Why choose BioCompin

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Our Whole Genome Sequencing service provides a comprehensive analysis of the entire genetic makeup of an organism. From variant detection to in-depth genomic insights, we deliver high-quality, accurate results tailored to your research needs. Whether you're exploring human, plant, or microbial genomes, our WGS solutions offer:

• Complete genome coverage with high depth and accuracy
• Identification of SNPs, indels, structural variants, and CNVs
• Customized bioinformatics analysis and data interpretation

Our Small RNA Sequencing service provides precise analysis of small non-coding RNAs, such as microRNAs (miRNAs) and small interfering RNAs (siRNAs), which play crucial roles in gene regulation. We offer cutting-edge sequencing solutions designed to detect and quantify these RNA molecules, enabling insights into gene expression and regulatory pathways. Our service includes:

• High sensitivity and accuracy for detecting low-abundance small RNAs
• Identification of known and novel small RNAs, including miRNAs, piRNAs, and siRNAs
• Profiling of differential expression and discovery of regulatory patterns
• Comprehensive data analysis, including alignment, annotation, and expression quantification
• Support for diverse sample types, including human, animal, and plant tissues

Our Metagenomics service offers in-depth analysis of microbial communities from various environments, enabling the study of biodiversity, ecological interactions, and functional profiles of microbiomes. Our service includes:

• Shotgun metagenomic sequencing for profiling complex microbial communities
• Identification and quantification of bacteria, viruses, fungi, and other microorganisms
• Functional analysis to uncover metabolic pathways and gene functions
• Comparative analysis of microbial communities across different samples or conditions
• High-quality bioinformatics pipelines for taxonomic classification, diversity metrics, and functional annotation

Our Transcriptome Sequencing service provides a comprehensive view of gene expression by analyzing the entire set of RNA transcripts in a cell or tissue. our service include:

• High-resolution RNA sequencing to capture coding and non-coding RNAs
• Detection of alternative splicing events, gene fusions, and novel transcripts
• Quantification of gene expression levels across different conditions or tissues

Our Metatranscriptomics Sequencing service offers a deep analysis of the active gene expression within microbial communities, providing insights into the functional roles of microorganisms in their environments. This approach captures the RNA transcripts from all the microbes present in a sample, allowing you to study community-wide gene expression and understand how microbial interactions influence ecosystem functions. our service include:

• Comprehensive profiling of active genes from complex microbial communities
• Detection of functional gene expression linked to metabolic pathways and environmental responses
• Comparative analysis of gene activity across different samples or conditions
• Taxonomic and functional annotation to identify both known and novel microbial functions

Our Structural Biology service provides detailed insights into the three-dimensional structures of biomolecules, offering a deeper understanding of their functions, interactions, and mechanisms. we help you elucidate the atomic details of proteins, nucleic acids, and complexes. Our service include: 

• Structural analysis and molecular modeling to understand mechanisms of action, binding sites, and functional conformations
•  Docking, Modelling, and Simulation service is ideal for drug discovery, biomolecular research, and protein engineering, offering computational insights 
•  Protein-protein interaction mapping to explore molecular networks and pathways 

Sanger sequencing is widely used to get high quality long read (up to 500 bp or more) targeting smaller genomic regions in a larger number of samples. 

To facilitate the submission of your sequencing data to the NCBI database, including 16S rRNA, Whole Genome Sequencing (WGS), metagenomic data, coding sequence (CDS) features, and genomic DNA