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Redcliffe Genetics

Redcliffe Genetics, a unit of Redcliffe Labs, is India's fastest growing Genomics and integrated research organization to provide widest range of genomics services coupled with advanced bioinformatics analysis for healthcare companies, research institutions, other public and private partnerships across the globe.

We are the only lab in South Asia with Illumina Novaseq 6000, Nanostring’s GeoMx Digital Spatial Profiler (DSP), Oxford Nanopore, Nanostring’s nCounter to measure gene expression, MGI DNB and PacBio under the same roof.

Applications & services

Whole Genome Sequencing
Amplicon Sequencing
Transcriptome Sequencing
NGS Genotyping
Whole Exome Sequencing
ChIP Sequencing
Digital Spatial Profiler
Shotgun Metagenomics
Whole Genome Bisulphite
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Departments & Research Areas

Plant Science and Research

Agriculture is the science of farming plants and animals for food, fiber, and fuel. The impact of population pressure on agricultural land and livestock towards food sufficiency is already enormous. Degradation of lands, soils and water scarcity is aggravating the existing situation. Harnessing genomics innovations in agriculture has become an absolute necessity, as it only can address and sustainably cater to these challenges such as changing environment, expanding population, and increasing demands for nutrition. As genomics becomes more widely used in agriculture, researchers and breeders are increasingly using NGS and microarray approaches to drive discoveries and advances.

Cancer Research

A wide range of mutations, epigenetic changes and gene expression alterations are known to be involved in the progression of various cancers.

NGS methods provide deep insights into the genomes of cancers as they can detect somatic variants, tumor subclones, and circulating DNA fragments with increased sensitivity. Known as well as novel genetic aberrations and gene expression changes can be uncovered using whole genome and whole exome sequencing approaches.

This way a comprehensive view of the unique mutations and genomic alterations in cancer tissue can be obtained, including those contributed by surrounding normal tissue and tumor clonality.

Human Genomics

The Human Genome Project is one of the greatest scientific feats in history. It was a landmark global scientific effort whose signature goal was to generate the first sequence of the human genome. With advances in sequencing technologies, Next-generation sequencing is becoming the primary discovery tool in human genetics.

NGS has helped in successful identification of genes that are responsible for various Mendelian diseases as well as identification of mutations that cause undiagnosed childhood genetic diseases and those that predispose individuals to more common complex diseases. Genome-wide association studies (GWASs) have been successful in identifying genomic regions that influence the risk of human complex disease as well as in variant calling and annotation studies.

Population Genetics

Sequencing the DNA or mRNA of multiple individuals of one or more species is termed as population-scale sequencing. It aims to identify genetic variation at a population level to address questions in the fields of evolutionary, agricultural and medical research.

High-throughput sequencing technologies have provided an unprecedented opportunity to study the different evolutionary forces that have shaped present-day patterns of genetic diversity.

Furthermore, with the advent of Long-read sequencing technologies, we have now reached a level of accuracy and yield that allows their application to variant detection at a scale of tens to thousands of samples.

Animal Science and Research

NGS technologies are useful for studying various aspects of animal genomics, including genotype, gene expression and regulation, and epigenetics. These approaches offer the throughput, sensitivity, and precision needed to evaluate genetic markers and discover new ones associated with traits or disease.

Moreover, an accurate view of the genetic influence on traits and diseases is crucial for breeders develop healthier and more productive livestock. NGS provides a high-resolution view of the genetic variation influencing phenotype in animals which s useful for discovering novel markers..

Microarrays offer a cost-effective solution for analyzing large sample numbers in routine screening applications.

Client Testimonials

Dr. Rajendar Singh 
Senior Principal Scientist, Endocrinology- CDRI Understanding genetic causes of male infertility

I was happy with the services and support provided by Redcliffe for methylation sequencing. The bioinformatic team was very supportive and catered to all the requirements of my project appropriately.

Prof. Ashwani Pareek 
Executive Director- NABI Plant Biologist

I deployed services from Redcliffe for RNA Sequencing in plant samples and was quite content with the data quality. They assured highest quality standards throughout the process and paid utmost attention to timely delivery of my data.

Dr. Pavan Jutur 
Group Leader - ICGEB Omics of Algae

Most competitive prices for WGS with high quality data and excellent bioinformatic support.

Prof. Ashutosh Haldar 
Head, Department of Reproductive Biology- AIIMS Human methylation, SNP genotyping

Reliable data quality, fast turn around time and affordable pricing. I am happy to have worked with Redcliffe genetics for Whole Genome Bisulfite Sequencing as I am satisfied with the data analysis and bioinformatic support.

Prof. Gyaneshwar Chaubey 
Department of Zoology, BHU Population Genetics- Human Genome

I have worked closely with Redcliffe Genetics for a few projects in my lab and have been impressed with the quality of their services. From sample collection to data delivery, they provide constant support and make sure good quality data is delivered. They have been supportive and participated at various conferences at BHU and we have gained trust of various researchers in our university.

Prof. Rajiva Raman
Department of Zoology, BHU Molecular cytogenetics and Human Genetics

My association with Redcliffe Genetics team for WGS of Lizard samples has been really fruitful. Right from technical discussion to data analysis they have provided remarkable support and delivered quality data.

Dr. Neeraj Rai
Scientist- Birbal Sahni Institute of Palaeosciences Archaeogenetics

I work on some very difficult-to-deal with samples and was quite impressed with the data quality delivered by Redcliffe team for sequencing of all Human ancient DNA samples. I would continue my association for future projects as well.

Dr. S.P. Dixit
ICAR- NBAGR Animal Genetics

One of the most hard working and customer satisfaction-oriented research company. Data quality is their utmost priority. I work with bovine samples and was impressed with their sample handling capacity for Genotyping.

Dr. Anupama Mukherjee
Scientist- ICAR-NDRI Cattle research

Data analysis and turn-around-time are two very important parameters for sequencing services. Redcliffe delivered both satisfactorily at an affordable price.

Dr. Rahul Mahajan
Associate Prof.- PGIMER, Chandigarh Clinical Immunology

A reliable and supportive company with good pricing for Whole Exome sequencing in human samples.

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