Arcensus

Add Genetics to your Health. We are exclusively focussing on the currently most innovative method for genetic diagnostics, whole genome sequencing.

Arcensus is an innovative start-up healthcare company dedicated to the early medical diagnosis of all genetic diseases and dispositions. Our special expertise is the comprehensive and scientific in-depth bioinformatic pipeline analysis and handling of the resulting big data sets and their use for a better understanding of biology and medical principles. Modern healthcare systems are moving from th

e diagnosis of present medical problems towards their prevention. We will contribute to this with our international team of scientists and experts. Add genomics to your health and be our next colleague and partner.

12/05/2023

**ستكون الندوة باللغه العربية**

انضم إلينا في ندوة العلمية المميزة عبر منصة الزوم في يوم الاثنين والموافق 15 من شهر ايار-مايو الساعه 12:00 مساءًا بتوقيت اوربا/ 1:00 بتوقيت المملكة العربية السعودية.

عنوان الندوة "اهمية تسلسل الجينوم الوراثي الكامل: في إحداث ثورة في التشخيص في الطب الحديث نستكشف فيها معا أهمية تسلسل الجينوم الكامل في إحداث ثورة في التشخيص في مجال الطب الحديث"
في هذه الندوة، سيتطرق الدكتور مرتضى قيس علي، وهو باحث سريري ومراسل طبي متخصص في التشخيص الطبي المبكر للأمراض الوراثية النادرة في الطب الحديث، في أحدث التقنيات الوراثية وتأثيرها المهم في تشخيص الحالات الطبية المعقدة.

الموضوعات الرئيسية التي سيتم تغطيتها في الندوة:

مقدمة عن تسلسل الجينوم الوراثي الكامل ودوره في التشخيص الطبي

التحديات والصعوبات التي تواجه الاطباء في التشخيص السريري

نوع الطفرات المسببه للامرض الوراثية

عرض بعض الحالات المرضية التي تم تشخيصها بواسطة تسلسل الجينوم الكامل WGS

امسح الرمز أدناه ضوئيا لإضافة الحدث إلى التقويم.

12/05/2023

**The talk is in Arabic**

Join us on 15 May, 2023 at 12:00 pm (CET)/1:00 pm (KSA) for an insightful webinar where we explore the significance of Whole Genome Sequencing (WGS) in revolutionizing diagnosis within the realm of modern medicine.

In this session, Dr. Murtadha Qays Ali, a clinical scientist dedicated to early diagnosis of rare genetic disorders will delve into the cutting-edge technology of WGS and its transformational impact on diagnosing complex medical conditions.

Key topics to be covered:

• WGS and its role in diagnosing rare genetic disorders
• Challenges and limitations faced by physicians in clinical diagnosis
• Genetic variant types and their implications in developing a disease condition
• Selected interesting cases diagnosed within Arcensus using WGS

Scan the QR code to add the talk to your calendar!!

21/03/2023

Did you know that Whole Genome Sequencing (WGS) can help people with Down syndrome in several ways?
Firstly, it can provide a more accurate diagnosis and identification of the specific type of Down syndrome. WGS can detect all chromosomal abnormalities associated with Down syndrome: trisomy 21, mosaicism, and translocations.
Secondly, WGS may help researchers better understand other genetic factors contributing to Down syndrome.
Thirdly, WGS can detect other genetic variations that may co-occur with Down syndrome, providing important information about an individual's health risks and potential treatment options.
On this World Down Syndrome Day, let's spread awareness about the importance of WGS in helping individuals with Down syndrome lead healthy and fulfilling lives by providing more comprehensive diagnoses, personalised treatment plans, and a better understanding of other genetic factors that contribute to the condition.

11/03/2023

Happy World Kidney Day, everyone! Did you know that genetics plays a crucial role in kidney health? Taking advantage of Whole Genome Sequencing (WGS), nowadays, we can identify individuals at risk of developing kidney-related diseases. Thus you can take preventive actions for yourself and your family. By detecting kidney disorders early through genetic diagnostics, doctors can also develop personalised treatment plans that are tailored to the individual patient's genetic makeup. Let's spread awareness about the importance of WGS and genetics in preventing and diagnosing kidney diseases.

Arcensus remains your long-term committed partner for diagnosing kidney and kidney-related disorders.

28/02/2023

More than 80% of all rare diseases are genetic in nature. The application of genomics in the study of rare diseases has been instrumental in the discovery of new disease-causing genes and has helped advance the development of new therapeutic approaches.
This cutting-edge technology allows us to sequence an individual's entire genetic nuclear and mitochondrial code and provides a comprehensive understanding of their genetic makeup. This leads to more accurate diagnoses, enabling earlier and better treatment for patients with rare diseases.

Today, on Rare Disease Day, let's celebrate the impact of Whole Genome Sequencing and the advancements it has made in improving the lives of those affected by rare diseases. Arcensus is always identifying the best way to the fastest diagnosis of patients with genetic diseases.

13/02/2023

Did you know that Whole Genome Sequencing allows for earlier and more precise diagnoses of mitochondrial disorders?

Studies have shown that whole genome sequencing can increase the diagnostic yield for mitochondrial diseases, with reported diagnostic rates in suspected patients for more than 90%. It's important to note that the accuracy of diagnoses through whole genome sequencing is constantly improving with advances in technology and interpretation methods, especially if you are using an optimised bioinformatic pipeline as Arcensus is doing. By sequencing the mitochondrial genome with a coverage rate of 1000x, clinicians are able to identify specific mutations in the mitochondrial DNA, even with a heteroplasmic rate of less than 1%. They are then able to provide more accurate diagnoses and personalised treatment plans.

This is a prime example of how precision medicine is improving the lives of those affected by mitochondrial diseases

07/02/2023

We are happy to announce that Arcensus is organising its webinar: Repeat expansion Diseases Assessment with Whole Genome Sequencing, for you. Join the webinar and get your CME certificate / eCertificate.

During this Webinar, our Sr. Director of Bioinformatics Research, Dr. Najim Ameziane, a molecular biologist with 15+ years of experience in molecular diagnostics of hereditary diseases, will help you understand the following:

- What are repeat expansions?
- How does repeat expansion cause disease?
- Tools to detect repeat expansions.

If this has piqued your interest, please use the following link to register: http://ow.ly/9bS950MLzpW

04/02/2023

Today, on World Cancer Day, we celebrate the impact of Whole Genome Sequencing in revolutionizing cancer diagnosis. By sequencing the entire genetic code of a cancer cell, healthcare professionals can better understand the root causes and unique genetic mutations behind each individual's cancer. This breakthrough has led to more precise and effective treatments, ultimately improving patient outcomes. Let's continue pushing the boundaries of cancer research, making precision medicine a reality for all, and supporting research that brings us closer to a world without cancer.

26/01/2023

Don't miss out on the exclusive opportunity to hear our CEO and Founder, Prof. Dr. Arndt Rolfs at Arab Health Dubai this year.

Join us at the Dubai Trade centre on January 30 to discuss a new perspective in the transformation process of the healthcare industry.

24/01/2023

We are happy to announce that Arcensus is organising its webinar: "Clinical pictures of rare diseases in South Asia", for you. Join the webinar and get your eCertificate.

During this Webinar, Dr. Yun Qin, who is a dedicated clinical scientist experienced with both the pre-clinical and clinical development of novel drugs acting as a Clinical Scientist at Arcensus, will share her experience and help you understand the following:

1) Diverse populations and restricted gene flow in South Asia lead to a higher prevalence of rare diseases

2) Early and accurate diagnosis is vital for the proper management of rare diseases. This remains a key challenge in South Asia, leading to delayed treatment and poor prognosis

3) Preventive and screening programs aiming at increasing access to genetic testing will enable early diagnosis of rare diseases and, as a result, improve the management of rare diseases in South Asia

4) Whole Genome Sequencing (WGS) is the most comprehensive genetic test available for the molecular classification of genetic diseases, providing the highest diagnostic yield.

Please use the following link to register: http://ow.ly/kTFK50Mxax9

23/01/2023

Genomics allows us to identify the exact genetic mutation, which can help us prescribe specific and effective treatments that can increase the patient's overall survival rate. We can now also assess genetic susceptibility to various diseases and response to prescribed drugs. It will play a pivotal role in the transformation of the healthcare industry.
We are excited to announce that our CEO and Founder will give a presentation, "Transforming Global Healthcare in the Age of Genomics," at Arab Health in Dubai on Monday, January 30. Let's discuss the new perspective in the transformation process of the healthcare industry.

16/01/2023

Come meet us to get to know your Genome from January 30 - February 2 at Arab Health Dubai!

Arcensus team awaits you at R:F33, Rashid Hall, Dubai Expo Center.

Adresse

Goethestraße 20
Rostock
18055

Webseite

https://arcensus-diagnostics.com/

Benachrichtigungen

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