Explore a diverse range of specialized bioinformatics services designed to support research, training, and innovation in life sciences.
AuroSeqTech provides Next Generation Sequencing services for Whole Genome Sequencing, Exome Sequencing, and RNA-Seq using advanced platforms, streamlined workflows, and expert analysis to support cutting-edge research and clinical applications.
| Reference-Based Approach |
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| Quality filtering of raw reads |
| Align reads to reference genome |
| Detect variants (SNPs, indels, CNVs) |
| Structural variant detection |
| Gene prediction and annotation (based on reference) |
| Repeat and transposable element annotation |
| Genome quality assessment |
| Comparative genomics and variant interpretation |
| De Novo Approach |
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| Quality filtering of raw reads |
| Assemble genome without reference |
| Gap filling and scaffolding |
| Generate contigs and scaffolds |
| Gene prediction and functional annotation |
| Repeat and transposable element annotation |
| Detect structural variants |
| Genome quality assessment (N50, L50, BUSCO) |
| Identification of novel genomic regions |
