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Data Import

Import Next-Generation Sequencing (NGS) data and feature annotations from SAM, BAM, FASTA, FASTQ, GTF, and GFF files

Import NGS data stored in different file formats such as FASTA, FASTQ, SAM, and BAM files. Read feature annotations from GTF and GFF files. Use various objects to access and manage NGS data. For instance, the BioIndexedFile object lets you efficiently access text files with nonuniform-size entries, such as sequences and annotations. Use the object to access individual entries or a subset of entries when the source file is too big to fit in memory. Use the BioMap and BioRead objects to store and manage sequence read data containing information on headers, qualities, and alignments.


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fastainfoReturn information about FASTA file
fastareadRead data from FASTA file
fastawriteWrite to file using FASTA format
fastqinfoReturn information about FASTQ file
fastqreadRead data from FASTQ file
fastqwriteWrite to file using FASTQ format
saminfoReturn information about SAM file
samsortSort SAM files
samreadRead data from SAM file
baminfoReturn information about BAM file
bamreadRead data from BAM file
bamsortSort BAM files


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BioReadContain sequence reads and their quality data
BioMapContain sequence, quality, alignment, and mapping data
BioIndexedFileAllow quick and efficient access to large text file with nonuniform-size entries
GFFAnnotationContain General Feature Format (GFF) annotations
GTFAnnotationContain Gene Transfer Format (GTF) annotations
cuffgffreadFilter and convert GFF and GTF files
cuffgtf2samConvert GTF files to SAM files


Work with Next-Generation Sequencing Data

Use BioIndexedFile objects to extract entries from large files using indices or keys, and parse data using custom functions.

Manage Sequence Read Data in Objects

Use BioMap and BioRead objects to access and manage Next-Generation Sequencing (NGS) data from various file formats, such as FASTQ, SAM, and BAM files.

Store and Manage Feature Annotations in Objects

Use GTF and GFF feature annotation objects to retrieve feature information from one or more reference sequences.

Data Formats and Databases

Access online databases and repositories using various MATLAB® functions and import data to the workspace for further analyses.

Visualize NGS Data Using Genomics Viewer App

Use the Genomics Viewer app to view NGS alignment data for single nucleotide variation in cytochrome p450 gene.

Featured Examples