When sequencing DNA, the raw sequences that come off a machine — the "reads" — are aligned to a reference genome. Then, thee reads are traditionally stored in one of two file types: a human-readable text file of sequence data called SAM (Sequence Alignment/Map), and its binary counterpart, BAM (Binary Alignment/Map).
SAM and BAM are used throughout the genomics and health field to store genomic sequences. The highly-compressed version of BAM, CRAM, is transitioning into the field’s preferred file format for storing sequencing reads, as it reduces file size and thus storage costs.

Image summary -
Benefits
- Provides a common format to store genomic sequence read data
Target users
Researchers, and data custodians
| Title | Related Driver Projects and Organisations |
|---|---|
| Australian Genomics Data Management Systems | Australian Genomics |
Publications
| Title | Author(s) | Year |
|---|---|---|
| The Sequence Alignment/Map format and SAMtools | 2009 |
Documents
| Date | Title |
|---|---|
| 14 September 2023 | Code of Ethics and Community Conduct (CECC) |
| 11 March 2023 | Meeting minutes: File Formats |
Contributors
Don't see your name..?
Get in touch- Robert DaviesWellcome Sanger Institute (WSI), Hinxton, UK
- Richard DurbinUniversity of Cambridge, Cambridge
- Yosr HamdiInstitut Pasteur de Tunis
- Michael HoffmanPrincess Margaret Cancer Centre
- John MarshallCentre for Population Genomics
- Martin PollardWellcome Sanger Institute (WSI), Hinxton, UK