Inflection synthesizes all the clinical information in the EHR with genomic data and evidence-based guidance to give clinicians a comprehensive genomic care navigation system — from first encounter through long-term follow-up.
Today
Genomic testing, clinical data, consults, care plans, patient follow-up, and family communication are scattered across teams and tools. Clinicians spend time they don't have tracking down information, re-entering data, and manually assembling a view of the patient from systems that don't work together.
With Inflection
Inflection is purpose-built to put everything needed for genomic care into a single EHR environment. Once a patient is on the platform, genomic and clinical information is continuously synthesized, updated, and mapped to evidence-based next steps — creating a deeply informed map that is always ready, at every age and in any care setting.
Genomic navigation keeps the picture complete across a lifetime of care. Without it, families wait years for answers that were available from day one.
Without Genomic Navigation
Standard newborn screening; no genomic baseline established.
With Inflection
Infant receives genomic newborn screening. Results are integrated into the EHR within Inflection.
A continuously updated, layered tool the whole team can use to move from question to answer to action.
Inflection surfaces patients who would benefit from sequencing and coordinates consent and ordering — whether from a preferred external laboratory or Inflection's lab partner for rapid whole genome sequencing — right in the EHR.
All the information in the EHR is synthesized automatically, not left stranded in standalone PDFs. Your team sees the full, integrated picture, at the moment it matters.
Inflection maps the patient's complete clinical and genomic profile to evidence-based management guidelines, giving clinicians a clear, structured view of how to translate insight into action.
Care plans, specialist consults, family communication, and clinical trial options are coordinated directly in the Inflection platform. Care plans stay with the patient as the journey continues.
Whether you use an in-house lab or a preferred send-out vendor, you can order and receive results directly in the Inflection platform. No lab on board? Inflection delivers WGS testing fast, ordered and resulted right in the EHR.
Analytics, research, and operations
Inflection helps you manage a full caseload, build research cohorts, and identify improvement opportunities — all from the same clinical environment your team already uses.
Track length of stay, genomic turnaround, and diagnostic yield across your unit so you can see where days are saved and where workflow friction remains.
Surface test authorizations, documentation gaps, and payer trends so revenue cycle teams can capture the full value of genomic care.
Monitor guideline adherence, time-to-diagnosis, and outcome trends across cohorts to inform unit-level and system-level QI projects.
Build phenotype- and genotype-based cohorts directly from your live clinical data. Export de-identified sets for trials, registries, and publications.
The impact?
In NICUs running Inflection, earlier genomic answers translate directly into shorter stays, fewer redundant workups, and targeted interventions that change the trajectory for families.
$18.4K
Average avoidable cost per NICU bed per day
Baseline used in Inflection modeling. Pending final sign-off.
$12K – $36K
Observed range across reporting NICUs
Drawn from reporting partners. Pending final sign-off.
Adjust bed count to see illustrative projections. These use the same baseline as the figures above and remain subject to final finance sign-off.
NICU bed count
Additional patients impacted
~38
infants per year
Projected savings
$460,000
per year
Length of stay reduction
~125
NICU days per year
Additional genetic diagnoses
~25
per year
Assumes $18.4K per bed annualized (range $12K–$36K). Illustrative only—not a guarantee of savings.