Inocras inc.

San Diego, California

Classification

Private

Financials

Revenue & Profit

Revenue

Valuation

Valuation

Ratios

Revenue / EBITDA
$123 MM
Valuation / Revenue
$123 MM
Valuation / Employees
$123 MM
EBITDA / Revenue
$123 MM
1-Year CAGR (Revenue)
03
3-Year CAGR (Revenue)
11
1-Year CAGR (Employees)
19
3-Year CAGR (Employees)
96

People

Employee Figures

Employees

Key Executives

NameTitleSocialsEmailPhone
John DoeEmployee
--
Jane DoeEmployee
John DoeEmployee
John DoeEmployee

401K

Total Active Participants
1234
No. Participants with Account Balances
56789
Total Liabilities Start of Year
1234
Total Assets Start of Year
56789

Deals

M&A2024-03-15Completed

Seller

Founders Group

Investor Sponsors

NorthBridge PE

Deal Amount

$120M

Target Company Valuation

$1.20 MM

Techniques

Acquisition of Assets, Taken Private

Stake Tags

100%

Is PE deal

Yes

Is deal PE backed

Yes

Total Acquired

100%

Secondary Transaction2023-09-01Canceled

Target

BrightHealth Technologies

Seller

Early Investors Consortium

Investor Sponsors

--

Deal Amount

Undisclosed

Target Company Valuation

NaN

Techniques

Secondary Sale, Management Buy-out (MBO)

Stake Tags

Majority

Is PE deal

No

Is deal PE backed

Yes

Total Acquired

65%

Funding

About

About

Inocras is a biotechnology company specializing in whole genome sequencing (WGS) and AI-powered genomic interpretation for precision health applications. The platform serves patients, healthcare providers, and researchers, with a focus on oncology and rare disease diagnostics in a CAP-accredited and CLIA-certified laboratory setting. Product Breakdown Inocras offers a suite of genomic services tailored to different user groups: CancerVision: A tumor-informed, paired somatic-germline whole-genome sequencing test for solid tumor cancers. It includes target-enhanced WGS (~40-500× depth), detecting SNVs, indels, structural variants, CNVs, with analytic features such as TMB, MSI, HRD, and clinical trial matching support. Results delivered within a two-week turnaround time and backed by genetic counseling. RareVision: A comprehensive WGS test for rare disease diagnosis. Covers over 5,000 rare disease-associated genes, analyzes both coding and non-coding regions, and includes genetic counseling support. Offers detailed variant interpretation aligned with ACMG/ClinGen guidelines, delivered in approximately two weeks. MRDVision: An ultra-sensitive (1 ppm detection) whole-genome, tumor-informed circulating tumor DNA (ctDNA) assay for minimal residual disease monitoring. It requires no targeted panels and is intended for high-precision oncology applications. Research Services: End-to-end CLIA/CAP-certified sequencing services including whole-genome sequencing, bioinformatics, data curation, and advisory support for research use, designed for biopharmaceutical, academic, and biobank clients, with typical two-week turnaround.

Keywords

Keywords

Classified

Private