Bioinformatic Service for Next Generation Sequencing

Advancements in next-generation and long-read sequencing technologies have transformed modern biological and medical research by generating unprecedented volumes of genomic data. However, extracting meaningful insights requires robust analytical strategies, advanced computational tools, and experienced bioinformaticians.

N2Jenomics Lab Pvt. Ltd. offers end-to-end bioinformatics solutions covering every stage of sequencing and microarray data analysis. Our services support data generated from a wide range of genomics platforms, ensuring accurate processing, comprehensive interpretation, and publication-ready visualizations.

Using state-of-the-art bioinformatics pipelines, advanced statistical methods, and validated computational workflows, we deliver reliable, reproducible, and high-quality analytical results tailored to your research objectives.

Our multidisciplinary bioinformatics team comprises experienced scientists with expertise in genomics, bioinformatics, computational biology, statistics, and programming. By combining customized analytical pipelines with industry-standard and open-source tools, we provide comprehensive reports, publication-quality figures, and expert interpretation that help accelerate scientific discovery and decision-making.

Whether you are conducting basic research, clinical studies, agricultural genomics, or pharmaceutical research, our bioinformatics solutions are designed to maximize the value of your sequencing and microarray data.

Service Range

N2Jenomics Pvt. Ltd.' bioinformatics services cover a wide range of genomics applications, including but not limited to genomics, transcriptomics, epigenomics, and microarray.

Genomic Data Analysis (targeted, exome and whole genome sequencing)	Metagenomics	Transcriptomic Data Analysis	Epigenomics Data Analysis	Long-Read Sequencing Data Analysis
1. Disegno in silico of gene panel	1. RNA16S sequencing	1. Sequence quality checks	1. Analysis of ChIP-Seq data (transcription factors, histones)	1. Quality Control and Error Correction
2. Sequence quality checks	2. Identification of microbial communities' composition	2. De-novo transcriptome assembly	2. Analysis of bisulfite sequencing data (Methyl-Seq)	2. Gene/Gene Isoform Expression
3. De-novo genome assembly		3. Differential expression analysis of genes, isoforms and exons	3. Differential methylation analysis in CpG and non-CpG regions	3. Novel Gene Discovery and Full-Length Isoform Identification
4. Sequence alignment versus reference genomes		4. Analysis of fusion genes, circularized RNAs and trans-splicing events	4. HiC analysis	4. De Novo Fusion Gene Detection and Fusion Isoform Expression Profiles
5. Variant calling, annotation and prioritization (single samples, matched normal-tumor pairs, family trios)		5. Detection of long non-coding RNAs		5. Allele-Specific Expression and Haplotyping
6. Gene-ontology and pathway enrichment analysis		6. Gene-ontology and pathway enrichment analysis		6. De Novo Genome Assembly
7. Analysis of CNV and large rearrangements		7. Gene expression-dependent survival analysis		7. De Novo Transcriptome Assembly
8. Clonal evolution and heterogeneity in cancer				8. Methylation Calling, Nucleosome Positioning, and Chromatin Accessibility

Choose the Analysis Package That Best Fits Your Research

• Standard Bioinformatics Analysis

Our Standard Analysis package provides high-quality processed results generated using validated bioinformatics pipelines. The deliverables include essential analytical outputs such as annotated genetic variants, differentially expressed genes with statistical metrics, identified binding sites, methylation profiles, and other experiment-specific results. This option is ideal for researchers who require reliable, processed data for their own downstream interpretation and analysis.

• Advanced Bioinformatics Analysis

Our Advanced Analysis package goes beyond data processing by providing in-depth biological interpretation and expert consultation. Our bioinformatics specialists work closely with your research objectives, customize analytical workflows, perform project-specific analyses, interpret the biological significance of the findings, and recommend the most effective methods for data visualization and presentation. We also provide publication-ready figures, comprehensive reports, and expert insights to help maximize the impact of your research.

Why Choose N2Jenomics Lab Pvt. Ltd.?

• Customized Bioinformatics Workflows tailored to your research objectives.
• Multi-Platform Expertise supporting Illumina, Ion Torrent, PacBio SMRT, Oxford Nanopore, and major microarray technologies.
• Publication-Ready Results with high-quality figures, tables, and comprehensive reports.
• Integrated Genomics Solutions combining sequencing, microarray, statistical analysis, and bioinformatics under one roof.
• Experienced Scientific Team comprising skilled bioinformaticians, computational biologists, and genomics experts.
• Fast Turnaround Time with reliable, accurate, and reproducible analytical results.
• Comprehensive Data Interpretation to help transform complex genomic datasets into meaningful biological insights.

Talk to a scientist

Want more information about our bioinformatics services or interested in bioinformatics analysis of your raw high-throughput sequencing or microarray data? Please feel free to submit a service inquiry. We are here to help!