GeneTiCA Kft | Get-to-know

It’s all about accessibility: Developing technical training for the MiSeq i100

Read more

Hírek

14. 05. 2025 - Illumina DRAGEN v4.4 powers clinical oncology research and multiomic applications

12. 05. 2025 - In May 2025, Illumina will be hosting the 6th edition of “Epigenetics: the full picture” – a virtual event dedicated entirely to epigenetics

05. 05. 2025 - Illumina FFPE DNA Prep with Exome 2.5 Enrichment - a fast, flexible, and scalable human whole-exome sequencing solution with support for low-input samples

02. 05. 2025 - Illumina and Ovation.io launching first-of-kind GLP-1 dataset to accelerate new therapy development

30. 04. 2025 - The rare disease community fights for precision medicine, from diagnosis to cure

23. 04. 2025 - WEBINAR: Metagenomics: Introduction to library preparation and sequencing

22. 04. 2025 - Multiomics Newsletter Illumina

14. 04. 2025 - More single-cell data, less equipment – A new Illumina solution for every lab

07. 04. 2025 - Don't miss out on All Things Multiomics

02. 04. 2025 - How Illumina designs a gene sequencer

26. 03. 2025 - WEBINAR: Advancing Food Safety Testing with Next Generation Sequencing (NGS) and Illumina

24. 03. 2025 - WEBINAR: How Can AI and Automation Boost Cytogenetic Array Analysis Efficiencies?

23. 03. 2025 - Your guide to genomic innovation: The Illumina Roadmap

20. 03. 2025 - Alliance for Genomic Discovery completes 250,000 whole genomes to accelerate drug discovery

19. 03. 2025 - WEBINAR: GenomeStudio - Creating Custom Cluster Files

17. 03. 2025 - WEBINAR: Unlocking the Epigenome: Advances in Methylation Arrays for Cancer Research

10. 03. 2025 - Unlocking precision medicine in sarcoma care: The role of whole-genome and whole-transcriptome sequencing

07. 03. 2025 - Illumina named to Dow Jones Best-in-Class Indices for sixth consecutive year and as a Sustainability Yearbook Member for fourth consecutive year

06. 03. 2025 - Constellation technology saves valuable time and unlocks a more complete genome

27. 02. 2025 - WEBINAR: How Can AI and Automation Boost Cytogenetic Array Analysis Efficiencies?

26. 02. 2025 - Illumina and Broad Clinical Labs usher in new era of drug discovery with collaboration to rapidly scale single-cell solutions

25. 02. 2025 - WEBINAR: Illumina’s Integrated Workflow for Rare and Undiagnosed Genetic Disease Research

24. 02. 2025 - Discover high-quality comprehensive genomic profiling. Now with faster sequencing times and improved economics with the NovaSeq X Series, NextSeq 1000 and NextSeq 2000.

21. 02. 2025 - Illumina unveils first-of-its-kind spatial transcriptomics technology

20. 02. 2025 - Illumina To Webcast Upcoming Investor Session at the Advances in Genome Biology and Technology (AGBT) Conference

17. 02. 2025 - Illumina Innovation Roadmap: ASHG Industry Education session

11. 02. 2025 - Introducing constellation mapped read technology

10. 02. 2025 - WEBINAR: More single-cell data, less equipment – A new Illumina solution for every lab

04. 02. 2025 - Inside the new Illumina MiSeq i100 Series: The making of the software

03. 02. 2025 - Listen to the presentations from Illumina’s ESHG 2024 workshop. Prof. Dr. Malte Spielmann, shared his first-hand experience of implementing Genome sequencing in the clinic

28. 01. 2025 - VIDEO: The first NovaSeq X in the Benelux region is a “game changer”

27. 01. 2025 - More to see with Liquid Biopsy

21. 01. 2025 - If there is a monster in Loch Ness, this geneticist will find it

20. 01. 2025 - Illumina Innovation: Bringing XLEAP-SBS Chemistry to NextSeq 1000 and 2000

16. 01. 2025 - Illumina and NVIDIA collaborate to decode biology and propel precision health

15. 01. 2025 - Illumina launches pilot proteomics program with UK Biobank and biopharma collaborators to analyze 50,000 samples

14. 01. 2025 - Studying epigenetics to avoid unwanted effects of blood transfusions

13. 01. 2025 - Pillar oncoReveal Liquid Biopsy panels

07. 01. 2025 - WEBINAR: MiSeq i100 Series empowers new sequencing possibilities

06. 01. 2025 - WEBINAR: Microbial Profiling – Harness the Potential of Metagenomics & Metatranscriptomics

27. 12. 2024 - WEBINAR: Learn more about how RNA sequencing is utilized in oncology, microbiology and genetic disease

27. 12. 2024 - Programs around the globe bring newborn screening into the Genome Era

19. 12. 2024 - Sustainable sequencing in the new MiSeq i100 Series

16. 12. 2024 - WEBINAR: One Health Genomic Surveillance Simplified Illumina Microbial Amplicon Prep

12. 12. 2024 - WEBINAR: Unlocking the Epigenome: Advances in Methylation Arrays for Cancer Research

09. 12. 2024 - New version alert: Emedgene V36, enabling streamlined variant interpretation for genetic disease research, is now available and more powerful than ever.

06. 12. 2024 - WEBINAR: Streamlining data analysis of genomes and exomes in oncology clinical research

04. 12. 2024 - WEBINAR: DRAGEN Command line for Beginners

11. 11. 2024 - The emerging population genomics revolution

04. 11. 2024 - Zurich lab imagines new possibilities in microbial research and diagnostics

01. 11. 2024 - Illumina to preview newest innovations in NGS and multiomic technologies at the American Society of Human Genetics Annual Meeting

29. 10. 2024 - On a mission to help oncologists diagnose a mysterious, aggressive cancer

24. 10. 2024 - WEBINAR: For All You Seq: Benchtop sequencing applications

14. 10. 2024 - “Genomic testing saved my life”

14. 10. 2024 - “Genomic testing saved my life”

10. 10. 2024 - WEBINAR: Discover what's possible with XLEAP-SBS chemistry

07. 10. 2024 - Pursuing precision oncology with world-class custom bioinformatic pipelines

30. 09. 2024 - The only NGS benchtop with fully automated FASTQ file generation and secondary analysis included

25. 09. 2024 - FDA Approves TruSight Oncology Comprehensive Assay As Pan-Tumor Companion Diagnostic

24. 09. 2024 - VIDEO: Highlighting the role of CGP in cancer treatment at ESMO 2024

23. 09. 2024 - Illumina launches the XLEAP-SBS P1, P2, and P3 Reagent Kits – officially completing the family of XLEAP-SBS reagents on the NextSeq 1000/2000

17. 09. 2024 - In Edinburgh, taking comprehensive genomic profiling to the next level

12. 09. 2024 - For the first time ever, gene expression can be mapped from space

10. 09. 2024 - Podcast stories explore unusual and surprising applications of genomics

09. 09. 2024 - Transform Oncology with Genomics - Illumina will be at ESMO 2024

02. 09. 2024 - Data Analytics Boosting Next-Gen Sequencing Methodologies

02. 09. 2024 - Evolving threats require evolving solutions

27. 08. 2024 - FDA approves Illumina cancer biomarker test with two companion diagnostics to rapidly match patients to targeted therapies

19. 08. 2024 - PODCAST: Gene expression reveals early warning signs of cancer and aging

14. 08. 2024 - Illumina announces strategy to accelerate value creation

13. 08. 2024 - Searching for unique biomarkers that make local cattle breeds more resilient

12. 08. 2024 - Illumina Cell-Free DNA Prep with Enrichment

07. 08. 2024 - Delivering hope for parents and critically ill newborns

06. 08. 2024 - Illumina launches new oncology menu for NovaSeq X Series customers

05. 08. 2024 - The NovaSeq X Series and 25B flow cell are ready to take your projects to the next level

30. 07. 2024 - Australia’s latest research investment in improving generational health

29. 07. 2024 - Educational eBooks: Evolving threats require evolving solutions

23. 07. 2024 - Sequencing Benefits Even Low-Income Rare Disease Patients, iHope Study Shows

22. 07. 2024 - WEBINAR: Unlock the Power of Precision Medicine with PGx Star Allele Calling

16. 07. 2024 - Illumina helps pioneering health systems deliver precision medicine

15. 07. 2024 - Multiomics: an integrated approach to power discovery

11. 07. 2024 - Illumina acquires Fluent BioSciences to accelerate single-cell analysis and discovery to a broader customer base

09. 07. 2024 - Podcast stories explore unusual and surprising applications of genomics

08. 07. 2024 - Deciphering the Impact of Metagenomics in Human Disease

02. 07. 2024 - Missed opportunities for cancer patients

01. 07. 2024 - Precision Metagenomics ebook

26. 06. 2024 - WEBINAR: Illumina DRAGEN v4.3: Comprehensive coverage with leading edge innovations

26. 06. 2024 - WEBINAR: Illumina DRAGEN v4.3: Comprehensive coverage with leading edge innovations

24. 06. 2024 - VIDEO: Harnessing single-cell & spatial genomics for the Human Cell Atlas

17. 06. 2024 - WEBINAR: Expansive analysis of NGS data in solid cancer

13. 06. 2024 - WEBINAR: Simultaneous Profiling of the Epigenome and Transcriptome at a Single Cell Level

12. 06. 2024 - Illumina DRAGEN v4.3 powers most comprehensive, accurate genome with industry-leading innovations

09. 06. 2024 - Watch the on-demand recordings of 2024 Epigenetics – the full picture virtual event to discover recent epigenetic studies and breakthroughs concerning human health, disease, and agrigenomics.

05. 06. 2024 - Illumina launches latest chemistry across most popular mid-throughput sequencers, enabling higher quality and greater speed for customers at lower cost

04. 06. 2024 - In Brazil, building genomic evidence for a better tomorrow

03. 06. 2024 - Visit Illumina Liquid Biopsy On-demand Webinars

30. 05. 2024 - Illumina drives genomic testing as standard of care in oncology through collaborative research presented at ASCO

29. 05. 2024 - Illumina releases 2023 Corporate Social Responsibility Report

28. 05. 2024 - FDA approves OncoReveal CDx on Illumina MiSeq Dx system

27. 05. 2024 - Precision Metagenomics ebook

20. 05. 2024 - WEBINAR: Illumina Innovation: Bringing XLEAP-SBS Chemistry to NextSeq 1000 and 2000

14. 05. 2024 - Podcast stories explore unusual and surprising applications of genomics

13. 05. 2024 - Next-Generation Sequencing (NGS) is a powerful tool for answering your research questions, and it's easier than you think.

07. 05. 2024 - Inspiring young minds: HRH The Princess Royal helps Illumina celebrate DNA Day

06. 05. 2024 - VIDEO: An IVDR-compliant clinical genomic assay

02. 05. 2024 - NextSeq 2000 customer story

01. 05. 2024 - Evidence supports sequencing as first-line rare disease diagnostic

29. 04. 2024 - Illumina makes it easier for clinical labs to unlock the power of the human genome

23. 04. 2024 - PODCAST: Genomic AI millions of years in the making

22. 04. 2024 - Comprehensive Genomic Profliling (CGP) can identify more clinically relevant alterations than conventional testing approaches, such as single-gene tests and small targeted panels

16. 04. 2024 - Why more clinical labs are turning to whole-genome sequencing for cancer

15. 04. 2024 - Epigenetics: the full picture

09. 04. 2024 - DRAGEN takes the mystery out of cardiovascular disease

08. 04. 2024 - Uncover more with whole-genome sequencing

02. 04. 2024 - Illumina cell-free DNA Prep with Enrichment

26. 03. 2024 - PODCAST: The Genome Era demands accessibility and integration

25. 03. 2024 - eBook: Unlock the next wave of genomic discovery with NovaSeq X Series

19. 03. 2024 - Researchers harness the power of the Illumina Correlation Engine

18. 03. 2024 - Revealing the most challenging regions of the genome

12. 03. 2024 - Finding the needle in the genomic haystack with DRAGEN

11. 03. 2024 - WEBINAR: Why should you prefer an IVDR certified NIPT test for your patients?

05. 03. 2024 - Reaching new heights in data quality and throughput on a benchtop sequencer

04. 03. 2024 - Enabling Precision Medicine in Oncology

21. 02. 2024 - WEBINAR: Generation of real-world single cell data through a CAP accredited lens

14. 02. 2024 - WEBINAR: Panel Discussion on Getting Started with NGS

07. 02. 2024 - VIDEO: Inside the UK’s largest life sciences event

06. 02. 2024 - Inexpensive Sequencing Is Enabling the Age of Multiomics

05. 02. 2024 - We are prepared for the IVDR transition – are you?

31. 01. 2024 - Liquid biopsy can help overcome the potential limitations of tissue biopsies and assure biomarker testing for all cancer patients

30. 01. 2024 - Move Beyond Traditional Methods

29. 01. 2024 - Pioneering Genomic Progress: An Interview with Rami Mehio, Illumina's Software and Informatics Expert

25. 01. 2024 - TruSight Oncology 500 ctDNA v2 is now available! Next version comprehensive genomic profiling (CGP) from liquid biopsy (blood) offers higher analytical sensitivity from lower cfDNA input

23. 01. 2024 - What 5000 ancient human genomes can reveal about European health and heritage

22. 01. 2024 - WEBINAR: Exploring Microbiomes and Cancer Immunology

17. 01. 2024 - VIDEO: Enabling CGP from Liquid Biopsy with TruSight Oncology 500 ctDNA v2

16. 01. 2024 - What happens when a virus becomes a permanent part of your genome?

10. 01. 2024 - Blazing the trail to empower agrigenomics research and conservation

09. 01. 2024 - Illumina expands collaboration with Janssen to advance molecular residual disease cancer test

04. 01. 2024 - The Alliance for Genomic Discovery welcomes Bristol Myers Squibb, GSK, and Novo Nordisk

02. 01. 2024 - Nucleus Genomics wants to make personalized health care a reality

31. 12. 2023 - Agrigenomics Genotyping Arrays Portfolio (PDF)

31. 12. 2023 - NextSeq 1000 & NextSeq 2000 Sequencing Systems (PDF)

21. 12. 2023 - Move Beyond Traditional Methods

19. 12. 2023 - VIDEO: Merging discovery with clinical care at Ontario Institute for Cancer Research

18. 12. 2023 - DNA methylation studies to uncover new insights in human disease

12. 12. 2023 - How the UK is setting new standards for genomic research and better health care

11. 12. 2023 - Speed, scale and discovery power with NovaSeq X Series

06. 12. 2023 - Shriners Children’s big bet on the future of specialized pediatric care

05. 12. 2023 - WEBINAR: Wellcome Sanger Institute evaluation of Illumina Complete Long Reads

28. 11. 2023 - Preventing postoperative infections one NGS assay at a time

27. 11. 2023 - Targeted panels paint a partial picture. CGP completes the portrait.

22. 11. 2023 - EACR Industry Webinar with Illumina: New to NGS Live Panel Discussion

20. 11. 2023 - WEBINAR: Exploring Microbiomes and Cancer Immunology

13. 11. 2023 - Take your research higher with NGS - NEW Introduction to NGS eBook

07. 11. 2023 - VIDEO: Illumina highlights the importance of HRD testing at ESMO 2023

06. 11. 2023 - Recent genomic discoveries and advances

03. 11. 2023 - Illumina launches advanced liquid biopsy assay to enable comprehensive genomic profiling of solid tumors

31. 10. 2023 - VIDEO: Testing for NTRK fusions in solid tumors

30. 10. 2023 - Liquid Biopsy in Cancer Research eBook

24. 10. 2023 - What the diagnostic odyssey looks like—and how we can end it

23. 10. 2023 - What is Metatranscriptomics?

17. 10. 2023 - Q&A: An Illumina intern’s shift from academia to industry

16. 10. 2023 - The Polygenic Risk Score (PRS) Software Predict module and Infinium™ Global Diversity Array provides streamline genotype-to-risk prediction

11. 10. 2023 - It’s time to increase access to molecular testing for people with ovarian cancer

09. 10. 2023 - Achieve the next level of scale, cost efficiency, and sequencing capabilities with XLEAP-SBS coming in early 2024 - driving science forward faster than ever

06. 10. 2023 - Whole-genome sequencing (WGS) breaking frontiers on patient care

03. 10. 2023 - WEBINAR: Unlock the next wave of genomic discovery with NovaSeq X

26. 09. 2023 - Why pathogen surveillance is critical during a “tripledemic”

25. 09. 2023 - WEBINAR: Pathogen Genomics Surveillance with New Illumina panels

19. 09. 2023 - Insights from Dublin: Fostering precision oncology for better patient outcomes

18. 09. 2023 - The Greater Good Initiative rewards researchers like you, who are conducting ground-breaking research to improve sustainability and productivity of agricultural species

13. 09. 2023 - Illumina User Group Meeting – Boston (online option available)

11. 09. 2023 - European Congress of Pathology 2023 - No patient left behind: Importance of Comprehensive Genomic Profiling (CGP) and incorporating rare biomarkers into your practice (also available as on-demand)

07. 09. 2023 - WEBINAR: Live from the Customer Experience Lab in Amsterdam: GeoMx DSP from sample to data and more

06. 09. 2023 - Illumina User Group Meeting – Bay Area (online option available)

04. 09. 2023 - Recent genomic discoveries and advances

29. 08. 2023 - CGP in practice: growing utility and future perspective

28. 08. 2023 - Microbial Profiling – Harness the Potential of Metagenomics & Metatranscriptomics

23. 08. 2023 - Budi Hermawan’s long fight against tuberculosis

21. 08. 2023 - WEBINAR: Seq&Treat - enabling targeted NGS for detection of drug-resistant tuberculosis

15. 08. 2023 - How genetic technologies can empower more people with information

14. 08. 2023 - WEBINAR: Environmental DNA for biomonitoring of aquatic ecosystems

09. 08. 2023 - New research shows CGP is most effective as a standalone test

07. 08. 2023 - Prospective study supports use of WGTS in routine diagnostics of bone and soft tissue tumors

01. 08. 2023 - WEBINAR: Wellcome Sanger Institute evaluation of Illumina Complete Long Reads

31. 07. 2023 - What is Metatranscriptomics?

26. 07. 2023 - New AI tool searches genetic haystacks to find disease-causing variants

24. 07. 2023 - WEBINARS: RNA Sequencing: From Data to Insights

20. 07. 2023 - The Alliance for Genomic Discovery announces founding biopharma members: AbbVie, Amgen, AstraZeneca, Bayer, and Merck

18. 07. 2023 - Hundreds of new primate genomes offer window into human health—and our past

17. 07. 2023 - Illumina Complete Long Reads software analysis workflow for human WGS

14. 07. 2023 - Illumina DRAGEN 4.2 delivers most accurate and comprehensive coverage of the genome, powering greater applications and discovery

11. 07. 2023 - A liquid biopsy study offers new hope for lung cancer patients

10. 07. 2023 - Customer Experience with the NextSeq 2000

04. 07. 2023 - Addressing the genomics education gap

03. 07. 2023 - NextSeq 1000 and 2000: Product updates and key applications

27. 06. 2023 - Highlights from Glasgow: Educating and promoting the impact of WGS

26. 06. 2023 - Genomics in medicine - Xpeer

20. 06. 2023 - CGP validated in triple-negative breast cancer patients

19. 06. 2023 - Customer Experience with the NextSeq 2000

13. 06. 2023 - WEBINAR: NextSeq 1000/2000: Longer reads and extended informatics

12. 06. 2023 - Whole-genome sequencing (WGS) breaking frontiers on patient care

05. 06. 2023 - We are prepared for the IVDR transition - are you?

02. 06. 2023 - Illumina unveils AI software to predict disease-causing genetic mutations in patients

01. 06. 2023 - Real-world study data reveals better outcomes for cancer patients who receive comprehensive genomic testing

31. 05. 2023 - The future of precision metagenomics in treating infectious disease

29. 05. 2023 - VIDEO: Environmental DNA for biomonitoring of aquatic ecosystems

24. 05. 2023 - Illumina User Group Meeting – Toronto (an option to attend virtually)

22. 05. 2023 - WEBINAR: High throughput gene expression profiling with spatial resolution

17. 05. 2023 - Illumina's genomic technologies enable better pathogen preparedness and response

16. 05. 2023 - Illumina User Group Meeting – Houston (an option to attend virtually)

15. 05. 2023 - WEBINAR: Preventative Genomics: Future Impact on Healthcare

10. 05. 2023 - WEBINAR: Expand single cell possibilities with advanced chemistry for fresh or fixed samples

08. 05. 2023 - Genomic Sequencing for the next generation

04. 05. 2023 - WEBINAR: Experience the power of Xenium

04. 05. 2023 - VIDEO: Illumina Complete Long Reads

02. 05. 2023 - Illumina increases equitable access to STEM education, reaching over 1 million learners

28. 04. 2023 - WEBINAR: Revealing Illumina’s Innovation Updates

26. 04. 2023 - WEBINAR: Illumina User Group Meeting – Rockville

25. 04. 2023 - WEBINAR: We are prepared for the IVDR transition - are you?

20. 04. 2023 - Illumina celebrates 25 years of innovation

19. 04. 2023 - Rady’s Frontiers in Pediatric Genomic Medicine Conference 2023

18. 04. 2023 - 25 greatest impacts in 25 years: Illumina and the evolution of genomics

17. 04. 2023 - Revealing the most challenging regions of the genome

13. 04. 2023 - Illumina's cloud-based informatics programs recognized for robust, international data privacy protections

12. 04. 2023 - Illumina and Henry Ford Health team up to study impact of comprehensive genomic testing for cardiovascular patients

11. 04. 2023 - Illumina's revolutionary NovaSeq X exceeds 200th order milestone in first quarter 2023

11. 04. 2023 - WEBINAR: Epigenetics: the full picture

04. 04. 2023 - Illumina launches new software to enable tertiary analysis for oncology applications, and soon rare disease

03. 04. 2023 - Discoveries in Immunology at the single-cell level

29. 03. 2023 - VIDEO: What is homologous recombination deficiency (HRD)?

27. 03. 2023 - Using Single-Cell Sequencing to Investigate Murine COVID-19 Mortality

20. 03. 2023 - Illumina launches its first product enabling long- and short-read sequencing on one instrument

15. 03. 2023 - Children’s Mercy Kansas City tackles the unique complexity of pediatric cancer

13. 03. 2023 - Introducing the NovaSeq X and X Plus Sequencing Systems

13. 03. 2023 - Working to solve rare disease and support patients

07. 03. 2023 - Using whole-genome sequencing to study early-onset Parkinson’s disease

06. 03. 2023 - Illumina and Myriad Genetics expand partnership to broaden access to HRD testing in the United States

27. 02. 2023 - Find the next breakthrough cancer therapeutic with Visium

20. 02. 2023 - WEBINAR: Whole-Genome Sequencing and the way forward for Paediatrics

15. 02. 2023 - WEBINAR: NGS-Based Homologous Recombination Deficiency Assessment with a Semi-Automated Protocol

15. 02. 2023 - Illumina delivers first NovaSeq X Plus sequencer to the Broad Institute

14. 02. 2023 - Illumina Reports Financial Results for Fourth Quarter and Fiscal Year 2022

13. 02. 2023 - How organizations around the world are closing the cancer care gap

09. 02. 2023 - WEBINAR: Respiratory Pathogen ID and AMR Panel – A precision metagenomics solution for respiratory pathogen identification

08. 02. 2023 - Illumina Appoints Joydeep Goswami Chief Financial Officer

07. 02. 2023 - VIDEO: UK Festival of Genomics & Biodata inspires and connects industry leaders

01. 02. 2023 - WEBINAR: Multiomic profiling of patient-derived subclones identifies aggressive cellular subpopulations in paediatric diffuse high-grade gliomas

31. 01. 2023 - Sequencing within reach, for any application

26. 01. 2023 - WEBINAR: Empower murine studies to accelerate cancer research

17. 01. 2023 - Illumina to Announce Fourth Quarter and Full Year 2022 Financial Results on Tuesday, February 7, 2023

16. 01. 2023 - Meet NovaSeq X Series

16. 01. 2023 - Illumina and Nashville Biosciences Announce Sequencing Agreement with Amgen

12. 01. 2023 - Does Your Dog Have Nine Lives, Too? This DNA Test Can Tell You

10. 01. 2023 - WEBINAR: Clonal evolution in breast cancer: application of ultra-deep single cell multiomic sequencing

09. 01. 2023 - Experts in Hungary and the Czech Republic share their experiences using Comprehensive Genomic Profiling

02. 01. 2023 - Illumina Ranks Among Top Scores on Dow Jones Sustainability Index and CDP

01. 01. 2023 - Get-to-know (PDF)

22. 12. 2022 - The Next Frontier in Carbon Capture is a Hungry Bacterium

15. 12. 2022 - WEBINAR: A multi-species, low-cost, genome-wide genotyping platform to support molecular breeding in small grains

06. 12. 2022 - Addressing the Shortage of Genetic Counselors with Software

28. 11. 2022 - WEBINAR: Shining a Light on Rare Disease

22. 11. 2022 - Addressing the Shortage of Genetic Counselors with Software

21. 11. 2022 - RNA Sequencing Critical to Identifying Key Fusions for Oncology Patients

14. 11. 2022 - Greenwood Genetic Center: Answering the Unanswered

08. 11. 2022 - Can Genomics Stop the World’s Leading Cause of Death?

31. 10. 2022 - WEBINAR: Xenium In Situ - Welcome to the revolution

20. 10. 2022 - WEBINAR: Resolving tumor microenvironment heterogeneity at the single cell level from fixed samples

17. 10. 2022 - Illumina Unveils Revolutionary NovaSeq X Series to Rapidly Accelerate Genomic Discoveries and Improve Human He

10. 10. 2022 - Illumina Introduces Multiple Breakthrough Sequencing Innovations at Inaugural Genomics Forum

03. 10. 2022 - The Illumina Innovation Roadmap: Empowering Genomic Breakthroughs

26. 09. 2022 - Illumina Genomics Forum to Convene Leading Visionaries to Explore Architecting Health's Radically New Infrastr

19. 09. 2022 - Illumina Genomics Forum

12. 09. 2022 - WEBINAR: An Introduction to Sequencing

06. 09. 2022 - WEBINAR: Where do I begin with IVDR? Illumina - The basics, the transition and how we can help

31. 08. 2022 - WEBINAR: Metatranscriptomic Analysis of the Skin and Gut Microbiomes of an Isolated Amazonian Community

29. 08. 2022 - 50 Patents in 25 Years: A Look Back on the Sequence of Dr. Colin Barnes’s Career

22. 08. 2022 - Illumina Genomics Forum to Feature Bill Gates and Distinguished Health Leaders Addressing Need for Global Acce

16. 08. 2022 - Illumina Unveils its Most Accurate and Comprehensive Secondary Analysis Platform

08. 08. 2022 - The Soil Secrets That Could Help Feed the World

04. 08. 2022 - Inaugural Illumina Genomics Forum with a Conversation with Former U.S. President Barack Obama

26. 07. 2022 - Illumina Invests in £30M Venture Fund to Advance Breakthroughs in Human Health

19. 07. 2022 - Illumina Research Test Codeveloped with Merck to Unlock Deeper Insights into the Tumor Genome

12. 07. 2022 - Australia’s PrOSPeCT Project Is Sequencing Thousands of Cancer Patients

04. 07. 2022 - AI Drives Data Insights for Doctors and their Patients

27. 06. 2022 - Video: European Customers Share Their Success Stories

20. 06. 2022 - “All Patients Should Have Their Tumor Sequenced At Least Once”

15. 06. 2022 - WEBINAR: Single-cell transcriptomic landscape in Alzheimer’s disease

06. 06. 2022 - Illumina Introduces New Pan-Cancer Companion Diagnostic to Match Patients to Targeted Therapy

31. 05. 2022 - Baby Fitz’s Life-Saving Diagnosis Through Whole-Genome Sequencing

23. 05. 2022 - WEBINAR: A comprehensive solution for virtually any application: NextSeq 1000 and 2000

16. 05. 2022 - 1st 10x Genomics Experience Meeting 2022

09. 05. 2022 - WEBINAR: Introducing Illumina Infinity long read technology

02. 05. 2022 - WEBINAR: Advancements in translational biomarker identification from cell-free RNA

25. 04. 2022 - WEBINAR: Can genomic surveillance detect the next pandemic before it’s too late?

14. 04. 2022 - For Kidney Transplant Recipients, a More Accurate and Tailored Care Plan

07. 04. 2022 - Can Wastewater Surveillance Protect Public Health?

30. 03. 2022 - WEBINAR: Enabling in-house comprehensive genomic profiling for today's and tomorrow's clinical needs

28. 03. 2022 - WEBINAR: Illumina VIP Event

21. 03. 2022 - WEBINAR: Spatiotemporal analysis of cardiac tissue during myocardial infarction

14. 03. 2022 - Scaling to the cloud to support whole-genome sequencing

08. 03. 2022 - Skis, Skincare, and More: Making Better Products with Algae

21. 02. 2022 - From Patents to Patients: Meet the Women Making a Difference at Illumina

14. 02. 2022 - Patient Success Story: Beating Stage IV Lung Cancer

07. 02. 2022 - Illumina and Boehringer Ingelheim Announce Companion Diagnostic Partnership

01. 02. 2022 - Let it Grow: A DNA Database for Plants, One Species at a Time

26. 01. 2022 - 2021 in Genomics

18. 01. 2022 - Laboratóriumi folyadékkezelő automatizálási megoldások

18. 11. 2020 - WEBINAR for ALL: Single cell sequencing and spatial transcriptomics - Nov. 23-rd, 14:00

04. 11. 2020 - Az Illumina 2020 őszi virtuális eseményei !

27. 10. 2020 - ASHG’s Annual Meeting Goes Virtual

22. 10. 2020 - Delivering high-confidence DNA variant, RNA fusion and TMB data

15. 10. 2020 - Exploring Immunity—Linking Highly Multiplexed Antigen Recognition to Immune Repertoire and Phenotype

25. 09. 2020 - Using Single-Cell Multiomics to Reveal New Insights into Uveal Melanoma Evolution

22. 09. 2020 - Oncology variant interpretation just got more precise

23. 01. 2017 - Illumina - Egy új korszak kezdete a szekvenálásban!

DNA_D_(002)4.png

logo_seqone_(003)2.png

Quantum_SI_no_background_(002)2.png