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We defined two sub-populations of LCRs: terminal LCRs (t-LCRs), occurring near the sequence extremities, and central LCRs (c-LCRs), positioned far from the sequence extremities.
To determine whether LCRs are equally distributed across PPI datasets, the study also investigated the distribution of LCRs within the different PPI datasets.
Low-copy repeats (LCRs) constitute 5% of the human genome.
To refine the structure and content of chromosome 22q11.2 LCRs, we applied computational analysis to dissect region-specific LCRs using publicly available sequences.
Similarly, as the number of pedestrians increase, the LCRs and AFDs of the received signal increases.
The LCRs and AFDs are normalized to the Root-Mean-Square (RMS) level.
CAST is used for detecting (and subsequently masking) low-complexity regions (LCRs) in protein sequences.
Thus, advancement in the methods used to investigate LCRs is of considerable basic and translational significance.
According to computer analyses of available sequencing data, LCRs may constitute >5% of the human genome.
Figure 11 Simulated CDFs (a), LCRs (b), and AFDs (c) of the received signal at 2.4 GHz.
With this system we measured the spectral retardance function of different types of crystal retarders as well as of LCRs.
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