The Sanger Institute has been funded to sequence several strains of S. pneumoniae, both by traditional capillary sequencing methods and using new rapid sequencing technologies.
Please use the project specific links below to view the project specific pages for strains sequenced by traditional methods:
454/Roche GS20 and FLX. Reads were assembled into contigs using the 454 proprietary software newbler, version 1.1. Contigs generated by mapped assemblies and de novo assemblies are available below.