>Services
Services2019-02-01T13:52:05+00:00

Services

.

We use cutting-edge technology based on array-CGH and NGS, among others, to create specific designs and offer services applicable to specialties such as Gynecology, Pediatrics, Neurology, Oncology, etc…

See the application forms

TrisoNIM®

TrisoNIM®

Fetal DNA test in maternal blood for the detection of chromosomal alterations associated with Down, Edwards or Patau syndromes.
More information

ReproNIM®

ReproNIM®

A study of carriers that allows predicting a couple’s risk of transmitting certain diseases to their offspring.
More information

TromboNIM®

TromboNIM®

Genetic study of hereditary thrombophilia aimed at the identification of patients with an increased risk of developing thromboembolic disease.  
More information

KaryoNIM® Prenatal

KaryoNIM Prenatal®

Array-CGH aimed at detecting gains and losses of genomic and chromosomal regions.
More information

NIMSEQ® Prenatal

NIMSEQ® Prenatal

A solution for the sequencing of multiple genes in a single panel, for the detection of point mutations associated with defined pathologies.
More information

NGS-ExoNIM®

NGS-ExoNIM®

Is the NIMGenetics platform for complete exome sequencing.
More information

NIMSeq® Sequencing

NIMSeq® Sequencing

For the detection of point mutations associated with defined pathologies. 
More information

Array CGH-KaryoNIM®

Array CGH-KaryoNIM®

Array-CGH allows the detection of alterations in the copy number, also known as CNVs.
More information

Others Molecular Techniques

Others Molecular Techniques

NIMGenetics offers genetic study services based on different molecular biology platforms.
More information

Medical Oncology

Medical Oncology

The genomic tests obtained from the tumor samples confirm the diagnosis, allow to establish a prognosis and facilitate the selection of the treatment for each patient.
More information

Oncohematology

Oncohematology

The identification of the molecular alterations present in oncohematological diseases is essential, in many cases, to confirm the diagnosis.
More information

Familial Cancer

Familial Cancer

The identification of families with hereditary cancer allows the establishment of effective measures also in the prevention of tumors. 
More information

Autism and intellectual disability

Autism and intellectual disability

Autism spectrum disorders (ASD) and intellectual disability are neurodevelopmental disorders (NDDs).
More information

Epilepsy

Epilepsy

The genetic diagnosis of epilepsy is complex. In recent years, causal genetic alterations have been identified in a significant and growing number of cases.
More information

Neurodevelopmental disorders and polymalformative syndromes

Neurodevelopmental disorders and polymalformative syndromes

To the difficulty of the clinical diagnosis, a high genetic heterogeneity is added.
More information

Epilepsy

Epilepsy

The genetic diagnosis of epilepsy is complex. In recent years, causal genetic alterations have been identified in a significant and growing number of cases.
More information

Neurodevelopmental disorders

Neurodevelopmental disorders

To the difficulty of the clinical diagnosis, a high genetic heterogeneity is added.
More information

OncoNIM® Biomarker

OncoNIM® Biomarker

Genetic study based on the sequencing of the tumor sample that provides information on the therapeutic options based on the mutational profile.
More information

Prosigna

Prosigna

Genomic test for establishing the risk of recurrence in women with breast cancer.
More information

OncoNIM® BRCA Prevent

OncoNIM® BRCA Prevent

Study based on massive sequencing directed to the identification of mutations and to the screening of large rearrangements in the BRCA1/2 genes.
More information

NIMFISH®

NIMFISH®

The FISH technique (fluorescent in situ hybridization) is a first-choice test in numerous clinical practice contexts for the detection of possible alterations that affect a chromosome, region or gene of interest.
More information

Single Gene Sequencing

Single Gene Sequencing

The detection of sequence alterations in certain proto-oncogenes and tumor suppressor genes is routine in the clinical practice of oncological diagnosis.
More information

NGS Services

NGS Services

We offer a complete sequencing service with the highest quality standards, adapted to meet the needs of researchers.
More information

Other genomic services

Other genomic services

We provide researchers with cutting-edge technology in their genomic services (microarrays, genotyping, and FISH probes), as well as a high level of proven experience.
More information

Genomic Services for Therapy and Cell Biology

Genomic Services for Therapy and Cell Biology

NIMGenetics integrates the best and most adapted technologies for the control of cellular stability and cross-contamination in cell cultures.
More information

Find your test

Go to the Genetic Studies Search

Have not you found what you were looking for?

Contact us