Bioinformatics
services
for clinicians
Advanced Bioinformatics Services refer to specialized and cutting-edge computational solutions tailored to analyze and interpret complex biological data. These services utilize sophisticated algorithms, software, and high-performance computing to extract meaningful insights from various biological datasets, such as genomics, transcriptomics, proteomics, and metabolomics. Advanced Bioinformatics Services are instrumental in tasks like genome assembly, variant calling, functional annotation, pathway analysis, drug discovery, and personalized medicine.
They play a pivotal role in advancing our understanding of genetics, disease mechanisms, and the development of innovative treatments in the fields of biology, medicine, and biotechnology.
Whole Exome Analysis
Whole exome sequencing involves capturing and sequencing the exonic regions, providing a cost-effective approach to identify genetic variations associated with diseases or traits. Variant calling is a crucial step in whole exome analysis. It involves comparing the sequenced exome to a reference genome to identify differences or variations, such as single nucleotide polymorphisms (SNPs) or small insertions/deletions (indels). These variations can be further annotated to determine their potential impact on gene function or their association with diseases.
Germline Gene Panel Analysis
A genetic testing method focusing on specific genes linked to hereditary conditions, helping identify mutations and assess the risk of passing them to offspring.
Somatic Gene Panel Analysis
A genetic testing approach that examines mutations in a selected group of genes within an individual’s non-reproductive cells, often used in cancer diagnosis and treatment decisions.