Exome sequences were collected with a HiSeq™ 2000 sequencer (Illumina, San Diego, CA) with paired-end (2 × 100).
56 reference sequences were collected from NCBI GenBank database to represent other countries where WSSV has been identified.
For this purpose, 71 homologous pstS sequences were collected during 3 cruises conducted in March 2006, and April and July 2007.
Orthologous LTR sequences were collected along with genomic sequences (NRR) flanking each LTR sequence (similar in size to each LTR sequence; Fig. 1).
The pathogenicity-related genes of Candida albicans were selected and nucleotide sequences were collected from GenBank databases (Navarro-Garcia et al. 2001).
Two sequences were collected for each subject: one contained 322 frames for training and the other had around 400 frames for testing.
Sec-containing MsrB1 sequences were collected using TBLASTN.
Nup sequences were collected, aligned and alignments vetted as previously described [9].
Only 2 sequences were collected from each of subjects 3 and 31 in the early group.
A total of 812 combined HVRI+II sequences were collected from HVRbase (http://www.hvrbase.org) [50].
Clones with acceptable linker as well as CDS sequences were collected for distribution.
