Explore Inherited Variants with Confidence
Germline Sequencing Analysis
How g.nome helps:
- Implements robust algorithms for germline variant calling and annotation.
- Provides integration with population databases to interpret the frequency and clinical significance of germline variants.
- Offers customizable reporting features for communicating findings in research or clinical settings.
Uncover Genetic Variants with Accuracy
Precise Variant Calling
Variant calling in whole exome sequencing identifies genetic variants within the protein-coding regions of the genome. g.nome utilizes advanced algorithms to accurately call variants, including single nucleotide variants (SNVs) and small insertions/deletions (Indels).
How g.nome helps:
- Implements high-sensitivity variant calling algorithms to detect rare variants.
- Offers quality filters and annotation tools to prioritize clinically relevant variants.
- Provides visualization tools for variant exploration and validation.
Unveil Somatic Mutations with Precision
Somatic Sequencing Analysis
Somatic sequencing identifies genetic mutations specific to tumor cells, providing insights into cancer biology and personalized treatment strategies. g.nome offers specialized pipelines and analysis tools for somatic variant detection and interpretation.
How g.nome helps:
- Implements tailored workflows for somatic variant detection and filtering.
- Integrates with cancer databases and annotation tools for variant interpretation.
- Provides customizable reporting features for communicating findings in research or clinical settings.
Detect Structural Variations with Precision
CNV and Indel Analysis
Copy Number Variations (CNV) and Indel analysis in whole exome sequencing identifies structural variations such as gene duplications, deletions, and small insertions/deletions. g.nome offers specialized tools to accurately detect and analyze CNVs and Indels from exome sequencing data.
How g.nome helps:
- Utilizes robust algorithms for accurate CNV and Indel detection within exonic regions.
- Provides customizable visualization tools for exploring CNV and Indel profiles.
- Integrates annotation databases to interpret the functional impact of detected variants.
BREAK THROUGH BARRIERS WITH
