bioRxivBioinformaticsPreprint
Personal genomics: new concepts for future community data banks
Abstract
INTRODUCTION INTRODUCTION SPLIT GENOMIC DATA TRANSACTIONS BETWEEN COMMUNITY... RESULTS AND DISCUSSION REFERENCES The advent of fast, low-cost sequencing techniques is boosting the number of sequenced human genomes thus driving the irresistible push towards personalized genomics and personalized medicine.1 The examination of the genomes of large cohorts of patients will permit to identify the origins of many diseases and to propose adapted, fine-tuned medical treatments. The genomic boom is also expected to generate an economic activity worth billions of dollars and a fierce race has already started between Internet giants like Google and Amazon. Big data companies have already gathered tens of thousands of individual human genomes hosted in the cloud (that is on a server accessible via the Internet) and th ...
- organism: human
- assay: whole-genome sequencing
- research focus: GWAS / association mapping
- research focus: variant calling
- Citations
- 1
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Genomics in healthcare: GA4GH looks to 2022
Ewan Birney, Jessica J. Vamathevan, Peter Goodhand·bioRxiv·Oct 15, 2017
- PGP-UK: a research and citizen science hybrid project in support of personalized medicine
Stephan Beck, Alison Berner, … John N. Wood·BMC Medical GenomicsPeer-reviewed·Nov 27, 2018
- 10 Simple Rules for Sharing Human Genomic Data
Manuel Corpas, Charlotte Whicher, … Varsha Khodiyar·bioRxiv·Jan 12, 2017
- Advancing clinical cohort selection with genomics analysis on a distributed platform
Jaclyn Smith, Melvin Lathara, … Christopher T. Denny·PLoS ONEPeer-reviewed·Apr 23, 2020
- A Complete Public Domain Family Genomics Dataset
Manuel Corpas, Mike Cariaso, … Huanming Yang·bioRxiv·Nov 12, 2013
- DNA Compass: a secure, client-side site for navigating personal genetic information
Charles Curnin, Assaf Gordon, Yaniv Erlich·bioRxiv·Sep 27, 2016