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IGENOMIX AT ESHG 2022!

Meet us in Booth X4-770

 

IgENOMIX GIVEAWAY!

We are raffling off 5 EXOMES for whoever you want!

Come to our booth X4-770 and learn more

We are absolutly thrilled to announce that we will join the 55th annual European Human Genetics Conference that will take place in Vienna, Austria, from Saturday 11 to Tuesday June 14, 2022.

If you have the opportunity, please drop in at our Booth X4-770.  Say hello to our scientific team and find out the surprises we have for you!

Scientific Program Download useful material

IGENOMIX AT ESHG 2022!

Meet us in Booth X4-770

IgENOMIX GIVEAWAY!

We are raffling off 5 EXOMES for whoever you want!

Come to our booth X4-770 and learn more

We are absolutly thrilled to announce that we will join the 55th annual European Human Genetics Conference that will take place in Vienna, Austria, from Saturday 11 to Tuesday June 14, 2022.

If you have the opportunity, please drop in at our Booth X4-770.  Say hello to our scientific team and find out the surprises we have for you!

Scientific Program Download useful material

Igenomix Giveaway!

If you would like to take part in our GIVEAWAY and win one of the 5 EXOMES that we are raffling off, just stop by our booth X4-770 and our team will let you know how to participate.

Find out more
  • Valid only for those registered for the congress.
  • The 5 winners will be announced on June 23rd through the official Igenomix LinkedIn.
  • Legal Bases

Find out our latest news!

In Newborn Screening, early detection is key

Newborn Screening is a genetic test that analyzes 237 genes linked to more than 200 conditions

Find out more

  • Newborn screening is a mandatory public health program that offers screening and follow-up medical care to all newborns for a variety of medical conditions.
  • Igenomix Newborn Screening Test is a comprehensive genetic test that analyzes 237 genes using Next Generation Sequencing (NGS) technologies allowing a direct approach of genetic disorders to reach a rapid, accurate diagnosis.
  • In addition, this test identifies a child is a healthy carrier of any of these genetic alterations.

The goals of newborn screening are:

  • Decrease morbidity and mortality of actionable diseases by performing an early intervention to improve neonatal and long-term health outcomes.
  • Provide a universal health service of screening to all newborns.
  • Identifying screen-positive newborns
  • Diagnosing conditions
  • Communication with families
  • Referral to treatment centers
  • Follow up with long-term outcomes
  • Educating physicians and patients.

Learn more

Genetic Counsiling for your patientes 

Our geneticists provide support and guide you and your patients to choose the most appropriate technologies​ for each clinical case.

Find out more

 

GPDx Viewer

Our Viewer is a bioinformatic tool which enhances the genetic variant analysis during a diagnosis process. It provides multiple features and resources to streamline the variant classification

Watch demo!

Igenomix Giveaway!

If you would like to take part in our GIVEAWAY and win one of the 5 EXOMES that we are raffling off, just stop by our booth X4-770 and our team will let you know how to participate.

Find out more
  • Valid only for those registered for the congress.
  • The 5 winners will be announced on June 23rd through the official Igenomix LinkedIn.
  • Legal Bases

Find out our latest news!

In Newborn Screening, early detection is key

Newborn Screening is a genetic test that analyzes 237 genes linked to more than 200 conditions

Find out more

  • Newborn screening is a mandatory public health program that offers screening and follow-up medical care to all newborns for a variety of medical conditions.
  • Igenomix Newborn Screening Test is a comprehensive genetic test that analyzes 237 genes using Next Generation Sequencing (NGS) technologies allowing a direct approach of genetic disorders to reach a rapid, accurate diagnosis.
  • In addition, this test identifies a child is a healthy carrier of any of these genetic alterations.

The goals of newborn screening are:

  • Decrease morbidity and mortality of actionable diseases by performing an early intervention to improve neonatal and long-term health outcomes.
  • Provide a universal health service of screening to all newborns.
  • Identifying screen-positive newborns
  • Diagnosing conditions
  • Communication with families
  • Referral to treatment centers
  • Follow up with long-term outcomes
  • Educating physicians and patients.

Learn more

Genetic Counsiling for your patientes 

Our geneticists provide support and guide you and your patients to choose the most appropriate technologies​ for each clinical case.

Find out more

 

GPDx Viewer

Our Viewer is a bioinformatic tool which enhances the genetic variant analysis during a diagnosis process. It provides multiple features and resources to streamline the variant classification

Watch demo!

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  • Patient Journey
    • Before Pregnancy
    • IVF Process
    • Healthy pregnancy
    • After birth
  • Reproductive Health
    • Specialists
      • ERA
      • ERA insight Hub
      • ALICE
      • EMMA
      • EndomeTRIO
      • Infertility Panels
      • EMBRACE
      • PGT-A
      • PGT-A Plus
      • PGT-M
      • PGT-SR
      • CGT
      • NACE
      • Zenit
      • POC Portfolio
      • SAT
      • Newborn Screening
  • Diagnostics
  • About us
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    • About Igenomix
    • Igenomix Worldwide
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