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Updated: Jan 26, 2026

Amplicon Sequencing using the Long-Read Sequencing Technologies
Published on: August 29, 2025
Bazam: a rapid method for read extraction and realignment of high-throughput sequencing data
Simon P Sadedin1,2, Alicia Oshlack3,4
1Bioinformatics, Murdoch Children's Research Institute, Royal Children's Hospital, Flemington Road, Parkville, Victoria, 3052, Australia. simon.sadedin@mcri.edu.au.
Bazam efficiently extracts original FASTQ sequencing data from aligned files, enabling faster realignment. This tool significantly reduces computational time for genomic analyses and supports targeted data extraction.
Area of Science:
- Genomics
- Bioinformatics
Background:
- Short-read sequencing data is commonly stored as aligned reads.
- Aligned data can become outdated with new reference genomes and alignment methods.
Purpose of the Study:
- To introduce Bazam, a tool for extracting original paired FASTQ data from alignment files (BAM/CRAM).
- To enable efficient realignment and reduce computational time for genomic analyses.
Main Methods:
- Bazam extracts paired FASTQ reads from BAM or CRAM files.
- The extracted data is formatted for direct and efficient realignment.
Main Results:
- Bazam reduces realignment time by up to 90% compared to standard methods.
- The tool supports selective extraction of read pairs from specific genomic regions.
Conclusions:
- Bazam provides an efficient solution for updating and re-analyzing outdated alignment data.
- The tool enhances various genomic applications, including targeted analyses and structural variant calling.
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