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Next Generation Sequencing
Data Analysis

  • Diverse Services

    Our comprehensive services cater to a wide array of research needs, offering tailored bioinformatic analyses to drive your projects forward.

  • Data from Multiple Platform

    With expertise in computational analyses of NGS data obtained from leading platforms such as Illumina, BGI/MGI, or Ion Torrent, we ensure that your research objectives are met with precision and efficiency.

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Contact to Ask

At NextGen Solutions, we understand that each research project is unique.
That's why we offer fully customized bioinformatic analysis services tailored to your specific needs, study scope, and objectives. Leveraging state-of-the-art software and pipelines operating in a Linux environment, we accept raw sequencing data in various formats, including BCL, FASTQ, and BAM files.

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Custom Bioinformatic Analysis

Whole Genome Sequencing (WGS)

Analyzes the complete DNA sequence of an organism's genome, providing insights into genetic variations, structural rearrangements, and other genomic features.

Whole Exome Sequencing (WES)

Focuses on sequencing the protein-coding regions (exons) of the genome, allowing for cost-effective exploration of genetic variations associated with diseases or phenotypes.

Amplicon or Targeted Sequencing

Targets specific genomic regions of interest, enabling analysis of deep sequencing and accurate detection of mutations, gene expression, or microbial diversity in complex samples.

mRNA-seq

Analysis of entire transcriptome sequencing of mRNA molecules, providing valuable information about gene expression levels, alternative splicing events, and novel transcript discovery.

Small RNA-seq

seq: Anlaysis of small RNA molecules, such as microRNAs and piRNAs, shedding light on regulatory mechanisms, post-transcriptional gene regulation, and disease biomarkers.

Single-cell RNA-seq

Analyzing gene expression profiles at the single-cell level, uncovering cellular heterogeneity, lineage trajectories, and rare cell populations within complex tissues or organisms.

Histones & TFs-bound DNA-seq

Investigating DNA regions bound by histones and transcription factors, elucidating chromatin structure, epigenetic modifications, and gene regulatory networks.

ATAC-seq

Assesses chromatin accessibility by analyzing sequencing regions of open chromatin, offering insights into gene regulation, cell differentiation, and disease mechanisms.

WGBS and RRBS

Examination DNA methylation patterns at single-nucleotide resolution, facilitating epigenetic studies, identification of regulatory elements, and understanding of disease epigenetics.

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Projects

Standard Data Analysis Services

Leveraging state-of-the-art software and pipelines operating in a Linux environment, we accept raw sequencing data in various formats, including BCL, FASTQ, and BAM files. Whether you're delving into metagenomics, DNA-seq, RNA-seq, ChIP-seq, or Bisulfite-seq, our expertise covers a broad spectrum of applications. Our standard data analysis packages streamline the processing of raw sequencing data, ensuring accurate alignment, quantification, and variant calling.

  • FASTQ-TO-COUNTS: Transforming raw FASTQ files from standard RNA-seq experiments into tables with raw read counts.
  • FASTQ-TO-VCF: Processing raw FASTQ files from standard DNA-seq experiments into VCF (variant calling format) tables.
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Your Trusted Bioinformatics Analysis Partner

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It's all about Data and your needs, we're right there. In the middle performance quick.

  • info@ngsonline.org
    outreach@ngsonine.org