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This method is effective to detect the trend relationship of time sequences with multiple dynamic elements.
We used JM 17.2 reference software to encode the test sequences with multiple quantization parameter (QP) values.
The remaining 28 peptides were each represented in the dataset by 2 to 7 variant sequences with multiple mutations (Table S3).
We used 100 ng of cDNA for PCR amplification, and amplified all of the sequences with multiple cycle numbers (25 27 cycles) to determine the appropriate conditions for distinguishing semi-quantitative differences in expression levels.
Direct sequencing of the two nuclear genes resulted in ambiguous target sequences with multiple peaks.
Only sequences with multiple hits to retrotransposon elements were documented (Additional File 6).
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We predict 9,436 P. peruviana sequences with multiple-exon models and conserved intron positions with respect to the potato and tomato genomes.
Sequence alignments and phylogenetic analyses of the HERV-W env sequences showed that brain-derived sequences grouped with multiple HERV-W env sequences located on different chromosomes (Figure S2).
A simulated annealing approach to mixed-model sequencing with multiple objectives on a just-in-time line.
The Carr-Purcell-Meiboon-Gill pulse sequence with multiple spin echo was used for the T2 measurements.
Using bisulfite genomic sequencing with multiple clones, we selected two regions in promoters for further validation.
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