PerkinElmer Genomics

Perkin Elmer Genomics

Biotechnology, 250 Industry Dr, Pittsburgh, Pennsylvania, 15275, United States, 5001-10000 Employees

perkinelmergenomics.com

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Who is PERKINELMER GENOMICS

Using an integrated omics-based approach, PerkinElmer Genomics is a global leader in genetic and genomic testing focused on rare diseases, hereditary cancer, inherited conditions, and new...

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  • 250 Industry Dr, Pittsburgh, Pennsylvania, 15275, United States Headquarters: 250 Industry Dr, Pittsburgh, Pennsylvania, 15275, United States
  • 1994 Date Founded: 1994
  • 5001-10000 Employees: 5001-10000
  • dollar-icon Revenue: $1 Million to $5 Million
  • tech-icon Active Tech Stack: See technologies

industries-icon Industry: Biotechnology

SIC SIC Code: 8011 | NAICS Code: 622110 | Show More

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PerkinElmer Genomics Org Chart and Mapping

Employees

Doug Leetch

IT Systems Support Specialist

Mohammad Hotaki

Team Lead / Associate Lab Technologist

Eric Hernandez

Customer Support Engineer

Minoshcka Irizarry

Laboratory Services Supervisor

Josie Cortes

Clinical Laboratory Technologist

Alesia Wood

Genomic Testing Consultant

Vahagn Militoysyan

Quality Assurance Engineer

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Frequently Asked Questions Regarding PerkinElmer Genomics

Answer: PerkinElmer Genomics's headquarters are located at 250 Industry Dr, Pittsburgh, Pennsylvania, 15275, United States

Answer: PerkinElmer Genomics's phone number is +18*********

Answer: PerkinElmer Genomics's official website is https://perkinelmergenomics.com

Answer: PerkinElmer Genomics's revenue is $1 Million to $5 Million

Answer: PerkinElmer Genomics's SIC: 8011

Answer: PerkinElmer Genomics's NAICS: 622110

Answer: PerkinElmer Genomics has 5001-10000 employees

Answer: PerkinElmer Genomics is in Biotechnology

Answer: PerkinElmer Genomics contact info: Phone number: +18********* Website: https://perkinelmergenomics.com

Answer: Using an integrated omics-based approach, PerkinElmer Genomics is a global leader in genetic and genomic testing focused on rare diseases, hereditary cancer, inherited conditions, and newborn screening. Our services support the full continuum of care from preconception and prenatal to neonatal, pediatric, and adult. Testing options include sequencing for targeted genes, multiple genes, the whole exome or genome, and copy number variations. Using a simple saliva or blood sample – including dried blood spot, we answer complex genetic questions that can proactively inform patient care and end the diagnostic odyssey for families.

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