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genome sequencing genome analysis genomic data rare diseases genome interpretation personalized medicine genomics nextcode health decode genetics wuxi nextcode genomics england cancer genome database nextcode exchange genome data storage genetic variants genomic analysis sidra medical and research center genomically ordered relational database (gor) nextcode big data 000 genomes project genomic data sharing genomics-driven medicine genetic variation 23andme clinical sequencing whole genome sequencing wuxi genomic medicine data storage genome storage genomics-based medicine human genome population-scale sequencing boston children's hospital cancer tumor analysis national cancer institute next-generation sequencing gene sequencing genomic data analysis baylor college of medicine charlotte & gwyneth gray foundation plos blog clinical genomics national patient-centered clinical research networ biocentury global medicine large-scale sequencing spark genoimc data acord anzac research institute bio-it world xconomy stanford school of medicine cloud-based analysis data sharing population genomics ashg 2016 parent project muscular dystrophy hannes smarason patient-centric communities genetic datasets rareconnect simons foundation autism research initiative patientslikeme raw sequence data whole exome sequencing low-cost genome sequencing genomic sequencing and analysis genetics of disease genomic research centers genetic mutations and disease mygene2 whole-genome sequencing gene variants 100 d wuxi nextcode genetic alliance nature biotechnology autism integrated approach to genomics-based care for rar global genes claritas genomics and nextcode have established a pediatric genetic disorders the partnership aims to accelerate and augment the genomics-based care diagnostic odyssey mayo clinic fda claritas genomics 10 fudan children’s hospital qatar genome project national institutes of health precision medicine clinical oncology asco her2 testing brca testing efgr testing tapur alk testing genetic testing charcot-marie-tooth syndrome tumor profiling genetic diseases genome databases illumina data silos dtc genetic testing bloomberg regeneron human longevity 100000 genomes project rare genetic diseases genetic variant 100k genomes project saitama medical university university college dublin carrier status queensland institute of medical research haplotype reference consortium (hrc) whole-genome databases genomic-based medicine american society of human genetics (ashg) autism spectrum disorder simons simplex collection nci-match