Fulgent Genetics, Inc. · NASDAQ:FLGT

Fulgent Genetics — Q2 2022 Earnings Presentation

28 slides from Fulgent Genetics's earnings presentation, Aug 4, 2022

  1. Slide 1: Exhibit 99.2

    Exhibit 99.2

  2. Slide 2: Forward-Looking Statements and Market Data

    Disclaimer Forward-Looking Statements and Market Data This presentation contains forward-looking statements, which are statements other than those of historical facts and which represent the estimates and expectations of Fulgent Genetics, Inc. (the “Company”) about future events based on current vie

  3. Slide 3: Mission, Core Values, and Strategy

    Mission, Core Values, and Strategy Mission Develop flexible and affordable genomic testing that improves the everyday lives of those around us Core Values Innovation Customer service and commitment Quality Efficiency Strategy Leverage our proprietary NGS platform for broad application Operational ex

  4. Slide 4: Leadership Team

    Leadership Team Esteemed background in molecular science and pathology Most recently Chief Medical Officer at NeoGenomics; prior senior role at Clarient. Chairman Emeritus of Pathology at City of Hope National Medical Center Brandon Perthuis Chief Commercial Officer Dr. Lawrence Weiss Chief Medical

  5. Slide 5: History of Fulgent Genetics

    Dr. Larry Weiss Ming Hsieh Paul Kim James Xie Dr. Harry Gao History of Fulgent Genetics Vision of being one-stop shop for genomic testing Integrating acquisitions and partnerships Capital deployment in M&A opportunities Disciplined execution with expanding team 2011 2022 & Beyond 2020 2021 2015-2019

  6. Slide 6: Fulgent is Positioned to Execute on Our Growth Strategy

    Well positioned to execute on a growth strategy that includes organic and inorganic initiatives, including: Transformational acquisition of Inform Diagnostics Ramping and integration of capabilities of CSI Labs Scaling partnerships – Helio Health and Spatial Genomics Potential future acquisitions wi

  7. Slide 7: Inform Diagnostics Acquisition

    Inform Diagnostics Acquisition Inform Diagnostics Strategic Highlights Test Menu Expansion: Acquisition extends Fulgent’s capabilities into the pathology testing market Commercial Synergies: With the addition of Inform Diagnostics’ extensive testing capabilities, nationwide salesforce, and significa

  8. Slide 8: CSI Laboratories Acquisition

    CSI Laboratories Acquisition CSI Laboratories Strategic Highlights Enter High Value Markets: Expansion into somatic genetic testing market, which is expected to grow to $16.8 billion by 2030 Revenue Synergy Opportunities: Leveraging Fulgent’s best-in-class technology and Next Generation Sequencing (

  9. Slide 9: Target Market Opportunity

    Target Market Opportunity Cancer Diagnostics $80B market1 Market sizes sourced from Wall Street equity research Market size sourced from Frost & Sullivan Genes & Panels Tumor Profiling Known Mutation Newborn Genetics Hereditary Cancer Carrier Screens Genomic Testing Sequencing Service Infectious Dis

  10. Slide 10: Building Fulgent's Platform and Capabilities

    Building Fulgent’s Platform and Capabilities Cancer Diagnostics Reproductive Health Early Detection / Liquid Biopsy Genes & Panels Tumor Profiling Known Mutation Newborn Genetics Hereditary Cancer Carrier Screens Genomic Testing Sequencing Service seqFISH Technology Comprehensive Diagnostics Platfor

  11. Slide 11: What Sets Fulgent Apart?

    What Sets Fulgent Apart? Represents genes covered by single-gene tests. For Q2 2022. Includes all tests available for sale (e.g., Whole Exome, Whole Genome, Large Panels, Small Panels, Comprehensive and Focus Cancer Panels and Single-Gene Tests, COVID-19 Tests, and vaccines). Also excludes stock-bas

  12. Slide 12: Proprietary Technology Platform

    Proprietary Technology Platform Differentiated Technology... Engineered genetic biochemistry, including reagents and probes Data suppression and comparison algorithms Adaptive learning software Automated reporting …Provides a Multitude of Advantages Broadest test menu Ability to rapidly develop and

  13. Slide 13: Commercialized Offerings and Recent Traction

    Commercialized Commercialized COVID-19 Testing Specialized Oncology Testing Core NGS Recent Traction with: Hereditary Cancer Cardiovascular Genetics Reproductive Health Neurodegenerative Genetics Newly launched pharmacogenetic test Aggressively expanding sales and commercial organization Wide Array

  14. Slide 14: Fulgent's Menu is Scalable and Affordable to Customers

    For Q2 2022. Includes all tests available for sale (e.g., Whole Exome, Whole Genome, Large Panels, Small Panels, Comprehensive and Focus Cancer Panels and Single-Gene Tests, COVID-19 Tests, and vaccines). Also excludes stock-based compensation. See GAAP reconciliation. Fulgent’s Menu is Scalable and

  15. Slide 15: NGS Testing – Offerings

    NGS Testing – Offerings Site-Specific Testing Known Mutation Focus (30 Genes) Comprehensive (127 Genes) Somatic Cancer Panels 19 Panels Repeat Expansion 18,400+ Genes Single Gene 900+ Panels Customizable Panels Disease Panels Clinical Exome (4,500+ Genes) Whole Exome Exome Tests

  16. Slide 16: NGS Testing – Germline Oncology Test Menu

    NGS Testing – Germline Oncology Test Menu Fulgent Focus Cancer Panels Fulgent Comprehensive Cancer Panels Customizable: Add additional cancer genes or panels at no charge Genes: 30 Methods: NGS & Del/Dup Coverage: 99% at 50x Del/Dup ≥ 1 Exon TAT: 2 – 3 Weeks Customizable: Add additional cancer genes

  17. Slide 17: FISH Oncology Testing Platforms

    FISH Oncology Testing Platforms Expansive heme and solid tumor menu STAT testing available PML/RARA <1 day TAT CD138 cell enrichment for PCM 3-5 Day turnaround time 225+ stains Platform agnostic Roche, Agilent and Leica IHC Three levels of service – Tech, Global, Consultative PD-L1 - Various IVD pla

  18. Slide 18: NGS Testing – Panel Deep Dive

    The Focus Carrier screen is a pan-ethnic screen that looks for pathogenic mutations known to cause autosomal recessive and X-linked disorders Gene Count: 30 The Ashkenazi Jewish carrier screens for pathogenic carrier variants known to cause recessive genetic disorders Gene Count: 61 The ACOG/ACMG pa

  19. Slide 19: NGS Testing – Women's Health: PGT-A

    NGS Testing – Women’s Health: PGT-A Increased Chance of Pregnancy Embryos with a normal number of chromosomes have a better chance of resulting in successful pregnancy More Confidence in Transferring a Single Embryo Avoid health risks associated with twin or triplet pregnancies that can occur from m

  20. Slide 20: NGS Testing – Rapid Whole Genome for Newborns

    NGS Testing – Rapid Whole Genome for Newborns Screens for over 200 health conditions Identifies potential health risks before symptoms arise Early detection known to have a positive impact Simple cheek swab collection for your baby : No pricks, sticks, or tears necessary Newborn Genetic Screening Go

  21. Slide 21: Consumer Initiated Tests – Picture Genetics

    Parenting Carrier test that screens for genes associated with 30 genetic conditions Newborn Screens newborns for genes associated with various genetic conditions Wellness Screens adults for genetic variants that indicate disease risk PD Aware Assesses risk for Parkinson's Disease COVID-19 Infection

  22. Slide 22: Summary Financial Performance

    Summary Financial Performance $45M Core Revenue1 as of Q2’22 $429M LTM Operating Cash Flow as of Q2’22 ~339,000 LTM Core Tests as of Q2’22 102% growth year-over-year ~160% growth year-over-year ($ in thousands) +107% year-over-year Core Revenue excludes NGS COVID-19 test volume

  23. Slide 23: Financial Performance: Revenue Profile

    Financial Performance: Revenue Profile ($ in thousands) (in thousands) ($ in thousands) (in thousands) Core Revenue excludes NGS COVID-19 test volume

  24. Slide 24: Financial Performance: Margin Profile

    Figure is not in accordance with GAAP because it does not include equity-based compensation, amortization, restructuring cost, and acquisition-related costs. (1) Financial Performance: Margin Profile (1) (in thousands) (1)

  25. Slide 25: 2022 Financial Guidance

    2022 Financial Guidance Q3 2022 Full Year 2022 Change from Prior Quarter RT-PCR COVID-19 $51 M $480 M Unchanged NGS COVID-19 (CDC) Fulgent Core NGS $54 M + 101% y/y1 $185 M + 99% y/y1 + $5 M CSI and Inform Diagnostics Contributions Total $105 M -54% y/y $665 M -33% y/y + $5 M COVID Core Core Revenue

  26. Slide 26: Balance Sheet

    Balance Sheet jin 0008) Cash & cash equivalents Marketable securities Trade accounts receivable, net tne current assets Total current assets Marketable securities, long-term Redeemable prefered stock investment Fired assets, net Intangible assets, net Goodwill ther long-term assets Total assets Peri

  27. Slide 27: Non-GAAP Financial Adjustments

    Non-GAAP Financial Adjustments

  28. Slide 28: Founded in 2011 | Located in Los Angeles, CA

    Founded in 2011 | Located in Los Angeles, CA | NASDAQ:FLGT

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