Services
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Welcome to our comprehensive suite of genomic services at ATGC Bioinformatics Services. Our expert team of PhD-level professionals, with over 8 years of experience, is dedicated to advancing your research with precision and innovation. Explore our wide range of services tailored to meet your unique needs:
Project Consultation: Our experts offer in-depth project consultation to guide you through the entire research process. From conceptualization to implementation, we provide strategic insights to ensure the success of your genomic endeavors.
Genome Assembly and Annotation:
Illumina and/or Nanopore Sequencing: Leveraging cutting-edge sequencing technologies, we perform accurate and detailed genome sequencing tailored to your specifications.
De Novo, Reference-Based, Reference-Guided Assembly: Our expertise covers a variety of assembly methods, ensuring the most appropriate approach for your genomic data.
NCBI Submission: We assist in the seamless submission of your genomic data to the National Center for Biotechnology Information (NCBI).
Variant Calling: Our precise variant calling services identify genetic variations, enabling comprehensive analysis for your research needs.
Strain Identification:
16S RNA Sequencing Data and Whole-Genome Sequencing Data: We specialize in analyzing 16S RNA sequencing data and whole-genome sequencing data for accurate strain identification.
Phylogeny Creation and Pangenome Analysis: Our experts create detailed phylogenetic trees and conduct pangenome analysis to uncover evolutionary relationships among strains.
RNA Sequence Analysis:
Differential Gene Analysis: We perform in-depth analysis to identify differentially expressed genes, providing insights into gene regulation and expression patterns.
GO Term and Pathways Enrichment: Our analysis includes Gene Ontology (GO) term enrichment and pathway analysis, shedding light on biological processes and interactions.
Mechanism of Action (MOA) Generation: We unravel the intricate mechanisms of action from RNA sequencing data, offering valuable insights into gene function and regulation.
Single-Cell RNA Sequence Analysis: Leveraging the 10X Genomics platform, we analyze single-cell RNA sequencing data with precision, enabling detailed exploration of individual cell populations and their gene expression profiles.
Antibiotic Resistance Analysis: Utilising genomic and transcriptomic data, our experts conduct comprehensive analyses to identify antibiotic resistance genes and mechanisms.
Tumour Microenvironment Analysis:
TCR/BCR Data Analysis: We analyze T-cell receptor (TCR) and B-cell receptor (BCR) data, providing insights into adaptive immune responses.
Differential Gene Analysis and Immune Cell Profiling: Our analysis includes differential gene expression studies and immune cell profiling to understand the tumor microenvironment complexity.
Large Biological Data Analysis in R: Our experts specialize in R-based analysis for large biological datasets. We perform thorough comparisons and statistical analyses to validate findings and ensure scientific rigor.
Ready to embark on your genomic exploration? Book your first consultation with us, completely free of charge. Let our experts guide you toward the right services tailored to meet your research goals. Contact us today and unlock the full potential of your genomic data. Your scientific journey begins here!