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Category:All HeadlinesWorld & GeopoliticsMarkets & EconomyTech & AIPoliticsSearch results for: "100,000 Genomes Pilot on" (30 stories)

Top Headline Story

Reanalysis of genomic data doubles the diagnostic yield for Welsh patients recruited to the UK 100,000 Genomes Project
Lead StoryNaturegeneral
Sep 28

Reanalysis of genomic data doubles the diagnostic yield for Welsh patients recruited to the UK 100,000 Genomes Project

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5yVEtzVnBpb3Z2ZDMtUkxuT21hSWhQWG5SQWw0aFR3aWZ2aTI0LUgtMzR1OWZ0X0tIdDRiV3ZFX1NkZFZWN1hZNXNpdG00eEZwendBQjVibEg4RGlEczRF?oc=5" target="_blank">Reanalysis of genomic data doubles the diagnostic yield for Welsh patients recruited to the UK 100,000 Genomes Project</a>  <font color="#6f6f6f">Nature</font>

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Search Results for "100,000 Genomes Pilot on"

Updated every 3 minutes via FreeNewsApi, GNews, Currents API & Google News

29 stories displayed
100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care — Preliminary Report
The New England Journal of Medicinescience

100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care — Preliminary Report

<a href="https://news.google.com/rss/articles/CBMiYEFVX3lxTE1RUUs4OGJITTl3VTgxR3dxQzlDY2FfbDVZOVVHYTFwai0xd1NPNS1hT2I5NE1DaWNScDdEVEk1M1RJRXI0cW04TnlBU0UybFI0Qm14MGVtTDVWTHk0cUVQMQ?oc=5" target="_blank">100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care — Preliminary Report</a>  <font color="#6f6f6f">The New England Journal of Medicine</font>

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Germany's Precision Medicine Pilot Project Gains Steam After Putting Data Infrastructure in Place
Genome Webtech

Germany's Precision Medicine Pilot Project Gains Steam After Putting Data Infrastructure in Place

<a href="https://news.google.com/rss/articles/CBMivgFBVV95cUxQTnU2YjVTZkl4RlFBQnp4RFZGejZTaFozUk9xU1Q2T2EzcVpJczRLWkFoZlU3MkR3TUhIMzFlWHZiMWV3azllSGNoOHFwbUhpeDJGOHo3d0Z3eXZUelhRSnNuOG4ycV9DUThyOXJXMUwycjBDc21xNjdtRFlkUE9kd0xRclRxZ2tQUnlNWW91X0NyUk5jRlJtV3poTlNOUFpaa1RNTkRBOGZ0eTk3d1lZcHR5MDN4Qkk3eHppb2ZR?oc=5" target="_blank">Germany's Precision Medicine Pilot Project Gains Steam After Putting Data Infrastructure in Place</a>  <font color="#6f6f6f">Genome Web</font>

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Sunshine Genetics Act Expands Newborn Screening to Hundreds of Treatable Genetic Diseases
University of Miamiworld

Sunshine Genetics Act Expands Newborn Screening to Hundreds of Treatable Genetic Diseases

<a href="https://news.google.com/rss/articles/CBMiuAFBVV95cUxOOTBEQnJvNGVsUkZxcUdoa29vbERTOVdWalFFOHUzc3dqejh0WnJDRF9wVmcxQjg5SXo4cVkySU44RWEwZ2c0cFB1LWFJMTBBamtkTVNuWXBRdW1mQ1JkenVOclQ0TkNTLVZvaTkxeTdMSU45LTRDRkFDbkxZbFRUeVM5amNNa2YyZUNaMlN5a3FCMHpMR05CNHdqcHBoQ2JsMmw4RkRjb0dpbGNDN21WdDJpUTJGbmtO?oc=5" target="_blank">Sunshine Genetics Act Expands Newborn Screening to Hundreds of Treatable Genetic Diseases</a>  <font color="#6f6f6f">University of Miami</font>

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Rare disease diagnosis by 100,000 genomes pilot
News-Medicalgeneral

Rare disease diagnosis by 100,000 genomes pilot

<a href="https://news.google.com/rss/articles/CBMimgFBVV95cUxNN25kNjdCaXdTX1pWMVI0SVAzZXNHb25MMUFCdkJ3SzJqVW1NTEVsRmtCSkVTSTR4Vm5icDJWaThpdVpKcWJXWGpkMTQ3WkpyT1dhX1pSRGtoM3VoQnBfbE1PUVU4UWsxUF9ZUlVBMWRIZWNOczZmN1ExeGVZemxqcXNLbzZJVjdUZ1hpX0pCYkJfR05VNU1raFRR?oc=5" target="_blank">Rare disease diagnosis by 100,000 genomes pilot</a>  <font color="#6f6f6f">News-Medical</font>

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Population-scale genomic medicine with the Hong Kong Genome Project
Naturegeneral

Population-scale genomic medicine with the Hong Kong Genome Project

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE50azR1QVNJelNYNTV2R0JPcFFqTGhlZkptQ1lJN25KZ3hhSmJrWkJLLXBHS2xweFpyYXhDdXVOV2ItTmVmY1lyN0VDZFB6NGtSRm9qRUljMXMxQTVHWGkw?oc=5" target="_blank">Population-scale genomic medicine with the Hong Kong Genome Project</a>  <font color="#6f6f6f">Nature</font>

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SVRare: discovering disease-causing structural variants in the 100K Genomes Project
medRxivgeneral

SVRare: discovering disease-causing structural variants in the 100K Genomes Project

<a href="https://news.google.com/rss/articles/CBMickFVX3lxTE9POWEwanR6bEhoR2dET2tzMVR1U0luX0RmWHZFZWE4Uno4UG02WnZ1Nm1lZHQxVlVEbjhzVm9KVm0xc25fTUhlbXIxV1lGeFlNTnlXeUh2MGNDR2plQ0d0R3BzRXhrLWRqSy1mdUxyakZidw?oc=5" target="_blank">SVRare: discovering disease-causing structural variants in the 100K Genomes Project</a>  <font color="#6f6f6f">medRxiv</font>

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Genomics England Selects Omicia and University of Utah Technology for 100,000 Genomes Project
University of Utah Healthtech

Genomics England Selects Omicia and University of Utah Technology for 100,000 Genomes Project

<a href="https://news.google.com/rss/articles/CBMiwAFBVV95cUxOZVlhRkIzLUtpNWJwdElCMmR0MDlqRXAyZTZHMmtYTXk4bmVDY3ZIV1NkQ3ZmdGRNZFNXUnR3bjd2a3FERGlhbGwySEtuOFdsekUwbnlUaVA3TzdOSEpBUVdXLS1TUmNrdEYyQVF2SVdtYU81UGRGemZIX3BkYWVhX1JFZkI4b3EwazNMVVV5STYwcVlQTkltT1NqRm5WXzJkbXVrcm13WEZ5MzdZOVNEU0RaRFdLQTNQNFdjUEF5dWk?oc=5" target="_blank">Genomics England Selects Omicia and University of Utah Technology for 100,000 Genomes Project</a>  <font color="#6f6f6f">University of Utah Health</font>

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Rare disease gene association discovery in the 100,000 Genomes Project
Naturegeneral

Rare disease gene association discovery in the 100,000 Genomes Project

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE82bXBRcUlMb2EwUnRVTEdDeV9QN0JSakZuSG1heGwySlk0SzVBamNBMlB3QU9UODNIa2daaGY0RXpWcF9LRG9ZaVgzLXVlYVF0SkQ2czBIYS1lRGhUbjFB?oc=5" target="_blank">Rare disease gene association discovery in the 100,000 Genomes Project</a>  <font color="#6f6f6f">Nature</font>

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100,000 whole-genome sequences’ diagnostic bonus
Naturegeneral

100,000 whole-genome sequences’ diagnostic bonus

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5PeWtfNVVPRWNZVWtQQ0pOQXY4LUpqMEJ0Nl8teTIxMEpHdTREVTBfYkhNdkxZU1ZXanhwUXJHV0k1dzZsOVAzVHpoMUhIaDRVSE5uVC1VVXFSWHNWM1Iw?oc=5" target="_blank">100,000 whole-genome sequences’ diagnostic bonus</a>  <font color="#6f6f6f">Nature</font>

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Insights for precision oncology from the integration of genomic and clinical data of 13,880 tumors from the 100,000 Genomes Cancer Programme
Naturegeneral

Insights for precision oncology from the integration of genomic and clinical data of 13,880 tumors from the 100,000 Genomes Cancer Programme

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE56QVlwY2ExdkZLMnB4UEZWR1pwNU16Si01T1hXZGtGZU1XVDRVVkJPQlByODNQbkVLeG91b3k0bklJYU1sdl9aemlhWkpmZkQ4anhaQ3JkSUp5aXg3aVNZ?oc=5" target="_blank">Insights for precision oncology from the integration of genomic and clinical data of 13,880 tumors from the 100,000 Genomes Cancer Programme</a>  <font color="#6f6f6f">Nature</font>

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The potential clinical utility of Whole Genome Sequencing for patients with cancer: evaluation of a regional implementation of the 100,000 Genomes Project | British Journal of Cancer
Naturegeneral

The potential clinical utility of Whole Genome Sequencing for patients with cancer: evaluation of a regional implementation of the 100,000 Genomes Project | British Journal of Cancer

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFBYMFFMUnJlTERfSHpxVW9ObUxpS2otYTJucWliXzFWTnhuTm15VXUzaHBUemxVMm9EX2dCLXpwdjdNTjJKU1hoU0FyRnJnYnZGY21NblNpaU15blFvU2dj?oc=5" target="_blank">The potential clinical utility of Whole Genome Sequencing for patients with cancer: evaluation of a regional implementation of the 100,000 Genomes Project | British Journal of Cancer</a>  <font color="#6f6f6f">Nature</font>

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The NHS England 100,000 Genomes Project: feasibility and utility of centralised genome sequencing for children with cancer | British Journal of Cancer
Naturegeneral

The NHS England 100,000 Genomes Project: feasibility and utility of centralised genome sequencing for children with cancer | British Journal of Cancer

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE9TOGdFcUpnLWZ1RWxaMnZpOWNpY2tZMlpxbEQ2VHN3MVRKcnQwenRXMFJtYjJzZmtwQ3Z6Rlh1Yk92d3VBUEI2MUlXMWtVb292M3h6Z1VyYmYwaEQ2Vzkw?oc=5" target="_blank">The NHS England 100,000 Genomes Project: feasibility and utility of centralised genome sequencing for children with cancer | British Journal of Cancer</a>  <font color="#6f6f6f">Nature</font>

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Genome sequencing with gene panel-based analysis for rare inherited conditions in a publicly funded healthcare system: implications for future testing | European Journal of Human Genetics
Naturescience

Genome sequencing with gene panel-based analysis for rare inherited conditions in a publicly funded healthcare system: implications for future testing | European Journal of Human Genetics

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5jX1JsU1VZU0Y4WUg5ZTZSbFRNZEljM1JMX3hTUXl0R1h0Tll3TENFblc2aDJzMUdEUUExZWlSRUUzVE5iUkFPZE5sdDJaWnJrS2hwQ2hnQ2RCOXlHOTZF?oc=5" target="_blank">Genome sequencing with gene panel-based analysis for rare inherited conditions in a publicly funded healthcare system: implications for future testing | European Journal of Human Genetics</a>  <font color="#6f6f6f">Nature</font>

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100,000 genomes — in Africa, for Africa
Naturegeneral

100,000 genomes — in Africa, for Africa

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE42S0RCUVY1WkFGS2xzVVowMEZsT1pSR2ZNRnhpcnR6TzcwdVEwRVl4eWk3Yml2aWYybE5aRDJHcWxyM3NwTi1udE9kRHAxS1NyRWZnM0hibkdzamNHRExF?oc=5" target="_blank">100,000 genomes — in Africa, for Africa</a>  <font color="#6f6f6f">Nature</font>

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A roadmap for genome projects to foster psychosocial and economic evidence to further policy and practice
Naturegeneral

A roadmap for genome projects to foster psychosocial and economic evidence to further policy and practice

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE10MnBGSVBsUUhGaC0ydUZ5Ml9vXzNKRlJuRnJVRlVIM09SR1c2dnRiMVNyMll6S1JpRzA0RzdJYWw0NDlpRkt6UEZBWnBpa2ltSFZCRWUzUk10amRxQUdn?oc=5" target="_blank">A roadmap for genome projects to foster psychosocial and economic evidence to further policy and practice</a>  <font color="#6f6f6f">Nature</font>

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Evaluating the performance of a clinical genome sequencing program for diagnosis of rare genetic disease, seen through the lens of craniosynostosis
Naturegeneral

Evaluating the performance of a clinical genome sequencing program for diagnosis of rare genetic disease, seen through the lens of craniosynostosis

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5jdU16LWtSOE54SWgtME84eThwVGh4c0lieDl4Mnc0Q1pobm9FOTVwOGdnTUNfWG1ON3djYXhPMVFQdWJUd0FJOElKTnFNc2RMUXdxcnIxQTFDdmQ2clJV?oc=5" target="_blank">Evaluating the performance of a clinical genome sequencing program for diagnosis of rare genetic disease, seen through the lens of craniosynostosis</a>  <font color="#6f6f6f">Nature</font>

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Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project
Natureworld

Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE4xRDlvYUZCQlZBWl9ES1dabDdrdktkYzJOOV9DejY2d1N3SWFQLWsxWFZmNlVOMl9mMkFRRFZ6N1BTTWREeHRZd19HRWZzeEdMbUw3RjZrOE5pZ3dLdDQ4?oc=5" target="_blank">Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project</a>  <font color="#6f6f6f">Nature</font>

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The GenomeAsia 100K Project enables genetic discoveries across Asia
Naturegeneral

The GenomeAsia 100K Project enables genetic discoveries across Asia

<a href="https://news.google.com/rss/articles/CBMiXkFVX3lxTFBzMHh5ZUdQQThQSTdNT09XclhWNmhJaWtEY1RPcFF1Z05GdmR1Z0hKekNwazRaeEc0bUZLN3Fsa09lcG4xdkhzcmlSa1hfQ3ZMdThYY3RXT0tQZUppeUE?oc=5" target="_blank">The GenomeAsia 100K Project enables genetic discoveries across Asia</a>  <font color="#6f6f6f">Nature</font>

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UK launches whole-genome sequencing pilot for babies
Natureworld

UK launches whole-genome sequencing pilot for babies

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5pTUhZM1BkRmI3Z3hTZXFZZV9FcEpiWjJIcXVuQk13eW9LWTlSSnRDYU81LThxaTBqVUZfMVZiX2l3dE91cnRWTWlnQjdkSV9UbEN1cFdraVdFS0hjYmRz?oc=5" target="_blank">UK launches whole-genome sequencing pilot for babies</a>  <font color="#6f6f6f">Nature</font>

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Clinical Sequencing’s Ups and Downs Around the World
Inside Precision Medicineworld

Clinical Sequencing’s Ups and Downs Around the World

<a href="https://news.google.com/rss/articles/CBMirwFBVV95cUxQd1dJdXhkMEFET3ZoRkZicGRYNHhtaUs2NjllZ3AxY3g2NlRhMzR4eXFVMmUzSmJ0V29xS0dGSi1yUDJrZjZRbWJOaHVLM0NkZmgtRWFuQl9Fd1F3aVB4S0JNa3Q2Mk10ZkFoWjJlWEFJcFlBbDB5MElYcWQxSDVlY0lKcUwxVzNEN2F0X1dqNkRka2c5Y3pGV2lmR2FROU1wcjhGYm1yY3NMeGpueFM4?oc=5" target="_blank">Clinical Sequencing’s Ups and Downs Around the World</a>  <font color="#6f6f6f">Inside Precision Medicine</font>

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Genomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland
The New England Journal of Medicineworld

Genomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland

<a href="https://news.google.com/rss/articles/CBMiYEFVX3lxTFBZUEM0cFhZcjdxcXFSYlZpRTN4RWhCendKdHBfQmRaRTdKbDBpNE0zcHFXcVZFSXpjZUl1eDdSMDlmWUcxX0JfNlFuOVMwRkN2TGNETkpMenBzVU5uWjJfNA?oc=5" target="_blank">Genomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland</a>  <font color="#6f6f6f">The New England Journal of Medicine</font>

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Genetic association analysis of 77,539 genomes reveals rare disease etiologies
Naturegeneral

Genetic association analysis of 77,539 genomes reveals rare disease etiologies

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE96Qm0xajhkdUJsNUd5RGtObXFCWURXVDV0RjZfMUo0U0hXY2c2T1BGc1dkZ3o0bEZFQ0xLejVpNktIRzZveDJVV3pUV2Q2eWpsZFJtN1g4aDd6TFFKMHlr?oc=5" target="_blank">Genetic association analysis of 77,539 genomes reveals rare disease etiologies</a>  <font color="#6f6f6f">Nature</font>

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The Value of Bio Big Data in Rare Disease Diagnosis and Treatment
3billiongeneral

The Value of Bio Big Data in Rare Disease Diagnosis and Treatment

<a href="https://news.google.com/rss/articles/CBMikwFBVV95cUxQZUNxU2VzaE9GWjdsVmYyUVA3VU4tNWx0ZlpJQm5jZmlfT18zT0lPQnJFYzVZTzJkVFdpNlVtLS1kb1l2YU41Ny0yb3FRSjF4ejRWbXMzVTVLOFpRamZFbVdqd3dLY0VTRkdGQlU3bXZ5OGZHWlhJOFNfNnVoS1YzT1U0cW9TTjlsNEg2bFU1X1gyX2s?oc=5" target="_blank">The Value of Bio Big Data in Rare Disease Diagnosis and Treatment</a>  <font color="#6f6f6f">3billion</font>

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Computational biology in rare disease research
News-Medicalgeneral

Computational biology in rare disease research

<a href="https://news.google.com/rss/articles/CBMikAFBVV95cUxPWWRGZ3BtV3BlR3VTcC00TnJ5Q2NWYnlXOTZnMFdQeU91aGRTWDFNWTBzOUZzX3l5UnYxcjVOV2VqRUw1azFxUGtuY2VwVFJ1V0F1bEYwZy1hZzVkZVBUZlItYzNjTlFIbzY0dUZjbDB3QjhGUnlndjFWWjVzOXc5QlFDckVDdUVmRjRnRjFjZUU?oc=5" target="_blank">Computational biology in rare disease research</a>  <font color="#6f6f6f">News-Medical</font>

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Genomics England Taps Edico Genome for Rare Disease Pilot
Inside Precision Medicinegeneral

Genomics England Taps Edico Genome for Rare Disease Pilot

<a href="https://news.google.com/rss/articles/CBMitwFBVV95cUxOUFRiOTU2T21Ia19zWU13UmFDRElZN01ITWZHeFhmSDczTTZKRTlYV3dSNjFJYkZ3REs5WUdiUHpoVVFPdGhjUkl2RUlpM1pMcDJTNU11SFpZUXJUYm5WVExPLVBfSVNYS1oyRkRfbmp3MWhuQ0FCcWtXY3RuSDNtb0RwTnRvNVZKSVVZVW1VbHdOMkYxR3RsMHlGNHFxb0FlQmFJUzZaWXBKSWFnZENwWTVma09pV0U?oc=5" target="_blank">Genomics England Taps Edico Genome for Rare Disease Pilot</a>  <font color="#6f6f6f">Inside Precision Medicine</font>

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Analysis of R-loop forming regions identifies RNU2-2P and RNU5B-1 as neurodevelopmental disorder genes
medRxivgeneral

Analysis of R-loop forming regions identifies RNU2-2P and RNU5B-1 as neurodevelopmental disorder genes

<a href="https://news.google.com/rss/articles/CBMie0FVX3lxTE5KR0dxclExUmFXNHNoVEJnU2REcjY1VkxBV0t4ZWlKbllfel9SRGI0djIxXy01Yk1MZnVPY0E1cllha2FmaExQNmo5RjNTbmpEWGRzZ3BRcXU2UFBpek9kd3RhZjNPbnNGQmp4YXh0eWM5Zndna3prSXdOQQ?oc=5" target="_blank">Analysis of R-loop forming regions identifies RNU2-2P and RNU5B-1 as neurodevelopmental disorder genes</a>  <font color="#6f6f6f">medRxiv</font>

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The co-occurrence of genetic variants in the TYR and OCA2 genes confers susceptibility to albinism
Naturegeneral

The co-occurrence of genetic variants in the TYR and OCA2 genes confers susceptibility to albinism

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5tOG9HeFJ1T29oNjZwSmR2WWRvd2JpODI5alc5WngzY290SHVtZTh3T2FxVEJZS2dHU2RBUDZEXzZsYXFzZHZOTC1JMDN0TGRIelJoRURkN29fUFRub3k0?oc=5" target="_blank">The co-occurrence of genetic variants in the TYR and OCA2 genes confers susceptibility to albinism</a>  <font color="#6f6f6f">Nature</font>

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Whole genome sequencing improves diagnosis of rare diseases and…
Genomics Englandgeneral

Whole genome sequencing improves diagnosis of rare diseases and…

<a href="https://news.google.com/rss/articles/CBMijgFBVV95cUxNd0FsbWFLTVpYcm9fMEhQb19YeGp3Rl9XRnRtdmEtODRQOTdKUUlrcVlhZFBRenBYU3RRaUZDbk5ub2N6U0FXR0F2MkdVMUxSdHNrUE1tVE9zRzFDODA3ZVU3cXhOTnd1LVBhWm9jWEZ1R1d0RGg5VnVESTdVS21ON3BkZTR6cGROOUVUNnRR?oc=5" target="_blank">Whole genome sequencing improves diagnosis of rare diseases and…</a>  <font color="#6f6f6f">Genomics England</font>

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Industry collaboration already benefiting participants of 100,000…
Genomics Englandgeneral

Industry collaboration already benefiting participants of 100,000…

<a href="https://news.google.com/rss/articles/CBMiiwFBVV95cUxQYkFIaVBjX2U2THRXdllqYUstR3lBMXZOcDBLNVV1aXZDelN3aGpfVFhDaVNDdGZMdWRvWXdPT1ZoLXY1SldHVlByT2hKLTVZZVZFaW1mYWJ6alZwR0ZVbWQzYWRuWi0yeWxVcm5rV0xWa3dGLXFBMFljSnNXaVBuM016WUNwT2lYdjN3?oc=5" target="_blank">Industry collaboration already benefiting participants of 100,000…</a>  <font color="#6f6f6f">Genomics England</font>

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"100,000 Genomes Pilot on" — Live Google News Trends & Headlines