Project name: Homo sapiens

Description: We performed whole-genome sequencing of sixteen individuals drawn from a 13-generation pedigree. Fifteen of these individuals comprise five parent-offspring trios. We generated 10-15X effective sequence coverage of the genome for each of these sixteen individuals using Illumina HiSeq paired-end reads. Using these sequence data, we have performed genetic variant detection for single nucleotide variants, indels, and copy number variants.

Data type: Phenotype or Genotype

Sample scope: Multiisolate

Relevance: Medical