272 Results
Article Type
Introducing the Illumina–University of Melbourne Genomics Hub
Positioning Australia at the forefront of healthcare innovation
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NextSeq 550Dx Approved for Clinical Use in China
Continued expansion of clinical products further advances precision medicine globally
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Transforming Diagnoses and Care for Acute Myeloid Leukemia
Illumina supports program to bring NGS technology to Latin America
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The New Workflow: How Labs Will Benefit from TSO 500 Updates
Innovative enhancements streamline enablement of in-house comprehensive genomic profiling
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Accelerating Genomics: Astarte Medical Launches NICUtrition®
Illumina Accelerator graduate’s platform addresses unmet needs in neonatal intensive care
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Illumina Pledges US $20 Million in Sequencing Tech for Africa
Joins Africa CDC alongside the Bill & Melinda Gates Foundation and others in a four-year plan
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Fighting For My Life, I Also Fought For Yours
By: Sandra Balladares, Ph.D., Global Marketing Manager at Illumina
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DRAGEN Shines at PrecisionFDA Truth Challenge
Illumina sequencing and software analysis are best in class for accuracy
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Supporting Climate Action
Integrating sustainable solutions across facilities, products and business practices
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Ancient DNA Reveals the Truth About the Vikings
A new study uses NGS to unlock surprising genomic secrets from Norse civilization
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Australia Creates First National COVID-19 Tracking System
Initiative uses Illumina sequencing technology to understand transmission and spread of the virus
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Illumina-led Research Team Identifies Preeclampsia Biomarkers
Circulating RNA has tremendous potential to drive early diagnoses
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DNA Tandem Repeats Implicated in ASD
Illumina technology plays role in unique population study
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Illumina and SPHCC Accelerate NGS Research in Shanghai
Leading institute will implement our technology and training with goal of epidemic prevention
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54gene Uses Illumina Sequencing to Create World-Class Facility
Partnership focuses on leveraging the diverse African genome to improve healthcare
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Illumina’s COVID Testing Service
New program leverages NGS-based diagnostics to scale up testing in the U.S.
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Illumina Reaches Milestone with 1,000 NovaSeq 6000
Three years after its debut, NovaSeq makes deeper discoveries more accessible than ever
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COVIDSeq Test Expands to More Customers
FDA amendment leverages the power of various Illumina sequencers for COVID-19 testing
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New Guidelines Recommend Non-Invasive Prenatal Testing for All
Endorsement from ACOG opens doors for pregnant women of any age or risk
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Empowering India’s Frontline COVID-19 Testing with COVIDSeq™
Leveraging next-generation sequencing to detect COVID-19
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Ensuring Access to Genetic Testing
New report investigates barriers, proposes solutions
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Minutes Matter. New PCR-Free Prep Expedites Whole-Genome Sequencing
New library prep kits enhance research in rare genetic diseases
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Illumina Acquires Enancio’s Compression Software
Reduces genomic data storage and transfer costs associated with the data deluge
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Collaborative Environment Released for COVID-19 Host Response Research
Enables and accelerates research leveraging BaseSpace Correlation Engine
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New Hope for Rare Disease Families
TruSight Software Suite Accelerates the Identification of Genetic Diseases
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New Sustainable Packaging Arriving Now
Environmentally friendly packaging reduces waste from landfills and carbon emissions
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Introducing the Enhanced RNA-Seq Library Prep Product Portfolio
New solutions for studying RNA for infectious disease, oncology, and genetic disease research
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Burning Rock and Illumina Grow China Partnership
Extending next-generation sequencing technologies for cancer therapy selection
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Two Years In,DRAGEN Roars
Delivering accurate data with deeper insights to unlock new discoveries
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Illumina to Sequence Genomes for New UK-wide COVID-19 Study
Data from severely ill patients may help us understand the genetics of susceptibility
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TruSight Oncology Family Grows with Liquid Biopsy and High-Throughput Assays
Providing customers with a versatile, scalable, sample-to-report workflow
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Illumina Publishes First Corporate Social Responsibility Report
Our approach to global citizenship and environmental stewardship has never been more relevant or important
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Illumina and IDbyDNA Partner to Deliver NGS Infectious Disease Solutions
Partnership aims to accelerate NGS adoption for clinical infectious disease testing
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Illumina Perspective on the Novel Coronavirus SARS-CoV-2 (2019-nCoV) Outbreak:
What We Know Today and Where Do We Go from Here
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Patients With Challenging Cancers to Benefit from Genomic Sequencing
University of Melbourne and Illumina Target Diagnosis of Difficult Cancers
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Next-Generation Sequencing Helps Fight Infectious Diseases Globally
Case in Point: The Novel Coronavirus
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Illumina Sequencers Help Characterize and Control Coronavirus
NGS Accelerating Viral Identification and Control Measures
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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 Announces the Twelfth Agricultural Greater Good Grant Winner
International Mungbean Improvement Network Wins Grant
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Illumina Registers MiSeqDx Instrument in Japan
Two Next-Generation Sequencers Now Available for In Vitro Diagnostics
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Australia Launches Genomics Program for Indigenous People
First Event of its Kind Aims to Build Network of Indigenous Genomics Professionals
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CEO Francis deSouza Speaks at HLTH 2019
Discusses transformational power of genomics and how to bring its benefits to more people, faster
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Autumn Analyzed
Transcriptome research is helping us understand the biology of the changing world
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New Liquid Biopsy and High-Throughput Assays Join TruSight Oncology Portfolio
Provides customers the capability to run blood and tissue samples on the NovaSeq 6000 Sequencing System
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Texas A&M Deploys DRAGEN
First American Academic Institution Install for Agricultural Applications
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Illumina Accelerator Turns Five and Backs Five New Startups
Celebrates Continued Achievements by Inaugural Funding Cycle; Invests in Five New Companies for Tenth Cycle
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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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Illumina’s Global Diversity Array Now Available
Array Delivers More Informative Content for Ethnically Diverse Population Genomics Programs
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Illumina Foundation and Discovery Education Launch New DNA Decoded Resources
Helping Students Nationwide Learn the Real-World Impacts of Genomics
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Sustainable Efforts Reduce Illumina’s Environmental Footprint
The New Fuel Cell Power Generation System is the Largest in San Diego
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Every Diagnosis Matters
Families facing rare diseases often spend years pinpointing the problem in solitude – until now
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What Nobel Laureate, Frances Arnold, Wants Future STEM Leaders to Know
From Genomics to STEM Education, the Modern-Day Darwin Leaves No Topic Unturned
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Earth BioGenome Project Builds Foundation to Sequence Life
Illumina to contribute complementary short-read data
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CEO Francis deSouza Speaks at Aspen Ideas: Health
Shares views on actions needed to bring genomics to the patients who need it
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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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Chinese Collaboration to Develop Cancer Tests on Illumina System
AnchorDx to focus on early cancer detection and clinical management panels
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Driving Insights Through Microbiome Profiling
Metagenomic Shotgun Sequencing Workflow Enables Accurate DNA Detection From Soil
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European Customers Share Their Genomics Stories
Illumina at the 52nd Annual European Society of Human Genetics
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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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Progress for Patients with Rare and Undiagnosed Genetic Diseases
Evidence Street® issues review supporting Whole Genome Sequencing
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Knowledge is Power: Unlocking the Potential of the Genome
New survey finds Americans unaware of DNA's power to improve lives
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Illumina Accelerator Invests in Four Startups for Ninth Cycle
Graduate Companies Have Raised $190 million in Funding from Leading Life Science and Tech Investors
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Illumina and China's Children’s Hospital of Fudan Bring Rapid WGS to the NICU
This collaboration is the first to introduce the concept of rWGS in China for indiscriminate detection in the NICU
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Cambridge Science Festival Sparks Scientific Enthusiasm
Illumina Foundation extends global support of STEM efforts.
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A Snapshot Into the Past
The Mysteries Hidden within Ancient DNA May Harness the Answers to Today’s Mental Health Epidemic
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How Diversity in Science Can Benefit Communities
Illumina Researcher Marlem Rivera Shares Her Story
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Genetic Kidney Diseases are Focus of New Partnership in China
Illumina and BOAI NKY Develop Next Generation Sequencing for Chinese NMPA
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Leading Health and Research Organizations Launch the Medical Genome Initiative
Consortium aims to expand access to high-quality clinical whole genome sequencing for genetic diseases
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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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Francis deSouza Speaks at the 16th Annual Precision Medicine World Conference
A discussion about the current and future state of genomics with Twist Bioscience’s Emily Leproust
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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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NovaSeq™ 6000 S Prime Reagent Kits Now Available
100-, 300- and 500-Cycle Kits expand the flexibility of the most powerful sequencer from Illumina
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Careers of the Future – An Illumina Spotlight Series
Get to Know Alicia Scocchia, Genetic Counselor
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The FDA Grants Breakthrough Device Designation for Illumina’s TruSight Assay
Based on the content of TruSight Oncology 500, the proposed in vitro diagnostic will receive prioritized review and resources
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Illumina Releases SpliceAI, Open Source AI software for Interpretation
SpliceAI interprets noncoding mutations in rare and undiagnosed diseases
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TruSight Oncology 500 Selected to Power Liquid Biopsy Studies
Illumina to collaborate with the Frederick National Laboratory for Cancer Research
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Illumina Announces Eleventh Agricultural Greater Good Initiative Grant Winner
Recipient Focused on Genetics Research of Camels
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TruSight Oncology 500: The Unifying Force has Arrived
Offering deep, comprehensive and accessible sequencing power for detecting solid tumor biomarkers
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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 Erin Fang, Bioengineer
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Landmark 100,000th Genomes Project Reaches Milestone
Illumina sequences 100,000th genome in partnership with Genomics England and NHS
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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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Veterans Helping Veterans Conquer the 'Invisible Wound'
TruGenomix Health is Leveraging Genomics to Battle Post Traumatic Stress Disorder
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Illumina Partners with Blue Cross Blue Shield Association
Project to focus on genetic testing technologies to expand access to personalized medicine
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Oncology: Restoring Order from Disorder
By: Phil Febbo, M.D., Chief Medical Officer of Illumina
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The Power and Portability of the iSeq
Empowering the capabilities of Illumina’s smallest sequencer in the Democratic Republic of the Congo
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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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Illumina Accelerator Announces Eighth Investment Cycle
Five new genomics startups focused on therapeutics, diagnostics and informatics
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Bottlenose Dolphin Genome Made Available to Researchers
Facilitates research on comparative genomics, provides structure for cataloging biodiversity
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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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Illumina Releases Open Source AI Software
Streamlines genome interpretation to improve the utility of genomic data
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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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What is Your Gut Telling You?
NGS-based microbiome profiling delivers enhanced insights for metagenomics studies
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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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2020 Vision for Genomics
Looking forward, Dr. Eric Green talks to Illumina about the future of genomics
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CEO Francis deSouza's Conversation at CodeCon
Decoding Illumina for the Digital and Tech Community
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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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The Art of Celebrating Illumina's 20th Anniversary
San Diego artist dedicates painting in honor of science and innovation
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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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Illumina Accelerator Invests in Five New Genomics Startups
Seventh funding cycle companies focused on therapeutics, fertility and data science
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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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WeGene Announces Collaboration with Illumina to Serve Asia Market
WeGene Selects Illumina’s microarrays for a new laboratory in Asia.
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WGS Will ‘Transform the Research Landscape for Diseases’
UK Biobank Enters Exciting New Phase of Genetics Research
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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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Adventures in Genomics: The Fight Against Ebola
Arming the outposts in the 2014 Ebola outbreak
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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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Illumina Launches Its BaseSpace™ Sequence Hub in China
Providing powerful genetic data storage, analysis, and collaboration to thriving Chinese market
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Jay Flatley’s Award-winning Year
Illumina’s Executive Chairman honored at three events in 2017
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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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Illumina Introduces Nextera DNA Flex
A Next Generation Technology for Whole Genome Sequencing Applications and More
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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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Illumina Accelerator Introduces Sixth Cycle of Startups
Genomic companies focused on drug discovery, advanced materials and digital health
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Resilient Biotics is on a Microbiome Therapeutic Crusade
Illumina Accelerator Graduate Takes on Antibiotic Use in Livestock
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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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New panel helps researchers study neurodegenerative diseases
Researchers hope to shed light on genes associated with neurodegenerative conditions like Alzheimer’s disease
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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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MetaSUB - Molecular Portraits of World Cities
Using NGS to map Stockholm’s subway microbiome
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Illumina and ASCO Jointly Donate to CIViC Database
Sharing genomic insights to help improve cancer treatment and outcomes
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Genomics Powering Access to the Latest Cancer Breakthroughs
An interview with Garret Hampton, EVP Clinical Genomics Group at Illumina
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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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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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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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Illumina Executives Forge Key Genomic Relationships in China
Meetings highlight shared genomic interest, innovation and technology
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SeqGeqTM Single Cell Data Analysis Software Available Now
Collaboration between FlowJo, LLC and Illumina yields tool for understanding single cell NGS data
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Celebrating DNA Day
Illumina’s head of Scientific Affairs, Jacques Retief, shares his perspective on recent scientific breakthroughs
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Individual Lane Loading in Development for NovaSeq Series
Optional workflow will allow laboratories to load sequencing libraries into individual flow cell lanes
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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
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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Seafood Offers Opportunity to Feed Growing Human Population
Illumina genomics tools can be used to improve fisheries and seafood production
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Illumina Accelerator Graduate Xcell Bio is Making Big Moves
CEO Brian Feth discusses the company’s journey after Illumina Accelerator
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Illumina, IMPLAD to Establish Reference for Chinese Medicine
First Genomic Reference for 1,000 Traditional Medicinal Plants to Standardize Chinese Pharmacopeia
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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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Illumina Accelerator Welcomes its Fifth Cycle of Startups
Genomic companies developing microbiome and small molecule treatments
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David Cameron Visits Illumina, Discusses Genomics
Former Prime Minister of the United Kingdom Reflects on Genomics England Project
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Illumina Inducted into U.S. SBA Hall of Fame
Lifetime Achievement in Innovation Research and Extraordinary Success
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Sweet Potato Sequencing Effort Aims to Improve Food Security
G. Craig Yencho and Bode Olukolu Win 2017 Agricultural Greater Good Initiative Grant
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Illumina, Children’s Hospital of Philadelphia Launch Study
LeukoSEQ to study sequencing as diagnostic tool for rare diseases
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Meet the NovaSeq™ Series
Illumina’s Newest High Throughput Sequencing Instrument Debuts at J.P. Morgan
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2016 Wrap-up: The Top 10 Stories of the Year
A look back at Illumina’s year in the news
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Customer Focus on Edinburgh Genomics
Scottish partnership paving the way to advances in research and personalized medicine
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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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ALS Ice Bucket Challenge Two Years On
How ProjectMinE is making new discoveries using Illumina’s whole genome sequencing
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UK Prime Minister Opens Hinxton Facility
Ceremony celebrates Illumina and 100,000 Genomes Project partnership
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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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Queen Starts Illumina Genome Sequence
$800m Francis Crick Institute Official Royal Opening
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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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Indian Prime Minister Recognizes Scientist’s NGS Work
Dr. Rajeev Varshney honored for work completing genome sequences of agriculturally important crops in India
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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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DKFZ - Research for a Life Without Cancer
Two leading experts discuss the impact of next-generation sequencing in Germany
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DNA Sequencing on Display
The Field Museum Uses DNA to Explore the Biodiversity on Earth
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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 Program Aims to Improve Global Food Security
Agricultural Greater Good Initiative Applications Now Open
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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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A Conversation with Illumina's President and CEO
Francis deSouza reveals his motivations, inspirations and what's next at Illumina
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Illumina Dedicates Jay T. Flatley Innovation Center
New Innovation Gallery offers a look back at Illumina’s history and longtime CEO’s legacy
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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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Illumina Registers MiSeqDx System in Australia
Product is now available for clinical use on five continents
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Smart Tampon Technology: The Future of Reproductive Health
A Q&A with the founders of Illumina Accelerator startup, NextGen Jane
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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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One Couple’s Struggle with Infertility
April 24-30 is National Infertility Awareness Week
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How Genomics is Shaping the Future of Oncology
An interview with John Leite, VP of Marketing for Illumina’s Oncology business
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Illumina Announces Winners of Go Mini Scientific Challenge
Winning laboratories to use next-generation sequencing for entomology, virology, and oncology research
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The Genetics Behind Language and Reading Disorders
A Yale laboratory is studying genetic variants associated with developmental disorders
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BaseSpace Suite Wins People’s Choice at Bio-IT World
Newly introduced genomics software solution voted Best of Show by industry participants
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Using Songbirds to Study Neurobiology of Vocal Communication
Researchers at Duke University Medical Center are studying songbird genomes for clues about human vocal learning
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Big Data Meets Big Biology
Xconomy event highlights data considerations as the applications of genomics grow
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Illumina Unveils New Customer Training Labs in EMEA
State-of-the-art facility enables customers to maximize Illumina’s broad product portfolio
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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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Integrating Clinical Genome & Exome Sequencing into Medicine
Multidisciplinary experts publish comprehensive recommendations
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Southern California Becoming Hub for Rare Disease Community
Thought leaders, philanthropy, and patient advocates have strengthened the local 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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Illumina Acquires Conexio Genomics
Acquisition strengthens company’s ability to deliver sample-to-report solutions for HLA typing
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VIDEO: Experts Weigh In from Festival of Genomics, London
Genomics England, Illumina leaders explain how genomics will revolutionize healthcare
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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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Live from J.P. Morgan: Genomics Everywhere
A wrap-up of the news from Illumina President Francis deSouza
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Illumina Breaks Ground on New Facility in Foster City
Local and state representatives gather to commemorate the ceremony
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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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From Conception to Birth and Beyond
Illumina’s Reproductive and Genetic Health business is growing with solutions that span the complete continuum
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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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10 Years of Infinium Array-Powered Progress
Celebrating the last decade of Illumina arrays
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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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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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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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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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Separating Fact From Fiction About Infertility
Genomics can help improve the possibility of having a live birth
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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’
Covers vision for future of genomics at TEDx Orange Coast
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