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Dante Labs

New York, New York, US

Dante Labs is transforming genetics. Our mission is to make advanced genomic testing accessible to everyone. We want to empower people with knowledge and insights about their own genetic information so that they can live healthy, long and happy lives.

Dante Labs works directly with the leading genetic labs in the United States, Europe and Asia. All of our laboratory partners are certified and have been in operation many years and process high volumes of samples on a daily basis. Thanks to the Dante Labs Network of Labs, you will access the best genetic testing technologies available worldwide.

By using only the best genetic testing technologies available worldwide, we are able to tell you everything about your genetic map. We only use Sequencing technologies (NGS and Sanger) that are the gold standard for genetic testing. Sanger is the most solid and established sequencing technology, NGS is revolutionizing healthcare and enabling personalized medicine.

Dante Labs has not listed any services.

Whole Exome Sequencing (WES)
Price on request

The Exome is the core part of the human genome that encodes proteins and provides unparalleled access to information on genetic mutations. Whole Exome Sequencing (WES) is the key to read your entire exome.

  • Average 100X Coverage
  • Raw data available upon request (free of charge)

The Exome is the core part of the human genome that encodes proteins and provides unparalleled access to information on genetic mutations. Whole Exome Sequencing (WES) is the key to read your entire exome.

  • Average 100X Coverage
  • Raw data available upon request (free of charge)
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Whole Genome Sequencing
Price on request

Your genome is your complete set of DNA. It is 3 billion letters long. Sequencing your whole genome gives you an unparalleled access to your health, your family traits, your life and much more.

  • Average 30X coverage (industry standard depth)
  • 99,7% SNP precision and sensitivity
  • Clear and insightful report
  • Raw data available (free of charge)

Your genome is your complete set of DNA. It is 3 billion letters long. Sequencing your whole genome gives you an unparalleled access to your health, your family traits, your life and much more.

  • Average 30X coverage (industry standard depth)
  • 99,7% SNP precision and sensitivity
  • Clear and insightful report
  • Raw data available (free of charge)
« Show less
Cardiac Gene Panel
Price on request

Cardiopathies are diseases of the heart. They affect the function of the heart and lead to serious illness.

Several forms of cardiomyopathies have an inherited base.

The Dante Labs Cardiopathies Panel identifies inherited gene faults that highly increase the risk of developing the most common heart diseases – that can lead... Show more »

Cardiopathies are diseases of the heart. They affect the function of the heart and lead to serious illness.

Several forms of cardiomyopathies have an inherited base.

The Dante Labs Cardiopathies Panel identifies inherited gene faults that highly increase the risk of developing the most common heart diseases – that can lead to sudden death or other serious conditions.

This test includes the following gene markers: CACNA1C, CACNA2D1, CACNB2, CASQ2, CTNNA3, DSC2, DSG2, DSP, HCN4, KCNE1, KCNE2, KCNH2, KCNJ2, KCNQ1, LMNA, MYBPC3, MYH6, MYH7, MYL2, NKX2.5, PKP2, PLN, PRKAG2, RYR2, SCN10A, SCN5A, TMEM43, TNNI3, TNNT2, TRDN, TTR

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Cystic Fibrosis Gene Panel
Price on request

Cystic fibrosis is a genetic disease that causes the body to generate thick and sticky mucus that clogs up the lungs. The digestive and the reproductive systems are also affected.

Cystic fibrosis is very common among people of Northern European ancestry.

Cystic fibrosis causes infertility in both men and women. At least 97%... Show more »

Cystic fibrosis is a genetic disease that causes the body to generate thick and sticky mucus that clogs up the lungs. The digestive and the reproductive systems are also affected.

Cystic fibrosis is very common among people of Northern European ancestry.

Cystic fibrosis causes infertility in both men and women. At least 97% of men with cystic fibrosis are infertile.

The cause of the disease is a genetic mutation in the CFTR gene that encodes for the production of a defective protein instead a healthy one.

Dante Lab Cystic Fibrosis Genetic testing will read out the CFTR gene to screen for known mutational genetic variants of well characterized gene sets.

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Targeted Cancer Gene Panel
Price on request

Cancer is the most common human genetic disease. All cancers are caused by mutations to specific genes.

Dante Labs Hereditary Cancer Test identifies gene faults inherited from parents that tremendously increase the risk of developing specific types of cancer.

This test includes the following gene markers: ATM, BRCA1, BRCA2,... Show more »

Cancer is the most common human genetic disease. All cancers are caused by mutations to specific genes.

Dante Labs Hereditary Cancer Test identifies gene faults inherited from parents that tremendously increase the risk of developing specific types of cancer.

This test includes the following gene markers: ATM, BRCA1, BRCA2, CDH1, CHEK2, NBN, PALB2, RAD51C, RAD51D, TP53, APC, BARD1, BRIP1, EPCAM, FAM175A, MLH1, MRE11A, MSH2, MSH6, MUTYH, PIK3CA, PMS2, PMS2CL, PTEN, RAD50, STK11, XRCC2

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BRCA Mutation Analysis
Price on request

BRCA1 and BRCA2 are genes called tumor suppressor that work to protect our body against cancer. Their function is to keep breast, ovarian and other cells growing normally.

Everyone has BRCA1 and BRCA2, both men and women.

When either one of these two genes is mutated, people's chance of developing breast and ovarian... Show more »

BRCA1 and BRCA2 are genes called tumor suppressor that work to protect our body against cancer. Their function is to keep breast, ovarian and other cells growing normally.

Everyone has BRCA1 and BRCA2, both men and women.

When either one of these two genes is mutated, people's chance of developing breast and ovarian cancer are greatly increased ( up to 80% for breast cancer, 60% for ovarian cancer).

Early detection of BRCA1 and BRCA2 mutations could allow the development of tailored approach and save your life.

Women with a mutated BRCA1 or BRCA2 gene also have an increased risk of developing ovarian, colon, and pancreatic cancers, as well as melanoma.

Men with an abnormal BRCA1 or BRCA2 have an higher risk of breast cancer, and an higher risk of developing prostate cancer.

About 1 in 300 people carry a BRCA1 mutation, and 1 in 800 carry a BRCA2 mutation.

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Clinical Research
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Clinical Laboratory Services
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Clinical Molecular Diagnostics
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Gene Panel Testing
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Genetic Marker Screening Services
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Biology
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Biochemistry & Molecular Biology
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Nucleic Acid Services
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DNA Services
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DNA Sequencing
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Next Generation Sequencing (NGS)
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Targeted Gene Sequencing
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Exome Sequencing Services
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