---
title: Recent Posts | admin.lxlabs
---

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##### Please select your location and reference genome:

[America - GRCh37](https://us-37.congenica.com/) [America - GRCh38](https://us-38.congenica.com/) [Europe, Middle East, Africa - GRCh37](https://eu-37.congenica.com/) [Europe, Middle East, Africa - GRCh38](https://eu-38.congenica.com/)

# Latest News and Blogs

![Enabling genomic medicine](https://blog.congenica.com/hs-fs/hubfs/Congenica%20Logo%20Off%20Centre-2.jpg?width=320&height=192&name=Congenica%20Logo%20Off%20Centre-2.jpg)

 7/16/2019

#### [Enabling genomic medicine](https://blog.congenica.com/2019/07/16/enabling-genomic-medicine-the-congenica-brand-identity)

Our brand identity reflects the unique work we do and our commitment to empowering healthcare professionals to make important clinical decisions.

![Should you get your genome sequenced?](https://blog.congenica.com/hs-fs/hubfs/GATC-Sequence_2.jpg?width=320&height=192&name=GATC-Sequence_2.jpg)

 7/10/2019

#### [Should you get your genome sequenced?](https://blog.congenica.com/2019/07/10/would-you-get-your-genome-sequenced)

If you could afford it, would you get your genome sequenced? We live in exciting times, it will not be long before we are all comparing our genome data.

![Congenica named in UK life sciences – Catalysing investment and growth report](https://blog.congenica.com/hs-fs/hubfs/Global-increase_2.jpg?width=320&height=192&name=Global-increase_2.jpg)

 6/18/2019

#### [Congenica named in UK life sciences – Catalysing investment and growth report](https://blog.congenica.com/2019/06/18/congenica-named-in-uk-life-sciences-catalysing-investment-and-growth-report)

Congenica named in UK life sciences – Catalysing investment and growth report

![Improving Diagnosis for Patients with Rare Genetic Disease](https://blog.congenica.com/hs-fs/hubfs/Satellite%20Event.jpg?width=320&height=192&name=Satellite%20Event.jpg)

 6/15/2019

#### [Improving Diagnosis for Patients with Rare Genetic Disease](https://blog.congenica.com/2019/06/15/sub-event-eshg-satellite-event)

Improving Diagnosis for Patients with Rare Genetic Disease

![BGI Genomics Launch Clinical Research Whole Exome Sequencing and Interpretation Service Using Congenica Clinical Decision Support Platform](https://blog.congenica.com/hs-fs/hubfs/Loading-Sequencer_2.jpg?width=320&height=192&name=Loading-Sequencer_2.jpg)

 6/14/2019

#### [BGI Genomics Launch Clinical Research Whole Exome Sequencing and Interpretation Service Using Congenica Clinical Decision Support Platform](https://blog.congenica.com/2019/06/14/bgi-genomics-launch-clinical-research-whole-exome-sequencing-and-interpretation-service-using-congenica-clinical-decision-support-platform)

BGI Genomics Launch Clinical Research Whole Exome Sequencing and Interpretation Service Using Congenica Clinical Decision Support Platform

![Congenica supports fast, meaningful results achieved in important project](https://blog.congenica.com/hs-fs/hubfs/29156746_l_2.jpg?width=320&height=192&name=29156746_l_2.jpg)

 6/11/2019

#### [Congenica supports fast, meaningful results achieved in important project](https://blog.congenica.com/2019/06/11/congenica-supports-fast-meaningful-results-achieved-in-important-project)

Congenica supports fast, meaningful results achieved in important project

![Congenica Raises Additional £13.25M ($17.1M) to Reach Total of £23.3M ($30.1M) for Series B Funding Round](https://blog.congenica.com/hs-fs/hubfs/Money_2-1-800x533.jpg?width=320&height=192&name=Money_2-1-800x533.jpg)

 4/30/2019

#### [Congenica Raises Additional £13.25M ($17.1M) to Reach Total of £23.3M ($30.1M) for Series B Funding Round](https://blog.congenica.com/2019/04/30/congenica-raises-additional-13m-for-series-b-funding-round)

Congenica Raises Additional £13.25M ($17.1M) to Reach Total of £23.3M ($30.1M) for Series B Funding Round

![Congenica co-founder and Scientific Director Dr Matthew Hurles Elected to Fellowship of the Royal Society](https://blog.congenica.com/hs-fs/hubfs/Matt%20Hurles-1.jpg?width=320&height=192&name=Matt%20Hurles-1.jpg)

 4/18/2019

#### [Congenica co-founder and Scientific Director Dr Matthew Hurles Elected to Fellowship of the Royal Society](https://blog.congenica.com/2019/04/18/scientific-director-matthew-hurles-elected-to-fellowship-of-the-royal-society)

Congenica co-founder and Scientific Director Dr Matthew Hurles Elected to Fellowship of the Royal Society

![Congenica Announces On-Premise Deployment Option for its Genomic Analysis Platform](https://blog.congenica.com/hs-fs/hubfs/Servers_2.jpg?width=320&height=192&name=Servers_2.jpg)

 4/1/2019

#### [Congenica Announces On-Premise Deployment Option for its Genomic Analysis Platform](https://blog.congenica.com/2019/04/01/congenica-announces-on-premise-deployment-option-for-sapientia-platform)

Congenica Announces On-Premise Deployment Option for its Sapientia Platform

![Me and My Epilepsy](https://blog.congenica.com/hs-fs/hubfs/Amanda-Smith-14-400x300.jpg?width=320&height=192&name=Amanda-Smith-14-400x300.jpg)

 2/28/2019

#### [Me and My Epilepsy](https://blog.congenica.com/2019/02/28/me-and-my-epilepsy)

Me and My Epilepsy

![UK Health Minister Announces the “NHS must lead the world in genomic healthcare”](https://blog.congenica.com/hs-fs/hubfs/Nicola_Blackwood-800x533.jpg?width=320&height=192&name=Nicola_Blackwood-800x533.jpg)

 2/27/2019

#### [UK Health Minister Announces the “NHS must lead the world in genomic healthcare”](https://blog.congenica.com/2019/02/27/uk-health-minister-announces-the-nhs-must-lead-the-world-in-genomic-healthcare)

UK Health Minister Announces the “NHS must lead the world in genomic healthcare”

![Congenica Taking Deliberate Approach to International Expansion](https://blog.congenica.com/hs-fs/hubfs/International-expansion_2.jpg?width=320&height=192&name=International-expansion_2.jpg)

 11/19/2018

#### [Congenica Taking Deliberate Approach to International Expansion](https://blog.congenica.com/2018/11/19/congenica-taking-deliberate-approach-international-expansion)

Congenica Taking Deliberate Approach to International Expansion

##### Congenica is available as a CE Marked IVD clinical decision support platform for clinical diagnostic use for inherited genetic disorders in the UK and EU, Iceland, Lichtenstein, Norway, Switzerland and Turkey. In all other countries, ensuring compliance with relevant local, national and international clinical laboratory regulations is the responsibility of the laboratory.

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##### Please select your location and reference genome:

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