Services (Data Anaylst)

Multi-Omics, molecular modeling and AI based data analytics services

Whole-genome sequencing (WGS)

Metataxonomics (16S rRNA gene sequencing)

Whole-exome sequencing (WES) 

Noncoding RNA sequencing (lncRNA and circRNA)

Somatic and germline single-nucleotide variants (SNVs)

Targeted-gene sequencing/panels (TGPs)

Copy number variants (CNVs)

Microarray (Affymetrix, Agilent, and Illumina)

Single-cell RNA sequencing (scRNA-seq)

Pan-genome analysis (core genome and accessory genome)

RNA sequencing (RNA-seq)

Genome assembly (de novo and reference-based) and annotation

Gene fusions from RNA sequencing data

Phylogenetic analysis (sequence identity, wgMLST and SNP-based)

Small RNA sequencing (sRNA-seq)

Genotypic characterization of antibiotic-resistant in bacteria

Ribosome sequencing (Ribo-seq)

Gene ontology and pathway analysis (GSEA, ORA and GSVA)

Methylation sequencing (Methyl-seq)

Interaction network (generic PPI, gene-disease association, gene-miRNA)

Illumina Bead Chip Array (HumanMethylation450/EPIC)

Molecular docking and simulation

Metagenomics (whole shotgun metagenomic sequencing)

Artificial intelligence (ML-DL model) in health care