Bioinformatics & Genomic Data Analysis
At RES Research Centre, we offer cutting-edge Bioinformatics & Genomic Data Analysis services to transform raw sequencing data into meaningful biological insights. Our bioinformatics team supports researchers in analyzing complex datasets with precision, speed, and scientific accuracy.
Our Core Services:
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Genome Assembly & Annotation
De novo and reference-based genome assembly followed by structural and functional annotation to uncover gene features, regulatory elements, and coding potential.
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Variant Calling & Mutation Analysis
Detection and interpretation of SNPs, insertions/deletions (INDELs), and other genomic variants linked to disease, evolution, or treatment response.
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Gene Expression & Pathway Analysis
Analysis of transcriptomic data (RNA-Seq) to identify differentially expressed genes (DEGs) and map them to biological pathways, regulatory networks, and functional gene sets.
We utilize powerful platforms and pipelines such as GATK, HISAT2, STAR, DESeq2, and KEGG, delivering high-quality, publication-ready results tailored to your research objectives.