Genetics

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There are 1,128 companies in the field of Genetics on spotfolio that produce or deliver products, that utilize or research technologies or that are otherwise engaged in topics such as Gene, Genetic, DNA, Genome, Molecular, Clinical, Sequencing, Disease .

Start-ups (167)

Early-stage companies (359)

Established companies (545)

The majority of these companies is located in the following countries.

United States (663)

United Kingdom (62)

Canada (44)

China (31)

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Kailos Genetics Kailos Genetics Inc.

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caused by an inherited gene mutation present at birth; other breast cancer diagnoses are considered sporadic, or caused by gene mutations acquired by an

considered sporadic, or not caused by an inherited, adverse change (mutation) in a gene, approximately five to ten percent of breast cancer cases are hereditary

developing cancer. With such a large number of gene variations affecting disease development, it’s easy to overlook exactly how they’re discovered. Some

reproductive organs and often have few or no symptoms during early stages of disease. To recognize Gynecologic Cancer Awareness Month this September, we summarize

results to you and your physician. How your DNA becomes a report Our clinical laboratory enriches specific DNA targets in your sample and sequences those

disease development, it’s easy to overlook... Read More Can a Genealogy DNA Test Really Tell Me if I Have Hereditary Cancer Genes? Aug 10, 2020 Huntsville

to main content Navigation toggle Kailos Genetics Search FOR PATIENTS Genetic Testing for the One and Only You At Kailos Genetics, our top priority is

ever share or sell my genetic information? Who has access to my genetic information? Kailos Genetics will never sell your genetic information. We will

Genetics Search Join Our Team Molecular Clinical Supervisor Huntsville, Alabama Kailos Genetics, a clinical laboratory located within the HudsonAlpha ...

main content Navigation toggle Kailos Genetics Search Join Our Team Molecular Clinical Supervisor Huntsville, Alabama Kailos Genetics, a clinical laboratory

decade of experience in genetic analysis utilizing our in-house, proprietary clinical assays and analytical software. Our highly qualified laboratory and analytics

main content Navigation toggle Kailos Genetics Search Press Release Intermountain Healthcare Contracts Kailos Genetics to Establish Network-Wide Pharmacogenetic

Skip to main content Navigation toggle Kailos Genetics Search Press Release Kailos Genetics Launches Assure Sentinel™ - COVID-19 Testing for Safe Workplaces

from you! We'll respond to you as quickly as possible. Get In Touch 601 Genome Way Suite 2005 Huntsville, AL 35806 +1-866-833-6865 9am - 5pm (Central

responsibilities for technology licensing, new product development and whole genome resource distribution domestic and international. Prior to joining Research

Scientific Officer PreviousNext OPPORTUNITY Open Roles Join our team. Molecular Clinical Technologist Huntsville, Alabama Kailos Genetics, a clinical

3billion

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Affordable genetic test on 7,000+ rare genetic diseases at once. Greater gene-disease spectrum behind each patient Many rare disease patients with different ...

000+ rare genetic diseases at once. Greater gene-disease spectrum behind each patient Many rare disease patients with different genetic causes share similar ...

inOrder # Help your rare patient get diagnosed Affordable genetic test on 7,000+ rare genetic diseases at once. Greater gene-disease spectrum behind each

One test to cover all genes Decoding all genes A genetic variant in a gene causes a rare genetic disease. To maximize the diagnostic yield, all DNA ...

gene causes a rare genetic disease. To maximize the diagnostic yield, all DNA sequences of 20,000 genes can be decoded by whole exome sequencing. With the

the diagnostic odyssey of rare disease patients. 3billion was founded aiming to end diagnostic odyssey of rare disease patients by comprehensive genetic ...

significant amount of time and cost that used to be required for genome interpretation, making the genome-scale rare disease genetic testing affordable for patients

the conditions specified. 1. Specimen type DNA Acceptable specimen types: - The most appropriate type: DNA extraction from peripheral venous blood samples

Affordable genetic tests on 7,000+ rare genetic diseases at once. Undiagnosed for undiscovered diseases In 2019 alone, 250 new rare genetic diseases have

Keum C, Her M, Chung WY, Kim YH, and Kim T, Annals of Clinical & Laboratory Science, 2020 Clinical and molecular spectra of BRAF-associated RASopathy Lee ...

Keum C, Ko MJ, Cheon CK, Jeon J, Choi JH, Yoo HW, Lee BH, Journal of human genetics, 2020 Diagnostic yield and clinical utility of whole exome sequencing ...

and Kim T, Annals of Clinical & Laboratory Science, 2020 Clinical and molecular spectra of BRAF-associated RASopathy Lee Y, Choi Y, Seo GH, Kim GH, Choi

research collaboration on the topics below. Clinical validation of rare disease genetic testing We support the clinical study of rare disease diagnosis by genetic

disease genetic testing. To achieve the goal, 3billion focuses on advancing genome interpretation technology by bioinformatics and machine learning. 3billion

BGI Group Shenzhen Huada Gene Technology Co., Ltd.

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diseases Prenatal testing Pre pregnancy testing Tumor Prevention Genetic Tumor Gene Detection Oseq™ of Tumor Drug Test for Personalized Medicine Clinical Nutritional ...

Universal Sequencing RNA Epigenomics Proteomics Metabonomics - Diagnostics Clinical Testing Reproductive Health Neonatal testing Women's health testing Detection

diseases Prenatal testing Pre pregnancy testing Tumor Prevention Genetic Tumor Gene Detection Oseq™ of Tumor Drug Test for Personalized Medicine Clinical Nutritional

published articles GigaScience Press GigaScience Press - Technology Disease Research Whole genome resequencing Whole Exome Sequencing Single Cell Sequencing ...

Large Platform - Research Platform Big Science - Major Projects Human Genetics Research Yanhuang Project International Thousand Human Genome Project Diabetes

published articles GigaScience Press GigaScience Press - Technology Disease Research Whole genome resequencing Whole Exome Sequencing Single Cell Sequencing

testing SIBSHIP testing Test Services Non-invasive DNA paternity testing during pregnancy Animal DNA testing - Instrument Platform Device Sequencing DNBSEQ-T7

testing SIBSHIP testing Test Services Non-invasive DNA paternity testing during pregnancy Animal DNA testing - Instrument Platform Device Sequencing DNBSEQ-T7

monogenic diseases Prenatal testing Pre pregnancy testing Tumor Prevention Genetic Tumor Gene Detection Oseq™ of Tumor Drug Test for Personalized Medicine

monogenic diseases Prenatal testing Pre pregnancy testing Tumor Prevention Genetic Tumor Gene Detection Oseq™ of Tumor Drug Test for Personalized Medicine

Universal Sequencing RNA Epigenomics Proteomics Metabonomics - Diagnostics Clinical Testing Reproductive Health Neonatal testing Women's health testing Detection

Large Platform - Research Platform Big Science - Major Projects Human Genetics Research Yanhuang Project International Thousand Human Genome Project Diabetes ...

International Thousand Human Genome Project Diabetes associated genes and mutation study International Cancer Genome Project Ancient human genome Chinese Thousand

International Thousand Human Genome Project Diabetes associated genes and mutation study International Cancer Genome Project Ancient human genome Chinese Thousand

also important to study the environmental adaptability of animals and the molecular mechanisms of their evolution to protect endangered species. 首页 Scientific

also important to study the environmental adaptability of animals and the molecular mechanisms of their evolution to protect endangered species. 首页 Scientific

Gene by Gene Ltd.

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X Ancestry about CompanyCareers Contact my account Gene By Gene News 20200430 Gene By Gene Responding to COVID-19 with Launch of Diagnostic Testing

COVID-19. Gene By Gene does not collect COVID-19 specimens. Patients suspected of having COVID-19 MUST NOT ENTER Gene By Gene’s place of business. Gene By Gene

Disease Reference Book Gene By Gene Carrier Screen Disease Reference Book 1 Table of Contents 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency 3-Methylglutaconic

(SARS-CoV-2) that causes novel coronavirus disease (COVID-19). Its intended use is for patients who meet the Centers for Disease Control and Prevention (CDC) criteria

ProvidersReturn To WorkPatient InformationNews & Media ForensicsRelationship DNA Testing Research Genetics Research OverviewWhole Genome SequencingSanger SequencingWhole

ProvidersReturn To WorkPatient InformationNews & Media ForensicsRelationship DNA Testing Research Genetics Research OverviewWhole Genome SequencingSanger SequencingWhole ...

WorkPatient InformationNews & Media ForensicsRelationship DNA Testing Research Genetics Research OverviewWhole Genome SequencingSanger SequencingWhole Exome SequencingFragile

Houston Genetic Testing Event Requisition Form Referral 11/22/2016 G E, vN E j j l GENE CARRIER S CR E E N 0Male 6. Email Address 7. Street Address

Screen provides you with information on your risk of having a baby with a genetic condition. Our carrier screening panel tests for 253 autosomal recessive

services Carrier Screening Clinical Testing Services & TestsTryptase CNV COVID-19 Testing General OverviewHealthcare ProvidersReturn To WorkPatient InformationNews

services Carrier Screening Clinical Testing Services & TestsTryptase CNV COVID-19 Testing General OverviewHealthcare ProvidersReturn To WorkPatient InformationNews

WorkPatient InformationNews & Media ForensicsRelationship DNA Testing Research Genetics Research OverviewWhole Genome SequencingSanger SequencingWhole Exome SequencingFragile

ForensicsRelationship DNA Testing Research Genetics Research OverviewWhole Genome SequencingSanger SequencingWhole Exome SequencingFragile X Ancestry products

ForensicsRelationship DNA Testing Research Genetics Research OverviewWhole Genome SequencingSanger SequencingWhole Exome SequencingFragile X Ancestry products

FACT SHEET FOR HEALTHCARE PROVIDERS Molecular Laboratory Developed Test (LDT) COVID-19 Authorized Tests Version 1.0 This Fact Sheet informs you of the

FACT SHEET FOR PATIENTS Molecular Laboratory Developed Test (LDT) COVID-19 Authorized Tests Version 1.0 You are being given this Fact Sheet because your

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infamous for their violent, and in some cases murderous, behaviour. The MAOA gene codes for the enzyme monoamine oxidase-A. It is located on the X chromosome

Archives ‘Drinker’ Gene Identified Are alcoholic habits determined by genes? A recently published study has revealed that a gene related to autism, called

Home » Resources » Archives Hirschsprung’s disease affects the large intestine in the human body. This disease is caused by missing nerve cells in certain

potential and take steps to prevent or delay a genetically predisposed disease from developing. Q Does the test have any limitations? Dtect Wellness

brand of dairy product was non-halal after it was found to contain porcine DNA. This discovery not only affects consumers of the product but also renders

genome METAGENOMICS AND METATRANSCRIPTOMICS Metagenomics is the study of DNA recovered directly from complex environmental samples while metatranscriptomics

ADVERTORIAL Understanding Your Genetic Risks for Cancer Dtect Onco genetic screening test lets you find out your genetic risks for cancer so that you can

Metatranscriptomics - Genome Analysis Bioinformatics Trait Analysis Trio Sequencing - Genetic Screening Dtect - News & Events - Press Releases - News - Newsletters

and characterise pathogen DNA from infected plants and animals, or from clinical samples - Identify alleles or variations in a genome Getting Started ...

Malaysia - Home - Services - Genome Sequencing Whole Genome Transcriptome Metagenomics and Metatranscriptomics - Genome Analysis Bioinformatics Trait

receptors (EGFRs) to block EGF attachment. Moreover, tumours with similar clinical characteristics (location, pathology, size, stage) may respond differently

susceptibility to AMD. They believe that an increased understanding of the genetics behind age-related macular degeneration would help predict those at risk

spreading to nearby bones and lymph nodes, which often leads to death. The genetics behind prostate cancer has been studied extensively over the years. Research

Malaysia - Home - Services - Genome Sequencing Whole Genome Transcriptome Metagenomics and Metatranscriptomics - Genome Analysis Bioinformatics Trait

launched in 2005 at the internationally renowned Intelligent Systems for Molecular Biology Symposium in the United States. Following several years of commercialisation

cells from the effects of chemotherapy. The new study shows that via its molecular mechanism, AEG-1 has the ability to induce chemoresistance, which is an

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