262 结果
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Illuminating Rare Disease
Bringing to light the challenges and hopes for the rare disease community
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Shriners医院启动大型测序项目
基因组学杰出人物Marc Lalande博士和Kamran Shazand博士利用Trusight软件套装建立了基因组学研究所，这个美国的标志性医疗系统将推动从墨西哥城到蒙特利尔等更多地区的研究和个性化医疗。
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燃石医学与因美纳深化合作，推进肿瘤基因检测行业发展和规范前行
广州燃石医学检验所有限公司（以下简称“燃石医学”）和全球基因测序和芯片技术的领先企业因美纳（Illumina），共同宣布基于NextSeq™ 550Dx测序系统的合作，携手推进国内肿瘤高通量测序（Next Generation Sequencing，NGS）行业的发展和规范前行。
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The Weizmann Institute Uses NovaSeq to Drive Single Cell Research
By analyzing one cell at a time, Professor Amit is improving our understanding of biological systems in health and disease
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Illumina Registers MiSeqDx Instrument in Japan
Two Next-Generation Sequencers Now Available for In Vitro Diagnostics
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Texas A&M Deploys DRAGEN
First American Academic Institution Install for Agricultural Applications
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Illumina Hosts Calif. Assembly Select Committee on Biotech & Rare Disease Caucus
Project Baby Bear briefing highlights progress and impact
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BaseSpace Sequence Hub Now Locally Available in Australia
Secure, scalable data management and analysis – now hosted locally in Australia
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Illumina @ A Glance
Infographic provides snapshot of the company, its markets, its portfolio and more
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Careers of the Future - An Illumina Spotlight Series
Get to Know Jakob Nielsen, Territory Account Manager
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Project Baby Bear – California Pilots Public Health Coverage for WGS
Q&A with Kathy Lynch, VP of Global Government Affairs & Public Policy at Illumina
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How Diversity in Science Can Benefit Communities
Illumina Researcher Marlem Rivera Shares Her Story
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The Power of iHope
The iHope Network Continues to Uncover the Mysteries of Rare and Undiagnosed Diseases
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University of Melbourne and Illumina Drive Genomics Innovation in Australia
This Partnership is Based on International Reach, Clinical Utility, Data Generation and Talent Development
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Careers of the Future – An Illumina Spotlight Series
Get to Know Alicia Scocchia, Genetic Counselor
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Careers of the Future - An Illumina Spotlight Series
Get to Know Daniel Brami, Bioinformatician
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Careers of the Future - An Illumina Spotlight Series
Get to know Greg Apker, Artificial Intelligence Engineer
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NovaSeq Spotlight: Investigating Causes of Male Infertility
Researchers at Newcastle University are Looking into Genetic Factors of Male Infertility
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The March of Dimes Birth Defects Foundation of China Selects Illumina as Its Partner
New Program will use Next-generation Sequencing in Genetic Detection of Birth Defects
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Careers of the Future - An Illumina Spotlight Series
Get to know Rita Pitts, Clinical Lab Scientist
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Illumina Registers NextSeq 550Dx Instrument in Japan
The First In Vitro Diagnostic Registered Instrument for Illumina Japan
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Influence of Panel Size on TMB Measurement
The importance of gene panel size in precisely measuring tumor mutational burden (TMB) in cancer composition
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Genomics Podcast: Eczema and the Human Skin Microbiome
Understanding the impact of the skin microbiome and human health
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NovaSeq Spotlight: Understanding Leukemia
Munich Leukemia Laboratory uses whole-genome research to drive future personalized treatment for patients
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GeneSeeq and Illumina to Develop Clinical Oncogene Kit
Accelerate The Launch Of Cancer NGS Testing in China
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Illumina Announces New NovaSeq Flow Cell
Extended kit configurations provide increased flexibility and utility for high throughput sequencing
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Watch President and CEO, Francis deSouza Speak at HLTH
An in-depth conversation about the future of genomics with CNBC's Meg Tirrell
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Fast Forward to the Future of Genomic Analysis
Speeding-up, standardizing and sharing NGS results with DRAGEN
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Education is Key to Non-invasive Prenatal Testing
Q&A with Illumina's Gautam Kollu and Carolyn Dumond
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Enabling Precision Oncology Through Companion Diagnostics
By: Garret Hampton, Executive Vice President of Clinical Genomics and Dr. Phil Febbo, Chief Medical Officer at Illumina
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个人基因组公司 WeGene 宣布将与 Illumina 建立战略合作，服务亚洲市场
WeGene Selects Illumina’s microarrays for a new laboratory in Asia.
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Registration of NextSeq™ 550Dx Sequencer in S. Korea
Illumina Grows Clinical Portfolio in South Korea
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Estonia Offers 100,000 Residents Free Genetic Testing
Effort aims to develop personalized medicine in national healthcare
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Illumina Partners with Chinese Assoc. of Medical Geneticist
First Consensus on Clinical Application of Sequencing in Children with Rare Diseases
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Celebrating Women in Genomics on International Women's Day
Illumina honors the contributions of women pushing the limits in science and engineering
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Illumina Supports ACOG Position Statement on Genetic Testing
Opposes payer-mandated access restrictions
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Study Assesses Newborns with Suspected Rare Diseases
Can Clinical Whole Genome Sequencing Change Care?
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Landmark 100,000 Genomes Project Reaches Halfway Milestone
Illumina and Genomics England partnership sequences 50,000 genomes
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NovaSeq S1 Flow Cell Delivers Speed and Flexibility
Powers Faster Runs and Smaller Sample Batching for High-Throughput Applications
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Sequencing Vital Fish Species Aims to Improve Livelihoods
Dr. Vanina Villanova wins 2018 Agriculture Greater Good Initiative Grant
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Advanced Materials Science – A New Genomics Frontier
Illumina Accelerator Graduate, Checkerspot, is Designing High-Value Materials
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Illumina and Harvard Pilgrim Partner on Value-Based Contract
Announce first ever next-generation sequencing agreement for non-invasive prenatal testing
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Adventures in Genomics: A New Look at Nature's Treasures
Illumina travels to China to learn how traditional medicine is using whole-genome sequencing
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Illumina Educates Elected Officials
How WGS may help children with rare and undiagnosed genetic diseases
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Illumina in France
New Solutions Center will train up to 1,000 scientists a year in latest genomics technologies
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Illumina and Pillar Biosciences, Inc. Announce Agreement
Pillar Biosciences to Collaborate with Illumina on Next-Generation Sequencing Based In Vitro Diagnostics Development
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BaseSpace Sequence Hub Helps Helix Conduct Consumer Genetics
Increased analysis automation features help streamline laboratory operations in high-volumes
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All in the Yeast
A good beer is all about the yeast, but can applying next generation sequencing lead to better beers?
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Adventures in Genomics: Untangling Alzheimer's Secrets
Learn about how genomics is being used in research of this devastating disease
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World Alzheimer’s Day 2017
Illumina demonstrates the company's support for the Alzheimer’s community
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Illumina Streamlines Nucleic Acid Quality Analysis
Illumina Partners with Advanced Analytical Technologies to Deliver Scalable Quality Assessment Solutions
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Study Takes Complete Look at Fetal Chromosomal Abnormalities
Paper Published in Science Translational Medicine
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BaseSpace Variant Interpreter Now Available
BaseSpace Variant Interpreter Launches for General Availability Following Milestone at Genomics England
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Selective Advantages in Cattle Breeding
Adventures in Genomics travels to Brazil to learn how genomics is revolutionizing agriculture in the area.
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Adventures in Genomics: Darwin on Our Doorstep
The littlest creatures still have a large impact on ecology. Learn how DNA is being used to help save the island fox.
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Video: MetaSUB - Molecular Portraits of World Cities
Using NGS to map Stockholm’s subway microbiome
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Illumina and Philips team up with Navican
Illumina and Philips team up with Navican to Accelerate the Delivery of Precision Medicine to Health Systems Worldwide
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VIDEO: Genomics to Enhance Global Food Security
Illumina donates HiSeq® 4000 Sequencer to Africa Orphan Crops Consortium and Opens Applications for 2018 Grant Program
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Illumina, IDT Partner on NGS Multiplexing & Exome Enrichment
Leaders in NGS and oligo manufacturing will optimize NGS library multiplexing and co-market exome enrichment methods
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Illumina Receives ISO 27001 Certification on its Information security management system
Illumina also announces that a European instance of BaseSpace Sequence Hub is now available
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Tracking Infectious Diseases with the MiniSeqTM System
University of Florida Professor Mattia Prosperi puts his MINI Cooper to work to improve public health
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Almac Diagnostics Leverages TruSight® Tumor 170
Recently launched panel aims to advance clinical cancer research
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Illumina Foundation at the Cambridge Science Festival
UK Families Learn About the Impact Genomics Promises for Future Healthcare
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Illumina Foundation Helps San Diegans Engage with Genomics
Sponsorship of Biocom Institute Festival of Science and Engineering inspires children and adults to think about DNA
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iHope Program Aims to Diagnose Rare Diseases in Children
Dana’s story illustrates power of next-generation sequencing to end diagnostic odysseys
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VIDEO: ALS Ice Bucket Challenge Two Years On
How ProjectMinE is making new discoveries using Illumina’s whole genome sequencing
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The Role of Genetic Counseling in Reproductive Healthcare
A Q&A with Illumina genetic counselor Patricia Winters
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TruSight RNA Fusion Comprehensive Panel for Fusion Detection
Provides in-depth assessment of 500+ genes associated with fusions
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TruSight® RNA Fusion: Cancer Panel for Gene Fusion Detection
Provides in-depth assessment of 500+ genes associated with fusions, delivered in a simple report
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Clinical Research Aims to Find New Drivers of Disease
Researchers at Children’s Mercy Kansas City Use Integrated Genomics Approach
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Illumina Honors Women in STEM
Ada Lovelace Day- a celebration of women in science and technology
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Chicago Shedd Aquarium Studies Microbes’ Effect on Sea Life
First-of-its-kind project is identifying microbial communities to improve health of aquatic animals
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San Diego Welcomes Festival of Genomics
Program highlights enablers of new genomics applications
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Health Care Leaders to Speak at BaseSpace® Suite Summit
Industry experts explore bioinformatics solutions that address genomic data analysis, management and interpretation
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Genomics and Health Leaders Address Precision Medicine
PMI Leaders Summit brings together leading physicians, patient advocates, and life science executives
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Illumina Accelerator Welcomes First International Fellow
Center of Individualized Diagnostic is focused on bringing genomic diagnostics to Saudi Arabia
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Illumina Introduces Bovine Parentage Sequencing Panel
Product Launched at International Society for Animal Genetics 2016 Conference
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HiSeq X® Debuts at the Science Museum, London
Our Lives in Data exhibition highlights the technology revolution that will impact our lives
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Reanalysis of CARE Study Shows Reduced NIPT False-Positives
Letter Published in the New England Journal of Medicine
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视频：与 Illumina 总裁兼首席执行官的一段对话
Francis deSouza reveals his motivations, inspirations and what's next at Illumina
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Backgrounder: The Many Facets of Microbial Genomics
Diverse markets share common focus on improving human health and safety
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Illumina Launches Propel Certification Program for Core Labs
New program promotes data quality and best practices at Illumina-powered fee-for-service laboratories
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MiniSeq Data to Inform Breast Cancer Research in Ireland
Go Mini Scientific Challenge Winner Una McVeigh Excited to Gain Experience with NGS
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VIDEO: One Couple’s Struggle with Infertility
April 24-30 is National Infertility Awareness Week
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Noninvasive Prenatal Testing Recommended for All Pregnancies
ACOG and SMFM issue joint bulletin updating guidance from 2007 to include NIPT for all pregnant women
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Noninvasive Prenatal Testing Recommended for All Pregnancies
ACOG and SMFM issue joint bulletin updating guidance from 2007 to recommend NIPT for all pregnant women
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Jay T. Flatley: 17 Years of Leadership
Infographic provides an overview of Illumina’s remarkable growth 1999-present
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Southern California Becoming Hub for Rare Disease Research
Thought leaders, philanthropy, and patient advocates have strengthened the local rare disease community
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Mapping Neural Diversity in the Mouse Visual System
Non-profit research organization using single-cell sequencing to understand how the brain works
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NGS Provides Promise in Microbiology
New American Academy of Microbiology paper highlights important considerations for the field
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‘Lucky’ Endangered Fish Gets Sequenced
Prized commercial fish sheds light on evolutionary history; offers hope to conservationists
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Scientific Voyage Provides Insights into Ocean Ecology
Four-year expedition sent more than 200 scientists onto the open seas to map ocean biodiversity
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Growth in Americas Driven by Sequencing, Clinical Markets
Mark Van Oene, VP and General Manager of Americas for Illumina, shares insights for the year ahead
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Largest Shared Genomic Database for Autism to Be Established
BaseSpace® Cloud enables quick analysis of genomic information to advance treatment and therapies
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Oregon State University to Sequence Mascot’s DNA
University Researchers Seek to Better Understand American Beaver through Study of its Genome
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Illumina’s Evolving Array Portfolio
Illumina’s Senior Director of Product Marketing discusses arrays as an integral part of the company’s business
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Genome Sequencing Solves Ebola Mystery
NGS shows barely detectable virus is responsible for the death of a woman
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VIDEO: 10 Years of Infinium Array-Powered Progress
Celebrating the last decade of Illumina arrays
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Educating Patients and Providers on Prenatal Genetic Testing
Illumina supports non-profit organization to help provide educational resources and establish patient registry
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Pioneering Pre-implantation Genetics
Physician at Melbourne IVF co-developed key methods for successful IVF pregnancies
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VIDEO: Non-Invasive Prenatal Testing in Practice
Interview with Dr. Martin Chavez, Chief of Maternal Fetal Medicine & Fetal Surgery at Winthrop University Hospital
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VIDEO: Spontaneous Remission of a Genetic Syndrome?
Whole genome sequencing clears up medical mystery
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Irish Cattle Breeding Federation Selects Illumina
One million samples to be tested for genome program
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Leading the Charge in Genetic Counseling
An interview with Illumina’s Staff Genetic Counselor, Erica Ramos
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Telling the Difference Between Identical Twins
Whole genome sequencing goes beyond standard paternity, forensic testing methods
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Illumina Accelerator Graduates its First Genomics Startups
Founders share their experiences and what’s next
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Smart Screening Increases Successful IVF Pregnancies
Assessing the genetic viability of embryos
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Seeking the origins of Alzheimers and Dementia
Researchers are turning to genomic technologies to peer into the epigenome
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Unlocking Secrets of Cancer and Autoimmune Diseases
Research at Icahn School of Medicine shows how genetic changes in RNA and DNA drive specific biological subsystems
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Illumina Completes Expansion in Madison
Features fermentation suite, expands life science community
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Mummified Remains Yield 14 TB Strains
Deep sequencing allows for multi-strain detection in Hungarian specimens
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Genomics on Its Way to Becoming Pervasive
Applications of next-generation sequencing are far-ranging
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NGS Aids Researchers in the Ebola Fight
Genomic studies are enabling researchers to track outbreaks and understand the virus’s rapid mutation rate
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Backgrounder: The Agrigenomics Market
How researchers, breeders, and farms are using genomics to improve global food security
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How Exercise Impacts Our DNA
How endurance training makes epigenetic changes to the human genome
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Exploring Memories and the Brain
Using sequencing, crowd-sourcing and the internet to research memory and learning
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Illumina Scales for Growth in China
Tim Orpin on the company’s strategy to address the world’s largest NGS market
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Research & Clinical Sequencing Services
Whole genome sequencing for research or the clinic are different, but both are about improving human health
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Connecting the Continuum in Reproductive and Genetic Health
NextSeq 550 merges next-generation sequencing and microarray scanning for one comprehensive solution
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What’s Next for NGS Regulation?
Illumina’s VP of Regulatory Affairs on the company’s updated strategy
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White House Calls for New Era of Precision Medicine
Genome sequencing to aid in finding more effective treatment for disease
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DNA Sequencing Used to Study Changes in Gut Microbiome
Researchers use Illumina systems to trace microbiota restoration after Clostridium difficile infection
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Illumina’s Life Sciences Business Poised for Growth
Kirk Malloy, Senior Vice President and General Manager, talks about the year ahead
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Rare Gene Variant Could Protect Against Heart Attacks
Combination of sample access and analysis methods sheds light on association between genes and disease
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Alex Dickinson Talks ‘The End of Disease’ (video)
Covers vision for future of genomics at TEDx Orange Coast
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