Technologies

Novaseq 6000

offers high throughput whole genome, exome and targeted gene sequencing. 3000 GB per run. Maximum read length -250bp

Illumina Nextseq2000

offers high throughput whole genome, exome and targeted gene sequencing. 360 GB per run. approx. Maximum read length -151bp

MiSeq

offers wide range of options – 300Mb to 15Gb per run. Read lengths from 36bp to 2x300bp

AriaMx Quantitative PCR

SYBR or Taqman based – validation and target amplification

Agilent Bravo

Automated liquid handling platform – proven high-accuracy automated dispensing from 300 p to 250 μL in 96- and 384-microplates

Agilent Microarray

All applications like gene expression, aCGH ChIP- Chip, Methylation and custom microarrays

Agilent Tape station

automated, scalable, flexible- perform true end to end QC of nucleic acids

Technology platform

Novaseq 6000 offers high throughput whole genome, exome and targeted gene sequencing. 3000 GB per run. Maximum read length -250bp

Illumina Nextseq2000 offers high throughput whole genome, exome and targeted gene sequencing. 360 GB per run. approx. Maximum read length -151bp

MiSeq offers wide range of options - 300Mb to 15Gb per run. Read lengths from 36bp to 2x300bp

AriaMx Quantitative PCR SYBR or Taqman based - validation and target amplification

Agilent Bravo Automated liquid handling platform - proven high-accuracy automated dispensing from 300 p to 250 μL in 96- and 384-microplates

Agilent Microarray All applications like gene expression, aCGH ChIP- Chip, Methylation and custom microarrays

Agilent Tape station automated, scalable, flexible- perform true end to end QC of nucleic acids

Sequencing

Explore, confirm, and characterize: From individual genetic markers to entire genomes
Our suite of next-generation sequencing (NGS) platforms stands ready to power your genotyping endeavors, equipped with the requisite IT infrastructure and bioinformatics support essential for comprehensive mutation analysis. Our NGS solutions are enhanced by proprietary insights, flexible service scheduling, and expert guidance. Collaboratively, we can pinpoint the optimal sequencing approach tailored to your DNA marker project.
In addition, our laboratory facilities adhere to stringent quality standards, compliant with international standards such as ISO 15189 (NABL) and College of American Pathologists (CAP – in process), ensuring the highest quality in our services.

Explore More

We specialize in an array of advanced analyses and techniques including:

- Oncology Spatial Genomics

- Rare Diseases Disorders RT-PCR Test Analysis

- Microarray Analysis

- Metagenomics Analysis

- Bioinformatics Analysis

- R&D projects

Our offerings encompass a broad spectrum of genomic analyses, including:

- Whole Genome Sequencing

- Whole Exome Sequencing

- Transcriptome Analysis

- Spatial Genomics

- Metagenomics

- Drug Toxicity Assays

- Personalized Screening using Microarrays

- Computational Analysis on Drug Repurposing

- Pathway Analysis

- Multi-omics Analysis

- Resequencing & Variant Interpretation

ML/AL Solution

We assist healthcare and life science organizations, along with their software partners, in storing, querying, and analysing genomic, transcriptomic, and various omics data. Our objective is to facilitate the extraction of valuable insights from this data to enhance health outcomes while providing providing scalable, secure, and cost-effective solutions.

Expedited Time to Discovery
Access our extensive range of services and high-throughput offerings to process more samples, conduct complex analyses

Cost Efficiency and Performance Optimization
We continually optimize spending while building modern, scalable applications.

Global Collaboration
Partner with us to unlock the full potential of genomics data and drive impactful discoveries in healthcare and life sciences.

Biorepository Solutions

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