2015
DOI: 10.1186/s12864-015-1973-7
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Crowdsourced direct-to-consumer genomic analysis of a family quartet

Abstract: BackgroundWe describe the pioneering experience of a Spanish family pursuing the goal of understanding their own personal genetic data to the fullest possible extent using Direct to Consumer (DTC) tests. With full informed consent from the Corpas family, all genotype, exome and metagenome data from members of this family, are publicly available under a public domain Creative Commons 0 (CC0) license waiver. All scientists or companies analysing these data (“the Corpasome”) were invited to return results to the … Show more

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Cited by 20 publications
(29 citation statements)
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“…Such considerations absolutely do not negate the enormous potential for applying genomics in a public health context-but they do imply that a signifi cant measure of caution should be applied as we pursue this exciting prospect. It is clear that at present we do not know how to interpret the results of genome-scale sequencing in the healthy population; our inability to reliably assign pathogenicity to variants, the tendency toward overinterpretation, misinterpretation, and our simple lack of knowledge about the natural history of most genetic disorders argue convincingly that it is premature to implement genome-scale sequencing in healthy individuals outside the realm of research [3,[37][38][39][40]. However, we do have a reasonably solid grasp of what the implications are for individuals who carry a pathogenic variation in a few of the approximately 22,000 human genes.…”
Section: Resultsmentioning
confidence: 99%
“…Such considerations absolutely do not negate the enormous potential for applying genomics in a public health context-but they do imply that a signifi cant measure of caution should be applied as we pursue this exciting prospect. It is clear that at present we do not know how to interpret the results of genome-scale sequencing in the healthy population; our inability to reliably assign pathogenicity to variants, the tendency toward overinterpretation, misinterpretation, and our simple lack of knowledge about the natural history of most genetic disorders argue convincingly that it is premature to implement genome-scale sequencing in healthy individuals outside the realm of research [3,[37][38][39][40]. However, we do have a reasonably solid grasp of what the implications are for individuals who carry a pathogenic variation in a few of the approximately 22,000 human genes.…”
Section: Resultsmentioning
confidence: 99%
“…Motif discovery analyses were performed on Orion Integrated Biosciences servers using MF generation (MF-gen) and CHAST algorithms to identify protein fragments associated with precise taxonomies via an exhaustive search of GenBank protein databases as described in Corpas et al (58) and Wilson et al (36). Briefly, all protein entries in GenBank were divided into 12-amino acid subsequences (motifs) that were position-independent and did not contain overlaps.…”
Section: Methodsmentioning
confidence: 99%
“…We performed this procedure for four "real-world" trios with publicly available exome data: the Ashkenazim trio HG002_NA24385 from the Genome in the Bottle project [13] ("AJT"), the YRI_NA19240 trio from the 1000 Genomes project [14] ("YRI"), the CHD trio [15] ("CHD"), and the Corpas family daughter trio [16] ("Corpas"). Since the child in the "real-world" trios was either a living individual (AJT, YRI, Corpas) or stillborn (CHD), there was no maternal cell contamination in the "real-world" reads.…”
Section: Contaminated Trio Generationmentioning
confidence: 99%