M
Multigen Genetic Diseases Evaluation Center
Genetic Diagnosis and Testing for Healthcare Providers
- Founded
- Founded 2015
- Locations
- 1 location
M
Multigen Genetic Diseases Evaluation Center
Genetic Diagnosis and Testing for Healthcare Providers
- Founded
- Founded 2015
- Locations
- 1 location
About
Multigen is an international medical genetics laboratory and biotechnology center providing fast and reliable genetic diagnosis, clinical bioinformatics analysis, and genetic counseling services utilizing next-generation sequencing (NGS), Sanger sequencing, and cytogenetic techniques.
Services
3Genetic Diagnosis Testing
Provides comprehensive, fast, and high-accuracy genetic testing services including cytogenetics, molecular genetics, karyotyping, non-invasive prenatal testing (NIPT), and next-generation sequencing (NGS) to aid clinical decision making and therapy selection for genetic disorders.
Genetic Counseling Services
Delivers detailed and comprehensible genetic counseling both online and in-person for prenatal, postnatal, oncology, and rare genetic disorders to help patients and families understand genetic risks and interpret complex genetic test results.
Bioinformatics and Project Services
Executes specialized joint research projects and genetic studies across medical, forensic, and molecular biology fields, supported by clinical bioinformatics data analysis, pipeline development, and variant scoring tools.
Products
4VFGTM
Varskor
Varskor is a genomic data analysis tool designed for variant prioritization and scoring, automating the manual filtering and literature review processes for thousands of genetic variants identified through Next-Generation Sequencing (NGS).
FAST-ID® Genetic Identification Kit
FAST-ID is an advanced STR-based genetic identification kit that delivers rapid person identification from minimal DNA samples such as blood, tissue, and buccal swabs in approximately 35 minutes.
ThromboX® Mutation Detection Kit
ThromboX is a series of single nucleotide sequencing kits designed to detect genetic variations associated with hereditary thrombophilia, including FV Leiden, Protrombin, and MTHFR mutations to aid patient risk assessment.
Quick Info
- Followers
- …
- Founded
- 2015
- Operating in
- RomaniaTurkeyUnited States
- Company type
- Tech Company
- Website
Industries2
Solution Areas3
Sub Industries4
Audience
Target Industries
Not specified yet
Customer Segments
Not specified yet
Business Model
Locations1
HeadquarterHQ
Mansuroğlu mah. 1593/1 sk. No:4 D:17 (Lider Centrio, B Blok, Kat:2) Bayraklı/ İZMİR. 35535, Turkey
Recent activity
2Sep 2026
2015
Tags3
#genetics
#biotech
#diagnostics

