- Genomics and Gene Editing 2026
- Chapter 3
Systems and sectors at baseline
Contents
- ·Edition home
- ·Executive summary
- 1Genomics is data infrastructure and a therapeutic frontier
- 2Key findings
- 3Systems and sectors at baseline
- 4Risks and capability
- 5Individualised editing outpaces delivery systems
- 6Readings from the other desks
- 7The 2027 agenda
- 8Systems in depth
- AMethodology
- BData appendix
- CReferences and record
- ·Complete edition, for print
3.1Where each system stood at evidence close
HLT · Therapy
Evaluable sickle cell patients free of severe crises
97%29 of 30 patients, 12 months or more.
Reported2024NEJM2
DAT · Reference
Base pairs in the complete T2T-CHM13 sequence
3.055billionnearly 200 million base pairs new.
Reported2022Science11
DAT · Biobanks
Participants with whole genomes in UK Biobank
490,640participantsreleased in 2025.
Reported2025Nature16
FIN · Finance
Casgevy revenue in the first quarter
42.9USD millionagainst 14.2 in the first quarter of 2025; company report.
Reported2026Vertex6
INF · Hardware
Vendor claim: genomes per NovaSeq X Plus run
>128genomesvendor page, not independent evidence.
Reported2026Illumina14
TRD · Trade
Fall in Illumina instrument sales in China, third quarter
54% fallyear on year; import ban lifted in November 2025.
Reported2025MedTech Dive31
3.2Domain posture
Each of the twelve coupled domains is read through genomics, in words, not scored. The coupling column names the dependency that carries genomics risk into each domain.
| Domain | Posture at baseline | Coupling | Status |
|---|---|---|---|
| WAT | Water use of sequencing laboratories and cell-therapy manufacture is not published. | none documented | Expert input EQL 1 |
| ENE | Compute for genomics has a carbon footprint; sequencing and cold-chain energy is unpublished. | ENE ↔ INF | Reported EQL 3 |
| FOO | Gene-edited plants are regulated in England and the EU; yield and uptake evidence is not bound here. | GOV → FOO | Reported EQL 3 |
| HLT | The core therapeutic coupling: one approved editing product, a case report and safety events. | the core system | Reported EQL 4 |
| BIO | Reference genomes and pangenomes describe human variation; ecological applications are not evidenced here. | DAT → BIO | Reported EQL 3 |
| CLI | Footprint at scale is not bound; no figure is used. | ENE → CLI | Expert input EQL 1 |
| INF | Sequencers, flow cells and cold chains carry the work; throughput claims come from vendors. | INF ↔ DAT | Reported EQL 2 |
| FIN | Casgevy revenue is rising from a small base; access is limited by cost and manufacturing capacity. | FIN → HLT | Reported EQL 3 |
| DAT | Reference genomes and two large biobanks; ancestry balance is uneven. | the data carrier | Reported EQL 4 |
| AIC | A genome foundation model trained on 9.3 trillion base pairs was reported in a 2025 preprint; clinical use is not evidenced here. | DAT → AIC | Reported EQL 2 |
| MIN | No documented mineral coupling at baseline; consumables and reagents are not assessed. | none documented | Expert input EQL 1 |
| TRD | Trade rules changed instrument supply in 2025 and a procurement law followed. | TRD → INF | Reported EQL 3 |
3.3Sector screens
All sixteen sectors are screened for their dependence on genomics, on the same grammar as every national edition. The evidence column describes coverage of the baseline evidence, not the performance of the sector.
| Code | Sector | Baseline evidence | Exposure to watch | Evidence coverage |
|---|---|---|---|---|
| GS-00 | Cross-system | genomics couples to health, data, trade and finance | delivery outpaces oversight | THIN |
| GS-01 | Water | water use not published | none documented | THIN |
| GS-02 | Energy | compute footprint21 | load from large compute | THIN |
| GS-03 | Food | plant editing rules2936 | regulatory divergence | PARTIAL |
| GS-04 | Health | approved therapy and phase 3 results123 | safety and access | GOOD |
| GS-05 | Finance | Casgevy revenue6 | payment of one-time therapies | PARTIAL |
| GS-06 | Development | cost barrier in low-income settings8 | widening gaps | THIN |
| GS-07 | Climate | footprint at scale not bound | energy demand | THIN |
| GS-08 | Disaster | no documented coupling | none documented | THIN |
| GS-09 | Infrastructure | sequencer and cold-chain needs14 | single-vendor dependence | THIN |
| GS-10 | Cities | no documented coupling | none documented | THIN |
| GS-11 | Biodiversity | no documented coupling | none documented | THIN |
| GS-12 | Earth observation | no documented coupling | none documented | THIN |
| GS-13 | Cyber and digital | genetic data sale in bankruptcy3238 | data protection | PARTIAL |
| GS-14 | Policy | WHO framework and national rules272936 | uneven oversight | PARTIAL |
| GS-15 | Science | strong peer-reviewed base21112 | common benchmarks | GOOD |
Notes
Numbers are the edition’s reference numbers, so a note reads the same in every chapter. The full list, with every source and its licence, is in Annex C. Annex C, references
- 2Frangoul, H. et al., Exagamglogene Autotemcel for Severe Sickle Cell Disease, New England Journal of Medicine 2024 (abstract read through the Europe PMC record; 44 treated, 30 evaluable, 29 free of crises for 12 months or more). Massachusetts Medical Society, Waltham. Observation year 2024. Accessed 2026-11-03.back
- 11Nurk, S. et al., The complete sequence of a human genome, Science 2022 (abstract read through the Europe PMC record; 3.055 billion base pairs; nearly 200 million base pairs of new sequence). American Association for the Advancement of Science, Washington. Observation year 2022. Accessed 2026-11-03.back
- 16UK Biobank Whole-Genome Sequencing Consortium, Whole-genome sequencing of 490,640 UK Biobank participants, Nature 2025 (abstract read through the Europe PMC record). Springer Nature, London. Observation year 2025. Accessed 2026-11-03.back
- 6Vertex Pharmaceuticals (ed.), Vertex Reports First Quarter 2026 Financial Results (company press release read through a wire page; Casgevy revenue USD 42.9 million against USD 14.2 million; pediatric submission completed; company statement, weak evidence). Vertex, Boston. Observation year 2026. Accessed 2026-11-03.back
- 14Illumina (ed.), NovaSeq X Series product page (vendor claims: 16 to 21 Tb per run for NovaSeq X Plus, more than 128 genomes per run, run time about 14 to 48 hours; vendor evidence, weak). Illumina, San Diego. Observation year 2026. Accessed 2026-11-03.back
- 31MedTech Dive (ed.), China to lift Illumina export ban (trade press, November 2025; listing in February 2025, import ban in March 2025, lift on 10 November 2025, instrument sales in China down 54% in the third quarter; secondary report, weak evidence). Industry Dive, Washington. Observation year 2025. Accessed 2026-11-03.back
- 21Grealey, J. et al., The Carbon Footprint of Bioinformatics, Molecular Biology and Evolution 2022 (abstract read through the Europe PMC record; a software upgrade cut one tool footprint by 73%). Oxford University Press, Oxford. Observation year 2022. Accessed 2026-11-03.back
- 29UK Parliament (ed.), Genetic Technology (Precision Breeding) Act 2023, 2023 c. 6 (contents page read; section texts not read). UK Parliament, London. Observation year 2023. Accessed 2026-11-03.back
- 36UNVERIFIED, not opened: European Parliament and Council, Regulation (EU) 2026/1388 on plants obtained by certain new genomic techniques (adopted 17 June 2026, published 26 June 2026, applies from 17 July 2028), taken from search-result summaries that differ on some dates. Official Journal of the European Union, Luxembourg. Observation year 2026. Accessed 2026-11-03.back
- 1US Food and Drug Administration (ed.), FDA approves first gene therapies to treat patients with sickle cell disease (press announcement, 8 December 2023; Casgevy uses CRISPR/Cas9, Lyfgenia a lentiviral vector; patients 12 years and older). FDA, Silver Spring. Observation year 2023. Accessed 2026-11-03.back
- 3Locatelli, F. et al., Exagamglogene Autotemcel for Transfusion-Dependent beta-Thalassemia, New England Journal of Medicine 2024 (abstract read through the Europe PMC record; 52 treated, 35 evaluable, 32 transfusion independent). Massachusetts Medical Society, Waltham. Observation year 2024. Accessed 2026-11-03.back
- 8Montano-Campos, J.F. et al., Cost-effectiveness of gene therapy for sickle cell disease in Uganda: tailoring high-income evidence to Uganda context, Gene Therapy 2026 (abstract read through the Europe PMC record). Springer Nature, London. Observation year 2026. Accessed 2026-11-03.back
- 32MedTech Dive (ed.), Anne Wojcicki bid to buy 23andMe in bankruptcy (trade press, 17 June 2025; USD 305 million bid against a USD 256 million bid; state objections; secondary report, weak evidence). Industry Dive, Washington. Observation year 2025. Accessed 2026-11-03.back
- 38UNVERIFIED, not opened: NPR (ed.), Judge approves sale of 23andMe to a nonprofit led by its founder (30 June 2025), taken from a search-result summary; the page returned a service error. NPR, Washington. Observation year 2025. Accessed 2026-11-03.back
- 27World Health Organization (ed.), Human genome editing: a framework for governance (technical document, 12 July 2021; companion recommendations published separately and not read). WHO, Geneva. Observation year 2021. Accessed 2026-11-03.back
- 12Liao, W.-W. et al. (Human Pangenome Reference Consortium), A draft human pangenome reference, Nature 2023 (abstract read through the Europe PMC record; 47 phased diploid assemblies; 119 million base pairs added). Springer Nature, London. Observation year 2023. Accessed 2026-11-03.back
