supplementaryTable7.pdf (489.69 kB)
Supplementary Table 7. WGS data
dataset
posted on 2017-12-22, 13:27 authored by Anuradha Jagadeesan, Ellen D. Gunnarsdóttir, S. Sunna Ebenesersdóttir, Valdis B. Guðmundsdóttir, Elisabet Linda Thordardottir, Margrét S. Einarsdóttir, Hákon Jónsson, Jean-Michel Dugoujon, Cesar Fortes-Lima, Florence Migot-Nabias, Achille Massougbodji, Gil Bellis, Luisa Pereira, Gísli Másson, Augustine Kong, Kári Stefánsson, Agnar HelgasonAmong the 182 descendants, 20 of them had been whole genome sequenced, aligned and mapped to NCBI Build 38 of the human genome. The mean and standard deviation (SD) for the number of reads per position (sequence depth) are given for each of them, along with the number of autosomal positions covered by mapped reads.
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Human GeneticsHuman ancestrygenetic variation datasetGeneaologyAfrican microarray SNP datasetsingle nucleotide polymorphismgenetic variantsIcelandic populationAfrican ancestrydense genetic dataadmixed populationsancestry fragmentSNPwhole genome sequenceWGSgenome reconstructionIcelandic ancestrychromosome fragmentsphased source population genotype data
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