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Edico Genome

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uuid0003h98

Namestring
Edico Genome
Legal namestring
Edico Genome
Websiteurl
edicogenome.com
Company typeenum
Private
Founded yearint
2013
Descriptiontext

Edico Genome, founded in 2013 in San Diego, developed the DRAGEN (Dynamic Read Analysis for GENomics) bioinformatics platform for secondary analysis of next-generation sequencing (NGS) data. The platform replaces up to 30 open-source tools with a single validated pipeline supporting germline, somatic, RNA, and methylation analysis, and is differentiated by hardware-accelerated processing (FPGA), pangenome-based multi-genome mapping, and lossless ORA compression. Edico Genome was acquired by Illumina and now operates as a wholly-owned subsidiary; DRAGEN is distributed through Illumina's global enterprise sales organization with deployment options including on-premises servers, cloud, and onboard integration with Illumina sequencers (NovaSeq X, NextSeq 1000/2000, MiSeq i100).

The company serves a horizontal customer base spanning life science researchers, clinical laboratories, pharmaceutical and biotech firms, and oncology research programs, with named enterprise references including UK Biobank, Cardio-CARE, and Basepaws. DRAGEN's value proposition is anchored in independently verified accuracy (99.90% on the PrecisionFDA Truth Challenge v2), world-record processing speeds (~34 minutes for a 40x genome), and material storage cost reductions (80% via built-in lossless compression). Recent product releases (v4.3 in 2024, v4.4 in 2025) have expanded DRAGEN into clinical oncology (Heme WGS, Solid WGS tumor-normal, Minimal Residual Disease), population-scale variant aggregation (Iterative gVCF Genotyper), and pharmacogenomics (PGx pipeline).

Pricing is not publicly disclosed; the primary call-to-action is 'Request a demo,' indicating a consultative enterprise sales motion. Pre-acquisition, the company raised approximately $32 million across seed (2013, EvoNexus), Series A (2014, $10M led by Qualcomm Ventures), and Series B (2017, $22M led by Dell Technologies Capital). Since the Illumina acquisition, Edico Genome has not operated as an independent commercial entity, and DRAGEN-specific revenue is not separately disclosed in Illumina's reporting.

Short descriptiontext

Edico Genome, now an Illumina subsidiary, develops the DRAGEN bioinformatics platform for NGS secondary analysis, serving research, clinical, pharma, and oncology customers with hardware-accelerated variant calling, population-scale pipelines, and onboard integration with Illumina sequencers.

Operating statusenum
Acquired
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersSan Diego, United States
HQ citystring
San Diego
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Keyword5 values
NGS data analysis, bioinformatics software, genomic sequencing, variant calling, secondary analysis
Industry2 codes
1Bioinformatics & Multi-omics Analysis Software
CodeHLAGAJADPrimaryYes
2Genomics & Next-Generation Sequencing (NGS) Services
CodeHLAGANAAPrimaryNo
NAICS code1 code
  • Software Publishers5132
SIC code1 code
  • Services-Prepackaged Software7372
Product category
Bioinformatics Software
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels4 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Technology or R&D, Personnel, Marketing or Sales, Infrastructure, Operations
GTM typeB2B
B2B
Offering typeSoftware
Software
Brand1 record
1DRAGEN Bio-IT Platform
Description

Former name of the bioinformatics pipeline product developed by Edico Genome for secondary analysis of NGS data. Renamed to DRAGEN secondary analysis after acquisition by Illumina.

illumina.com
Core offering1 text field

Edico Genome developed DRAGEN (Dynamic Read Analysis for GENomics), a hardware-accelerated bioinformatics platform that performs secondary analysis of next-generation sequencing (NGS) data. The platform replaces up to 30 open-source tools with a single solution supporting whole-genome, exome, methylome, and transcriptome analysis, deployable on-premises, in the cloud, or directly onboard Illumina sequencers.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 6 values shown
  • 99.90% accuracy score on Precision FDA Truth Challenge v2 benchmark data
+5 more records
Product overview1 text field

Edico Genome, now part of Illumina, developed DRAGEN (Dynamic Read Analysis for GENomics) secondary analysis software — a comprehensive bioinformatics platform for NGS data processing. The core product is DRAGEN Secondary Analysis (formerly DRAGEN Bio-IT Platform), which consolidates up to 30 open-source tools into a single solution. The platform includes specialized pipelines for Germline (whole-genome and enrichment), Somatic (whole-genome, enrichment, tumor-only, and tumor-normal), RNA, and Methylation analysis. Additional modules include the Iterative gVCF Genotyper (IGG) for population-scale variant discovery, the PGx pipeline for pharmacogenomics, and ORA compression for efficient data storage. The software is deployable via on-premises server, cloud-based, or directly onboard Illumina sequencers including NovaSeq X Series, NextSeq 1000/2000, and MiSeq i100 Series.

Product and service7 records
1DRAGEN Secondary Analysis
CategoryBioinformatics Software
Description

A comprehensive bioinformatics software suite for processing next-generation sequencing data, providing accurate and efficient secondary analysis including variant calling, alignment, and genomic data processing for whole genomes, exomes, methylomes, and transcriptomes. Targeted at genomic researchers, clinical laboratories, and pharmaceutical companies.

2DRAGEN Germline Pipeline
CategoryBioinformatics Software
Description

Germline variant calling pipeline supporting both whole-genome and enrichment (targeted) analysis workflows for identifying inherited genetic variants in research and clinical genomics.

3DRAGEN Somatic Pipeline
CategoryBioinformatics Software
Description

Somatic variant calling pipeline supporting whole-genome and enrichment analysis with tumor-only and tumor-normal comparison workflows for oncology research and precision medicine applications.

4DRAGEN RNA Pipeline
CategoryBioinformatics Software
Description

Transcriptome analysis pipeline for RNA sequencing data processing and differential expression analysis, used in gene expression research studies.

5DRAGEN Methylation Pipeline
CategoryBioinformatics Software
Description

Epigenomic analysis pipeline for processing methylome data from bisulfite sequencing experiments, enabling epigenetic studies.

6DRAGEN Iterative gVCF Genotyper (IGG)
CategoryBioinformatics Software
Description

Population-scale variant discovery solution enabling fast aggregation and genotyping of small germline variants across large cohorts, with incremental analysis so new sample batches can be added without reprocessing the entire dataset. Used for biobank-scale and population genomics research.

7DRAGEN PGx Pipeline
CategoryBioinformatics Software
Description

Pharmacogenomics pipeline enabling genotyping of 20 genes related to drug metabolism to support drug development research and pharmacogenomic studies.

Partnership1 partner
Strategic tierCoreTypeOEM/ Whitelabel/ Licensing Partner
Description

Edico Genome developed DRAGEN technology which was acquired by Illumina. Illumina now owns, markets, and distributes the DRAGEN secondary analysis platform as part of its bioinformatics portfolio. The technology is available through Illumina's sales channels, integrated onboard Illumina sequencers, and delivered via Illumina's cloud and on-premises deployment options.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers8 records
TypeDirect peer
Description

DNAnexus provides a cloud genomics platform hosting pipelines and tertiary analysis for clinical and translational customers. It directly competes with cloud-deployed DRAGEN and is used by similar pharma, clinical, and large-scale consortia (NIH, Genomics England-adjacent projects).

TypeEmerging player
Description

Fabric Genomics (acquired by Illumina) provides AI-powered clinical genome interpretation. It sits downstream of DRAGEN and represents an emerging interpretive layer rather than a direct pipeline competitor, but competes for the same clinical genomics customer wallet.

TypeDirect peer
Description

Partek Flow and Partek EpiCenter provide NGS and multi-omics analysis software used by the same life-science researcher and translational genomics customers as DRAGEN. Recently acquired by Illumina, it sits alongside DRAGEN in Illumina's informatics portfolio — most analogous in target market and product category.

TypeEmerging player
Description

SOPHiA DDM is an AI-driven multimodal genomics analysis platform targeting clinical diagnostics, particularly oncology and rare disease. It overlaps with DRAGEN at the secondary/tertiary analysis boundary but focuses on hospital lab deployment with CE-IVD/FDA pathways — a different distribution and clinical thesis.

TypeBroad incumbent
Description

QIAGEN's CLC Genomics Workbench and QIAseq/HSP-derived pipeline ecosystem serve the same primary bioinformatics customers with a broader wet-lab + dry-lab portfolio. It is a broader incumbent — overlapping in NGS analysis but extending into instruments, reagents, and interpretation that DRAGEN does not cover.

TypeDirect peer
Description

Velsera operates a cloud-based genomics analysis platform (Seven Bridges Platform, Cancer Genomics Cloud) supporting secondary and tertiary analysis workflows. It competes directly with DRAGEN for population-scale and clinical genomics deployments, particularly via cloud distribution rather than on-prem hardware.

TypeDirect peer
Description

Sentieon provides production-grade NGS secondary analysis pipelines (DNAscope, TNseq, Haplotyper) focused on clinical-grade accuracy and speed. It is the most direct head-to-head competitor to DRAGEN for germline/somatic variant calling and shares the same customer base of clinical labs and sequencing centers.

TypeDirect peer
Description

Golden Helix (VarSeq + SVS) offers secondary and tertiary NGS analysis with a focus on annotating and filtering variants for clinical reporting. It overlaps with DRAGEN downstream — used by similar clinical labs, often layering on top of pipeline outputs to make medical-grade variant calls.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers3 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment4 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile5 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI capability2 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature9 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles1 record

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds3 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors7 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Edico Genome

Bioinformatics Softwareedicogenome.com

Edico Genome, now an Illumina subsidiary, develops the DRAGEN bioinformatics platform for NGS secondary analysis, serving research, clinical, pharma, and oncology customers with hardware-accelerated variant calling, population-scale pipelines, and onboard integration with Illumina sequencers.

What Edico Genome does

Edico Genome, founded in 2013 in San Diego, developed the DRAGEN (Dynamic Read Analysis for GENomics) bioinformatics platform for secondary analysis of next-generation sequencing (NGS) data. The platform replaces up to 30 open-source tools with a single validated pipeline supporting germline, somatic, RNA, and methylation analysis, and is differentiated by hardware-accelerated processing (FPGA), pangenome-based multi-genome mapping, and lossless ORA compression. Edico Genome was acquired by Illumina and now operates as a wholly-owned subsidiary; DRAGEN is distributed through Illumina's global enterprise sales organization with deployment options including on-premises servers, cloud, and onboard integration with Illumina sequencers (NovaSeq X, NextSeq 1000/2000, MiSeq i100).

The company serves a horizontal customer base spanning life science researchers, clinical laboratories, pharmaceutical and biotech firms, and oncology research programs, with named enterprise references including UK Biobank, Cardio-CARE, and Basepaws. DRAGEN's value proposition is anchored in independently verified accuracy (99.90% on the PrecisionFDA Truth Challenge v2), world-record processing speeds (~34 minutes for a 40x genome), and material storage cost reductions (80% via built-in lossless compression). Recent product releases (v4.3 in 2024, v4.4 in 2025) have expanded DRAGEN into clinical oncology (Heme WGS, Solid WGS tumor-normal, Minimal Residual Disease), population-scale variant aggregation (Iterative gVCF Genotyper), and pharmacogenomics (PGx pipeline).

Pricing is not publicly disclosed; the primary call-to-action is 'Request a demo,' indicating a consultative enterprise sales motion. Pre-acquisition, the company raised approximately $32 million across seed (2013, EvoNexus), Series A (2014, $10M led by Qualcomm Ventures), and Series B (2017, $22M led by Dell Technologies Capital). Since the Illumina acquisition, Edico Genome has not operated as an independent commercial entity, and DRAGEN-specific revenue is not separately disclosed in Illumina's reporting.

Edico Genome firmographics

Firmographics
Name
Edico Genome
Legal name
Edico Genome
Website
https://edicogenome.com
Company type
Private
Founded year
2013
Operating status
Acquired
Headcount range
11–50 employees
Short description
Edico Genome, now an Illumina subsidiary, develops the DRAGEN bioinformatics platform for NGS secondary analysis, serving research, clinical, pharma, and oncology customers with hardware-accelerated variant calling, population-scale pipelines, and onboard integration with Illumina sequencers.
Ownership category
akta.pro rank

Edico Genome industry classification

Industry
Product category
Bioinformatics Software
NAICS
Software Publishers (5132)
SIC
Services-Prepackaged Software (7372)
akta.pro primary industry
Bioinformatics & Multi-omics Analysis Software (HLAGAJAD)
akta.pro secondary industry
Genomics & Next-Generation Sequencing (NGS) Services (HLAGANAA)

Keywords

  • NGS data analysis
  • Bioinformatics software
  • Genomic sequencing
  • Variant calling
  • Secondary analysis

Where Edico Genome is headquartered

Location

Headquarters

HQ city
San Diego
HQ country
United States
HQ region
North America

Markets served

Edico Genome business model

Business model
GTM type
B2B
Offering type
Software
Cost components
Technology or R&D, Personnel, Marketing or Sales, Infrastructure, Operations

Distribution channels4 records

Marketing channels5 records

Edico Genome product offering

Product offering

Core offering

Edico Genome developed DRAGEN (Dynamic Read Analysis for GENomics), a hardware-accelerated bioinformatics platform that performs secondary analysis of next-generation sequencing (NGS) data. The platform replaces up to 30 open-source tools with a single solution supporting whole-genome, exome, methylome, and transcriptome analysis, deployable on-premises, in the cloud, or directly onboard Illumina sequencers.

Product overview

Edico Genome, now part of Illumina, developed DRAGEN (Dynamic Read Analysis for GENomics) secondary analysis software — a comprehensive bioinformatics platform for NGS data processing. The core product is DRAGEN Secondary Analysis (formerly DRAGEN Bio-IT Platform), which consolidates up to 30 open-source tools into a single solution. The platform includes specialized pipelines for Germline (whole-genome and enrichment), Somatic (whole-genome, enrichment, tumor-only, and tumor-normal), RNA, and Methylation analysis. Additional modules include the Iterative gVCF Genotyper (IGG) for population-scale variant discovery, the PGx pipeline for pharmacogenomics, and ORA compression for efficient data storage. The software is deployable via on-premises server, cloud-based, or directly onboard Illumina sequencers including NovaSeq X Series, NextSeq 1000/2000, and MiSeq i100 Series.

Differentiator

Problem solved

Functional benefit

Brands

  • DRAGEN Bio-IT Platform: Former name of the bioinformatics pipeline product developed by Edico Genome for secondary analysis of NGS data. Renamed to DRAGEN secondary analysis after acquisition by Illumina.

Products and services

  • DRAGEN Secondary Analysis A comprehensive bioinformatics software suite for processing next-generation sequencing data, providing accurate and efficient secondary analysis including variant calling, alignment, and genomic data processing for whole genomes, exomes, methylomes, and transcriptomes. Targeted at genomic researchers, clinical laboratories, and pharmaceutical companies.
  • DRAGEN Germline Pipeline Germline variant calling pipeline supporting both whole-genome and enrichment (targeted) analysis workflows for identifying inherited genetic variants in research and clinical genomics.
  • DRAGEN Somatic Pipeline Somatic variant calling pipeline supporting whole-genome and enrichment analysis with tumor-only and tumor-normal comparison workflows for oncology research and precision medicine applications.
  • DRAGEN RNA Pipeline Transcriptome analysis pipeline for RNA sequencing data processing and differential expression analysis, used in gene expression research studies.
  • DRAGEN Methylation Pipeline Epigenomic analysis pipeline for processing methylome data from bisulfite sequencing experiments, enabling epigenetic studies.
  • DRAGEN Iterative gVCF Genotyper (IGG) Population-scale variant discovery solution enabling fast aggregation and genotyping of small germline variants across large cohorts, with incremental analysis so new sample batches can be added without reprocessing the entire dataset. Used for biobank-scale and population genomics research.
  • DRAGEN PGx Pipeline Pharmacogenomics pipeline enabling genotyping of 20 genes related to drug metabolism to support drug development research and pharmacogenomic studies.

Quantifiable outcome

  • 99.90% accuracy score on Precision FDA Truth Challenge v2 benchmark data
  • +5 more outcomes

Companies that use Edico Genome

Customer profile

Named customers3 records

Segments4 records

Ideal customer profiles5 records

Edico Genome technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

AI capability2 records

Feature9 records

Edico Genome partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • IlluminacoreOEM/ Whitelabel/ Licensing PartnerEdico Genome developed DRAGEN technology which was acquired by Illumina. Illumina now owns, markets, and distributes the DRAGEN secondary analysis platform as part of its bioinformatics portfolio. The technology is available through Illumina's sales channels, integrated onboard Illumina sequencers, and delivered via Illumina's cloud and on-premises deployment options.

Recent moves6 records

Expansion highlights5 records

Edico Genome competitors and assessment

Company assessment

Direct peers

  • DNAnexus: DNAnexus provides a cloud genomics platform hosting pipelines and tertiary analysis for clinical and translational customers. It directly competes with cloud-deployed DRAGEN and is used by similar pharma, clinical, and large-scale consortia (NIH, Genomics England-adjacent projects).
  • Partek (now part of Illumina): Partek Flow and Partek EpiCenter provide NGS and multi-omics analysis software used by the same life-science researcher and translational genomics customers as DRAGEN. Recently acquired by Illumina, it sits alongside DRAGEN in Illumina's informatics portfolio — most analogous in target market and product category.
  • Velsera (formerly Seven Bridges Genomics): Velsera operates a cloud-based genomics analysis platform (Seven Bridges Platform, Cancer Genomics Cloud) supporting secondary and tertiary analysis workflows. It competes directly with DRAGEN for population-scale and clinical genomics deployments, particularly via cloud distribution rather than on-prem hardware.
  • Sentieon: Sentieon provides production-grade NGS secondary analysis pipelines (DNAscope, TNseq, Haplotyper) focused on clinical-grade accuracy and speed. It is the most direct head-to-head competitor to DRAGEN for germline/somatic variant calling and shares the same customer base of clinical labs and sequencing centers.
  • Golden Helix: Golden Helix (VarSeq + SVS) offers secondary and tertiary NGS analysis with a focus on annotating and filtering variants for clinical reporting. It overlaps with DRAGEN downstream — used by similar clinical labs, often layering on top of pipeline outputs to make medical-grade variant calls.

Emerging players

  • Fabric Genomics: Fabric Genomics (acquired by Illumina) provides AI-powered clinical genome interpretation. It sits downstream of DRAGEN and represents an emerging interpretive layer rather than a direct pipeline competitor, but competes for the same clinical genomics customer wallet.
  • SOPHiA GENETICS: SOPHiA DDM is an AI-driven multimodal genomics analysis platform targeting clinical diagnostics, particularly oncology and rare disease. It overlaps with DRAGEN at the secondary/tertiary analysis boundary but focuses on hospital lab deployment with CE-IVD/FDA pathways — a different distribution and clinical thesis.

Broad incumbents

  • QIAGEN Digital Insights (CLC bio, QIAseq): QIAGEN's CLC Genomics Workbench and QIAseq/HSP-derived pipeline ecosystem serve the same primary bioinformatics customers with a broader wet-lab + dry-lab portfolio. It is a broader incumbent — overlapping in NGS analysis but extending into instruments, reagents, and interpretation that DRAGEN does not cover.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights7 records

Customer concentration

Edico Genome social profiles

Digital presence

Edico Genome financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Edico Genome leadership team

Management profile

Number of profiles

Profiles1 record

Edico Genome funding detail

Funding detail

Funding overview

Funding rounds3 records

Investors7 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Edico Genome M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Edico Genome

What does Edico Genome do?

Edico Genome developed DRAGEN (Dynamic Read Analysis for GENomics), a hardware-accelerated bioinformatics platform that performs secondary analysis of next-generation sequencing (NGS) data. The platform replaces up to 30 open-source tools with a single solution supporting whole-genome, exome, methylome, and transcriptome analysis, deployable on-premises, in the cloud, or directly onboard Illumina sequencers.

Is Edico Genome a public or private company?

Edico Genome is a private company. It is classified as corporate owned and is currently acquired.

When was Edico Genome founded?

Edico Genome was founded in 2013. It employs 11 to 50 people.

Where is Edico Genome based?

Edico Genome is headquartered in San Diego, United States, in the North America region.

Who are Edico Genome's main competitors?

Direct peers on record are DNAnexus, Partek (now part of Illumina), Velsera (formerly Seven Bridges Genomics), Sentieon and Golden Helix. Emerging players are Fabric Genomics and SOPHiA GENETICS. QIAGEN Digital Insights (CLC bio, QIAseq) is listed as a broad incumbent.

Does Edico Genome have an API?

No public API is recorded for Edico Genome.

What industry is Edico Genome in?

Edico Genome's product category is Bioinformatics Software. Its primary akta.pro industry code is HLAGAJAD, Bioinformatics & Multi-omics Analysis Software, with a secondary code of HLAGANAA, Genomics & Next-Generation Sequencing (NGS) Services. Its NAICS code is 5132 and its SIC code is 7372.

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Live signals
PR NewswireGlobal Biotechnology Services Market Report 2021: Focus on Pharmaceutical, Biotechnological, Academic, Clinical Trial, Healthcare SectorsResearchAndMarkets published a global biotechnology services market report showing the market is expected to grow from $150.37 billion in 2020 to $163.92 billion in 2021, and reach $265.1 billion in 2025 at a compound annual growth rate of 12.8%. The report identifies collaborations and partnerships as a growing trend, highlighting Interpace Pharma's December 2019 partnership with Genecast Biotechnology for clinical trial solutions and Illumina's 2018 acquisition of Edico Genome to reduce sequencing data acquisition costs. The report also notes that risks related to genetic data and genetically modified organisms, including the mandatory bioengineered food labeling implemented in the USA from January 2020, may constrain market growth.Clinical Lab ProductsIllumina Acquires Edico Genome to Accelerate Genomic Data AnalysisIllumina Inc. of San Diego has acquired Edico Genome, also based in San Diego, a provider of next-generation sequencing data analysis acceleration solutions. Edico's Dragen bioinformatics platform uses FPGA technology and proprietary algorithms to reduce data footprint and time to results, and is currently research use only. Illumina plans to integrate the platform into its sample-to-answer workflow.InsideprecisionmedicineIllumina Acquires Edico GenomeIllumina acquired Edico Genome to expand its data analysis solutions for next-generation sequencing (NGS). The acquisition aims to accelerate data analysis and streamline workflows, leveraging Edico’s DRAGEN platform, and will integrate with Illumina’s sequencing portfolio and cloud services.PR NewswireEdico Genome Bolsters Sales And Business Development LeadershipEdico Genome, a leading secondary analysis solution provider for next-generation sequencing, announced the appointment of Mike Harkins as vice president of sales and Katherine Atkinson as vice president of business development to support its global expansion. Harkins joins from Thermo Fisher Scientific where he served as vice president of global sales overseeing bioproduction, while Atkinson comes from Illumina where she directed Global Channel Partners spanning over 70 partners across more than 130 countries. The new executives will be based at Edico Genome's San Diego headquarters and will drive growth of the company's DRAGEN Bio-IT platform.PR NewswireGenomics England Adopts Edico Genome's DRAGEN Bio-IT Platform To Increase Accuracy, Consistency Of Next-Generation Sequencing AnalysisEdico Genome and Genomics England announced a partnership at the J.P. Morgan Healthcare Conference in which Genomics England will use Edico Genome's DRAGEN Bio-IT platform to re-process 5,000 whole human genomes from individuals with rare diseases, originally mapped on the older GRCh37 reference genome, to the updated GRCh38 reference for improved accuracy and consistency. The partnership supports Genomics England's goal of making next-generation sequencing the standard of care across the U.K.'s National Health Service in 2018. Edico Genome has also joined Genomics England's Discovery Forum, which provides re-processed datasets to pharma and industry partners for additional analysis.PR NewswireEdico Genome's DRAGEN Solution For Secondary Analysis Of Genomic Data Now Available Via Seven BridgesEdico Genome and Seven Bridges announced the availability of Edico's DRAGEN genomic analysis pipelines on Seven Bridges' cloud-based platform. The integration, powered by Amazon Web Services' EC2 F1 instances, allows researchers to analyze whole human genomes in approximately 25 minutes compared to traditional methods taking 20 to 30 hours. A free trial for ten genomes is available from December 5 through January 31.Scientific ComputingA silver lining for HPC in the cloudCloud-based High-Performance Computing (HPC) is gaining traction across diverse industries such as AI, media, and healthcare, driven by providers like vScaler offering flexible infrastructure for prototyping and burst workloads. In a specific application of this trend, DNAnexus and Edico Genome partnered with Amazon Web Services to integrate their technologies, enabling rapid genome sequencing for precision medicine research. This integration has been adopted by the Rady Children’s Institute for Genomic Medicine to facilitate rapid diagnosis and targeted treatment for critically ill patients.PR NewswireChildren's Hospital of Philadelphia And Edico Genome Achieve Fastest-Ever Analysis Of 1,000 GenomesChildren's Hospital of Philadelphia and Edico Genome set a Guinness World Record by analyzing 1,000 pediatric whole genomes in two hours and twenty-five minutes, demonstrating a new standard for rapid genome processing. The analysis was conducted using Edico Genome's DRAGEN Genome Pipeline deployed on 1,000 Amazon EC2 F1 instances on the AWS Cloud, drawing on FPGA-enabled computing power to process samples from CHOP's Center for Applied Genomics. Results will be used to investigate genetic links to common childhood diseases including asthma, autism, diabetes and pediatric cancer, advancing the goal of bringing precision medicine into mainstream clinical practice.PR NewswireEdico Genome And Fabric Genomics Develop Integrated Solution For Genomic Analysis With The Goal Of Improving Clinical CareEdico Genome and Fabric Genomics announced a partnership at the American Society for Human Genetics Annual Meeting to integrate Edico's DRAGEN Bio-IT platform with Fabric's Opal Clinical variant interpretation platform for secondary and tertiary analysis of next-generation sequencing data. The combined solution, already deployed successfully at Rady Children's Institute for Genomic Medicine for one year, can analyze a whole human genome in approximately 20 minutes with high accuracy, aiming to improve clinical care for inherited diseases and oncology. The partnership leverages machine learning algorithms to identify disease-causing variants and is positioned to advance personalized medicine adoption.PR NewswireEdico Genome And South Africa's Centre For Proteomic And Genomic Research Deploy First DRAGEN Bio-IT Platform In AfricaEdico Genome and the Centre for Proteomic and Genomic Research (CPGR) announced the deployment of the first DRAGEN Bio-IT platform in Africa at CPGR's facility in Cape Town. This hardware-accelerated solution is designed to significantly reduce genomic data analysis times, supporting South Africa's life science community in advancing precision medicine. The deployment marks a strategic expansion of Edico Genome's technology into the African market.