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tool overview
On this page you find all important commands for the CLI tool ngs. If the command you are looking for is missing please ask our AI.


NGS (Next Generation Sequencing) is a command line tool used in bioinformatics for analyzing data generated by next-generation sequencing techniques. It is a powerful and flexible tool that supports a wide range of data formats and analysis methods.

NGS provides various functionalities for quality control of sequencing data, such as assessing base call quality, identifying adapter contamination, and filtering out low-quality reads. It also offers tools for read mapping, where it aligns the sequencing reads to a reference genome to identify genetic variations or study gene expression patterns.

NGS supports various types of sequencing data, including DNA-seq, RNA-seq, ChIP-seq, and ATAC-seq, enabling researchers to perform different types of genomic analyses. It can also handle paired-end sequencing data, which captures the reads from both ends of DNA fragments, providing additional information about the sequence assembly.

The tool integrates various algorithms and statistical methods for analyzing sequencing data, such as variant calling, differential gene expression analysis, peak calling for ChIP-seq data, and identifying open chromatin regions for ATAC-seq data.

NGS allows researchers to customize their analysis pipelines by combining different modules and adjusting various parameters according to their specific research questions. It also provides a scripting interface that allows users to automate tasks and efficiently process large-scale sequencing datasets.

The tool has a wide user community, which actively contributes to its development, providing updates, bug fixes, and new functionalities. It is open-source software, which means it is freely available for use and can be modified and shared by researchers.

NGS has extensive documentation, including user guides, tutorials, and examples, making it accessible to both beginners and experienced bioinformaticians. It is compatible with various operating systems, including Linux, macOS, and Windows, allowing researchers to use it on their preferred platforms.

Overall, NGS is a versatile and widely used command line tool in the field of bioinformatics, enabling researchers to analyze and interpret next-generation sequencing data for various genomics studies.

List of commands for ngs:

tool overview