Services (Data Anaylst)
- Last Updated On :
Services :
Multi-Omics, molecular modeling and AI based data analytics services |
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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 |
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