We specialize in providing high-quality sequencing services
We will provide fast and reliable sequencing services cover DNA and RNA analysis, ranging from traditional Sanger sequencing to high-throughput Next-Generation Sequencing (NGS).
Our Sequencing Analysis Workflow
- Data Intake & QC
- Alignment & Processing
- Variant Calling /
Quantification
-
Annotation & Filtering
-
Statistical Analysis & Interpretation
- Reporting & Delivery
De novo sequencing refers to sequencing a novel genome where there is no reference sequence available for alignment. While Whole Genome Resequencing has one primary objective: to identify the differences between various individuals' genomes with that of a reference genome.
We provide full-service next-generation sequencing, which includes genomic sequencing, targeted sequencing, and DNA sequence analysis. Because of the quick turnaround time and affordability of our high-throughput sequencing technology and advanced data analysis.
- Sanger Trace File Quality Control
- Mutation & Variant Discovery
- Transcriptome Profiling & Differential Expression
- Phylogenetic & Homology Modeling
- Plasmid & Construct Validation
- Who We Work With:
Our sequencing analysis services support:
- Academic and government research labs
- Biotech and pharmaceutical companies
- Clinical diagnostics laboratories
- Agricultural genomics and animal health researchers
- Core sequencing facilities needing analysis overflow support
What to Expect From Our Sequencing Services Service
- Platform selection (Sanger or NGS) matched to your sample type and research question
- Library preparation and quality control before sequencing
- Bioinformatic analysis (alignment, variant calling, or assembly) as needed
- A report with raw sequence files plus an interpreted summary
What a Sequencing Services Result Looks Like
Note: A representative sequencing trace. Your report includes your actual sequence files and any requested downstream analysis.
Frequently Asked Questions
What is Next-Generation Sequencing (NGS)?
Sanger Sequencing is a cost-effective method for determining the nucleotide sequence of DNA. During DNA replication, Sanger sequencing selectively incorporates chain-terminating nucleotides.
Why Choose Our Sequencing Analysis Services?
- Summary
Executive Report
Raw & Processed Data Files
Publication-Ready Figures with High-resolution vector graphics for heatmaps, dendrograms, PCA plots, and chromatograms
Fast turnaround times without compromising data quality or reproducibility
What does Next-Generation Sequencing (NGS) cover?
- Bacterial Identification
- Fungal Identification
- Yeast Sequencing
- COI gene for barcoding
- Clinical Diagnostics & Genetic Testing with Sanger Sequencing
- Genotyping By Sequencing
- Single Cell DNA Sequencing
- De Novo Genome Sequencing
- Whole Genome Resequencing
- Exome Sequencing
How do I request Next-Generation Sequencing (NGS) or get a quote?
Share the technical details of your sample or project and we will provide a quotation and expected turnaround time. You can reach us on WhatsApp/call at +91 9891 179928 or email mail@allelelifesciences.com.