Chromosome analysis is part of cytogenetics test services, which look for structural or numerical anomalies. These services are crucial for understanding genetic abnormalities, cancer, and prenatal problems, as well as for clinical diagnostics, research, and drug development. We offer cytogenetic services that identify structural and numerical chromosomal abnormalities, such as translocations, amplifications, and micro-deletions, employing assays based on Fluorescence In-Situ Hybridization (FISH) and modified Karyotyping..

- Karyotyping Analysis
- Fluorescence In-Situ Hybridization (FISH)
- Molecular Genetics Services
- Chromosomal Microarray Analysis (CMA)

Karyotyping Analysis

Karyotyping is the process of viewing chromosomes under a microscope during the metaphase phase of cell division and organizing them into a karyogram using a standard format that includes banding patterns, size, and shape.
- Chromosomal Abnormalities
- Prenatal Testing
- Infertility and Miscarriage Analysis
- Cancer Diagnosis
- Reproductive Medicine.

Fluorescence In-Situ Hybridization (FISH)

A molecular cytogenetic approach called Fluorescence In Situ Hybridization (FISH) locates and identifies particular DNA sequences on chromosomes or inside cells using fluorescent probes. Because of its accuracy and capacity to identify particular genetic disorders, this method is frequently used in clinical diagnostics, genetic research, and oncology.

Molecular Genetics Services

A variety of laboratory methods for molecular analysis of DNA, RNA, and genetic variants are included in molecular genetics services. These services are essential for determining disease predispositions, detecting genetic illnesses, directing personalized care, and assisting with genomics research.
- DNA & RNA Sequencing
- Analysis by Real Time PCR
- Mutation and Variant Analysis
- DNA Methylation Analysis
- Genetic Disease Testing
- Cancer Genetics.

Chromosomal Microarray Analysis

A high-resolution method for identifying chromosomal abnormalities including copy number variations (CNVs) and homozygosity regions throughout the genome is called chromosomal microarray analysis, or CMA. In clinical diagnostics for genetic abnormalities, it is a commonly utilized tool, especially in cancer, pediatric, and prenatal diagnoses..

 

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Email: info@allelelifesciences.com or Whatsapp +91- 8377082003