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WHOLE GENOME SEQUENCING

Unlock the secrets of the genome with precision and efficiency

Dive into the vast expanse of genomic data.

 

From pinpointing genetic variants to unraveling complex structural variations, g.nome equips researchers with the tools to analyze the entire genome with precision and efficiency. Our platform offers advanced features for variant detection, structural variation analysis, and functional annotation, enabling researchers to gain deeper insights into genetic underpinnings and drive forward genomic research with confidence.

Identify Genetic Variants with Confidence
Accurate Variant Calling

Variant calling is essential for identifying single nucleotide variants (SNVs), insertions, deletions, and other genomic alterations. g.nome employs state-of-the-art algorithms to accurately call variants from whole genome sequencing data. 

How g.nome helps: 

  • Utilizes advanced algorithms to reduce false positive and false negative variant calls. 
  • Integrates quality filters to ensure high-confidence variant calls. 
  • Provides interactive visualizations for variant exploration and validation. 

Detect Structural Variations with Precision
CNV and Indel Analysis

Copy number variations (CNVs) and insertions/deletions (Indels) play a significant role in genomic diversity and disease. g.nome offers specialized tools to detect and analyze CNVs and Indels from whole genome sequencing data.

How g.nome helps:

  • Implements robust algorithms for accurate CNV and Indel detection. 
  • Provides visualization tools to explore CNV and Indel profiles across samples. 
  • Offers annotation databases to interpret the functional impact of detected variants. 

Explore Genetic Variants in Germline DNA
Germline Sequencing

Germline sequencing aims to uncover genetic variants inherited from parents, providing insights into inherited diseases and genetic predispositions. g.nome offers specialized pipelines and analysis tools for germline sequencing data.

How g.nome helps: 

  • Implements tailored workflows for germline variant detection and analysis. 
  • Integrates with population databases to annotate and interpret germline variants. 
  • Provides customizable reporting tools for communicating findings in research or clinical settings. 

Explore More

 

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Single-Cell RNA-seq

Explore the complexity of cellular heterogeneity and gene expression patterns at single-cell resolution, enabling deeper insights into cell types and states in diverse biological systems.

 

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Bulk RNA Sequencing

Uncover gene expression changes across entire transcriptomes, enabling the identification of biomarkers and pathways associated with diseases and therapeutic responses.

 

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Whole Exome

Focus on the protein-coding regions of the genome to identify functional variants associated with diseases, accelerating the discovery of causative mutations and potential therapeutic targets.

 

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Targeted Sequencing

Zoom in on specific genomic regions to accurately detect variants, structural variations, and somatic mutations, enabling precise analysis tailored to specific research or clinical questions.

 

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