, diplotypes, in European population samples. We use a set of 14 haplotype-resolved genomes generated by fosmid clone-based sequencing, complemented and expanded by up to 372 statistically resolved genomes from the 1000 Genomes Project. We find immense diversity of both haploid and diploid gene forms, up to 4.1 and 3.9 million corresponding to 249 and 235 per gene on average. Less than 15\% of autosomal genes have a predominant form. We describe a {\textquoteright}common diplotypic proteome{\textquoteright}, a set of 4,269 genes encoding two different proteins in over 30\% of genomes. We show moreover an abundance of cis configurations of mutations in the 386 genomes with an average cis/trans ratio of 60:40, and distinguishable classes of cis- versus trans-abundant genes. This work identifies key features characterizing the diplotypic nature of human genomes and provides a conceptual and analytical framework, rich resources and novel hypotheses on the functional importance of diploidy.</p>},
	keywords = {Cohort Studies, Diploidy, European Continental Ancestry Group, Genetic Variation, Genetics, Population, Genome, Human, Germany, Haplotypes, Humans, Mutation, Polymorphism, Single Nucleotide, Proteins},
	issn = {2041-1723},
	doi = {10.1038/ncomms6569},
	url = {http://www.ncbi.nlm.nih.gov/pubmed/25424553},
	author = {Hoehe, Margret R and Church, George M and Lehrach, Hans and Kroslak, Thomas and Palczewski, Stefanie and Nowick, Katja and Schulz, Sabrina and Suk, Eun-Kyung and Huebsch, Thomas}
}
