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All samples compared by sequencing were identical and belonged to genotype 1b.
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Methylated and unmethylated promoter CGIs were compared by sequence for average length, GC content, and ObsCpG/ExpCpG ratio.
These previous works were all based on limited sets of sequences (less than 350 proteins) compared by multiple sequence alignments.
Sorted WT, GFPlow and GFPhigh hepatocytes were compared by RNA-sequencing analysis.
When Pneumocystis from different host species are compared by DNA sequence analysis, they always differ (23, 25, 31– 31).
Fusarium isolates were compared by multilocus sequence analysis (16 ); species of Bipolaris isolates were identified by examination of the ribosomal internal transcribed spacer region (15 ).
Sequences were then compared by using BLAST with sequences available in GenBank database http://www.ncbi.nlm.nih.gov/blast/Blast.cgi.nih.gov/blast/Blast.cgi
The twenty-one GBSSI sequences were compared by multiple alignments considering the Nipponbare sequence as the reference.
All protein sequences were compared by blastp against all other protein sequences.
The resulting feline and bovine inhibitor nucleotide sequences were compared by pairwise alignment using a 2-sequence BlastN [ 28].
Using 4D BIM, different plans can be compared by visualizing the work sequences and duration of each task.
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