NGS is a high throughput second generation sequencing technique used to sequence DNA and RNA accurately at a faster rate in a cost effective manner.
NBS & Metabolic Disorders
Her first test prepares her for the best! Baby screening is done using blood or urine samples for detecting Galactosemia, PKU, Congenital Hyperthyroidism, Congenital Adrenal Hyperplasia Cystic Fibrosis, Biotinidase, G6PD.
Cytogenetics is the branch of genetics dealing with chromosomal properties and its inheritance. Cytogenetics testing detects chromosomal disorders occuring due to change in number and structure of chromosomes.
Rare Genetic Disorders
A Rare disorder is a clinical condition that affects very few individuals in a general population compared to other diseases.
A simple blood test of the mother to analyse baby’s DNA to detect the risk of genetic condition in the baby.
Exome sequencing helps to identify mutations in the different genes of our DNA which may give rise to a genetic disorder.
It is used to distinguish which couples are suitable for treatment by IUI. To assess the quality of semen samples or donors for suitability.
To provide answers to cases of unexplained infertility, ART failure or repeated abortions.
Our NGS Research
Whole Exome Sequencing
Whole-genome sequencing (WGS) is a comprehensive method that uses NGS technology for analyzing the entire genome in organisms.
Whole Genome Sequencing
WGS offers interpreting the entire genome in organisms through NGS technology and bioinformatics analysis involving denovo assembly and reference based genome mapping.
Amplicon sequencing is a highly targeted approach to analyze variations in genomic regions, capture regions of interest by NGS.
Using High throughput array-based and NGS, genome-wide mapping of DNA methylation, histone modifications, chromatin accessibility, and chromosome conformation are analyzed
Mitochondrial Dna Sequencing
Mitochondrial DNA sequencing involves the sequencing of the whole mitochondrial gene for detection of any mutation or abnormalities.
Long non-coding RNA sequencing detects the non-protein coding transcripts with a length spanning over 200 nucleotides, regulating the expression of coding genes
A highly sensitive and accurate tool used for measurement of expression across the transcriptome detecting known and novel features in a single assay.
Small Rna Sequencing
Study of samples with limited number of cells or with the ultra-low amount of input RNA.
Redcliffe Genetics activately participates in prestigious conferences hosted PAN India. A Still from our participation.
I have been established with Redcliffe Genetics since last 6 months and they have provided us with great services in term of timely reporting and patient friendly pricing.
Dr. Shreyasi Sharma, MBBS
Redcliffe Genetics has supported our patients in terms of timely collection of samples and accurate reporting.
Dr. Usha Dave, Medical Geneticist & Neuroscientist
What I absolutely liked about being associated with Redcliffe Genetics is that our patient is their priority and they offer patient friendly pricing and Free Genetic Counselling both prior to and post testing.
Dr. Manju Gupta, MBBS, MS - Obstetrics & Gynaecology
The quality and consistency of Redcliffe Genetics means I can trust the results, offering best diagnosis and councelling services with affordable prices.
Dr. Sandeep Chadha, MBBS, Obstetrics & Gynaecology, Cloudnine Hospital
I highly recommend Redcliffe Genetics to others for their genetic testing. The equipments and technologies are highly versatile offered in a reasonable price in the promised time.
Dr. Ritu Mittal Arya, MBBS - Gynaecologist & Obstetrician