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Individual colorspace sequences were loaded into a MySQL database from which distinct colorspace sequences were extracted.
After G50 purification, sequences were loaded on an ABI 3130XL automat (Applied Biosystems).
The sequences were loaded into a command line version of StackPACK V2.2.
Sequences were loaded into WebLogo 3 (Crooks et al, 2004) for graphical display of the alignment.
Both SlbZIP gene sequences and corresponding coding sequences were loaded into the Gene Structure Display Server (http://gsds.cbi.pku.edu.cn/) [ 74].
Nucleotide and protein sequences were loaded into BioEdit [ 59] and aligned using MUSCLE [ 60, 61] and CLUSTALW2 [ 62].
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The sequences are loaded, and the distribution of sequence lengths is displayed.
Once sequences are loaded into HMMEditor, user can view the Viterbi path of each sequence.
First, all the query and reference sequences are loaded from the input files in fasta format.
The.wig files generated from RNA sequencing were loaded and compared against the gonococcal genome, allowing visualization of sequencing reads mapped outside of the annotated genome.
The positional information of both the gene sequence and the corresponding coding sequence were loaded into the gene structure display server v2.0 (http://gsds.cbi.pku.edu.cn/) [ 44] to obtain information on the intron/exon structure.
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