Geno'X · Solutions for biotech R&D

A clinician-biologist's eye on your genomic R&D

High-level medical-scientific expertise and literature intelligence for biotechs that sequence, predict and develop. I bridge your NGS/WES/WGS data and clinical reality.

The gap

Biotechs in cell therapy, gene therapy, therapeutic vaccines or drug discovery generate ever-growing volumes of sequencing data and in silico predictions. What is often missing in-house: an independent medical-scientific perspective to de-risk preclinical and translational phases, to confront algorithmic outputs with validated literature, and to anchor targets in reference clinical nomenclatures.

What I bring

  • A rare dual background. Medical biologist and next-generation sequencing specialist (NGS/WES/WGS). Few profiles bridge the gap between algorithm and clinical reality.
  • A proven, public method. genox-veille.fr is the living portfolio of my curation rigor — a weekly, scored, source-verified selection across four fields of clinical genomics.
  • A bridge to international standards. Variant and data interpretation aligned with ACMG, ClinVar, COSMIC — a skill rarely available inside startups.
  • Academic credibility. Indexed first-author publications, ORCID profile. See the author page

Three ways to work together

Scientific advisory & R&D board

For whom
Startups that want to challenge their pipelines and targets with an external medical-scientific perspective.
Format
Monthly retainer (half a day to one day per month) or a seat on your scientific committee.
Deliverable
Critical review of data pipelines through a clinical-biology lens, alerts on target consistency against medical realities.

Tailored strategic watch

For whom
Teams that must stay current with the literature, competing trials and reclassifications that directly affect their technology.
Format
Recurring subscription (monthly or quarterly).
Deliverable
An exclusive synthesis analysing the major global publications impacting your technological or therapeutic bottleneck (competing trials, new variant classifications, emerging signals).

Data curation & clinical validation

For whom
Bioinformatics / data science teams that must connect their raw results to medical-genetics references.
Format
Flexible bank of hours.
Deliverable
Expert support to translate algorithm outputs into clinical interpretation (ACMG, ClinVar, COSMIC), variant-list review, opinion on the clinical plausibility of targets.

Sample deliverables

Two thematic watch reports, so you can judge the method for yourself.

CAR-T persistence

A critical synthesis of the literature on determinants of cellular persistence, the evolution of antigenic targets and off-target risks linked to genome editing.

Request this report

AAV vector tropism

A review of AAV tissue specificity and of the pathogenic variants relevant to rare diseases of the central nervous system and the eye.

Request this report

Let's talk about your project

A project, a target or a bottleneck to explore? Describe your need in two lines — I reply within 48 hours.

Get in touch