Hebe Genetics

Hebe Genetics was created with a vision of doing research and understand the fundamentals of Ageing. We do research in Mitochondrial Dysfunction, Telomere Length, Genomic Instability, Epigenetic Alterations, Immuno Senescence, Cellular Senescence, Sacropenia, DNA Methylation etc., We do provide Bioinformatics services like development and assistance with experimental design genetic variant detection somatic mutation detection mutation signature analysis transcriptome analysis (including miRNAs, down to single-cell resolution) structural variant analysis copy number variant analysis de novo genome assembly and annotation epigenomic (bisulfite and ChIP-seq) analysis sample tracking and database management Genomics Analysis Single Nucleotide Variants (SNV) Insertions and Deletions (Indel) Copy Number Variants (CNV) Structural Variants (SV) Somatic Mutation Identification Annotated Reporting Family Trio Analysis Pathogenicity Scoring Phenotype Relationship Epigenomics Analysis Methylation Profiling Functional Location Mapping Differentially Methylated CpGs Annotated Peak Calling Peak Visualization Motif Discovery Small RNA Expression Profile Categories of Small RNA Transcriptomics Analysis Gene Expression Alternative Splicing Novel Transcript Identification Isoform Identification Variant Annotation Single Nucleotide Variants (SNV) Fusion Gene Identification Novel Alternative Transcript Identification Differential Gene Expression (DEG) 10X scRNA Cell Ranger 10X scRNA Aggregation & Seurat Analysis 10X scRNA Trajectory Analysis Proteomics Analysis Normalized Protein Expression (NPX) Absolute Protein Quantitation (Target 48 Cytokine only) Statistical Analyses Data Visualization