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- C banding
- CNV
- Centromeric
- Copy number variations
- Cytogenetics
- Deletions
- Diagnóstico pré natal
- Duplications
- Dysmorphism
- Functional Genomics
- G banding
- Leucemia
- Marker chromosome
- NOR banding
- Neural development
- Neural development diseases
- Ring Chromosome
- Sub-telomerics regions
- Transcriptomics
- Unbalanced chromosome rearrengement
- Whole Chromosome Painting - WCP
- array-CGH
- hemato oncology
3 available services
Service provided byCytogenetics and Genomics Laboratory
Array-CGH
The LCG has different array resolutions in order to identify Copy number variations (CNV) and detection of loss of heterozygosity. This diagnosis can be done on pre-natal and post-natal samples.
High resolution banding karyotype
The study of the constitutional karyotype makes it possible to observe the entire genome, being able to identify both balanced and unbalanced structural chromosomal alterations, as well as alterations in the number of chromosomes and mosaics.
Molecular Cytogenetics - Fluorescence In Situ Hybridization (FISH)
Molecular cytogenetics (FISH) allows a more detailed study of specific chromosomal regions, increasing the resolving power of conventional cytogenetics. The LCG provides an extensive library of FISH probes.