Sentence examples for the assembly conducted from inspiring English sources

In general, the assembly conducted with an 80% similarity criterion showed the best agreement with clusters based on marker scores (see Additional file 2, and later discussion of marker bins), indicating a tolerance for a moderate level of sequence divergence in diagnosing identical marker loci.

For P. cheesemanii these values differ slightly as the maximum number of complete coding sequences (558) was found using k-mer 41 and coverage cutoff five while the lowest number (58) was again found in the assembly conducted with coverage cutoff 19 and k-mer 63.

During its annual four-month sessions the Assembly conducted public debates.

For P. fastigiatum the highest number of complete sequences (741) was found in the assemblies conducted with k-mer 41 and with coverage cutoff seven while the lowest number (70) was found using k-mer 63 and coverage cutoff 19.

Nonetheless the N50 and N90 value as well as most other assessment parameters used do not show any significant improvement to the single assemblies conducted with ABySS.

Values for the overlap between assemblies conducted with adjacent parameters varied between 67 and 80%.

The assembly was conducted using the MIRA assembler program version 3.1.15 [ 36] with default settings and the 454 reads from the normalized, the non-normalized and the combined libraries.

The assembly was conducted with the aim of co-assembling ESTs of orthologous genes (including homoeologous pairs of genes in B. napus from each of the A and C genomes), but resolving assemblies of paralogous, or paleo-homoeologous, genes (i.e. the genes related by the ancestral genome triplication observed in diploid Brassica species).

The assembly was conducted with the aim of co-assembling ESTs of orthologous genes (including homoeologue-pairs in B. napus from each of the A and C genomes), but resolving assemblies of paralogous genes (i.e. the genes related by the ancestral genome triplication observed in Brassica species).

These assemblers are assessed based on their output quality during the assembly process conducted over fungal data.

The assembly was conducted using the default parameters.