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Monitoring the average molecular weight for each group of 10,000 compounds generated in sequence indicates no statistically significant differences between the groups (Figure 5A).
The bridge points B2, B3 and B end are generated in sequence from B1 by (10).
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This is because the gaps generated in sequence-based alignment algorithms often do not represent real indels, especially for remote sequences.
Although only the human reference genome is considered of finished quality [ 2, 3], it is possible to compare and also use these genomes sequences as references for the alignment of reads generated in sequencing and gene expression studies.
However, each of the Pure::variants models is generated in a sequence of 4-5 steps.
We thus saved only every 1000th genotype generated in a sequence of 106 steps.
For organisms with a reference genome, reads generated in the sequencing process are usually matched to the reference sequence with a variety of alignment algorithms.
In genome browsers, figures are generated in a sequence-centered way and annotations are usually plotted below the sequence.
Table 1 summarizes the output generated in the sequencing runs.
Also shown in Table 1 is the average number of raw read pairs generated in the sequencing.
Six sequence files were generated in FASTQ format (sequence read plus quality information in Phred format); each file corresponded to the brain tissue from which the RNA originated.
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