Table 3.
Abundance class (Bin #) | % Binned reads in global assembly | % Binned reads from “key player” | Bin coverage (estimated by CB-Cl) | Bin coverage measured (from read mapping) | Bin size (estimated by CB-Cl) | Bin size measured (assembly length) | %Reads used in assembly of individual bins |
---|---|---|---|---|---|---|---|
Bin I | 0.2 % | 91.3 % | 581 | 656 | 6.8 Mbp | 6.5 Mbp | 91.3 % |
Bin II | 0.5 % | 1.3 % | 317 | 306 | 7.0 Mbp | 8.9 Mbp | 86.3 % |
Bin III | 1.6 % | 0.0 % | 140 | 152 | 20.4 Mbp | 21.2 Mbp | 86.2 % |
Bin IV | 49.8 % | 0.0 % | 47 | 44 | 38.9 Mbp | 37.6 Mbp | 71.4 % |
Bin V | 37.7 % | 0.0 % | 14 | 17 | 117 Mbp | 39 Mbp | 30.4 % |
Raw reads generated from a poly-aromatic hydrocarbon degrading enrichment culture [18] were assembled (with the ALLPATHS program [20]) globally on one hand, and segregated into 5 abundance classes (bins) followed by targeted assembly of reads from individual classes on the other hand. The assembly of reads with the highest coverage (Bin I) led to the reconstruction of a single 6.5 Mbp genome (key player), which is missing in the global metagenome assembly