December 22, 2014 7:24 PM ET

Health Care Technology

Company Overview of GenoLogics Life Sciences Software, Inc.

Company Overview

GenoLogics Life Sciences Software, Inc. provides laboratory information management system (LIMS) software for the management of genomics laboratory samples, tests, and results. It offers Clarity LIMS that provides workflow tracking and integration, automation for complex and mundane tasks, production ready workflows, management reporting functionality, support for regulatory compliance, and role-based interfaces for genomics and mass spec laboratories. The company also provides customer support and technical services; Application Programming Interface Community to provide customers with the opportunity to extend and customize the LIMS for their laboratory environment; and project and impleme...

4464 Markham Street

Suite 2302

Victoria, BC V8Z 7X8


Founded in 2002





Key Executives for GenoLogics Life Sciences Software, Inc.

Chief Executive Officer and Director
Vice President of Finance and Operations
Vice President of Sales
Vice President of Product Development
Compensation as of Fiscal Year 2014.

GenoLogics Life Sciences Software, Inc. Key Developments

Macrogen Selects GenoLogics' Clarity LIMS to Strengthen X-Genome and Clinical Sequencing Services

Macrogen has announced it has licensed Clarity LIMS from GenoLogics Life Sciences Software to support its whole-genome sequencing and clinical sequencing services. Clarity is GenoLogics' laboratory information management system built specifically for the needs of clinical or research genomics and mass spec laboratories to provide end-to-end sample tracking, automation, preconfigured workflows, and superior usability. Using Clarity LIMS, Macrogen plans to strengthen its support for researchers and clinical customers by automating the analysis of whole-genome sequencing and clinical sequencing services and systematically managing the strict requirements of clinical environments.

GenoLogics Enters Agreement with Illumina to Provide Laboratory Information System for HiSeq X Ten System

GenoLogics announced it has been selected by Illumina as the preferred laboratory information management system (LIMS) provider to support HiSeq X Ten sequencing system customers. Under the agreement, the companies are working closely to provide support for HiSeq X Ten whole-genome workflows and analysis pipelines, including those to be used inside of Illumina. Additionally, Illumina will be using GenoLogics' LIMS to support its collaboration with Genomics England to sequence 100,000 genomes. The agreement pairs the $1,000 genome with the preeminent laboratory information management system, further empowering the sequencing community to sequence human whole genomes.

GenoLogics Life Sciences Software Announces Support for HIPAA-covered Entities

GenoLogics Life Sciences Software announced that the 3.0 release of Clarity LIMS further supports the growing needs of genomics labs working in clinical environments, including those that are HIPAA-covered entities. This version includes cloud-based features that ensure system security and patient data privacy. In addition, the new release also provides several new features for reagent and lot tracking to further meet clinical standards. The support for HIPAA-covered entities introduced for Clarity LIMS Gold--one of the Clarity editions--ensures that patient data are secure by enlisting a private cloud within a high-security data center. The new cloud feature is governed by a Business Associate Agreement, which is a contract between GenoLogics and the clinical genomics entity, specifying exactly how the HIPAA-protected data must be stored and managed. Furthermore, setup and ongoing management of this new cloud-based feature are handled by HIPAA-trained support staff at GenoLogics. The new version also introduces new features for reagent and lot management. Reagent and lot tracking within Clarity LIMS enables laboratories to track and manage each reagent and its associated lot numbers as part of a workflow and ensures that expired reagents or non-validated reagents or lots are not being used with clinical samples.

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