Sentence examples for common gain from inspiring English sources

Hispanic engineers had not only won points with the mayor by helping retire his debt; with City Hall as the lure, they had reeled in Anglos for common gain.

Ternary signals are also used in ACELP coders [20], but it must be stressed that the ACELP model uses only one common gain for all the pulses.

For instance, [26] exploits the minimum, maximum, and average of two independent single-channel gain functions at the left and right ears to derive a common gain.

Based on a common gain function, the mean-square error is rigorously minimized jointly in the left and right ear, thereby delivering optimal noise reduction with exact binaural cue preservation of the target speech and residual noise.

Instead, we propose in this paper to conduct the entire system's design via the minimization of statistical spectral distances seen as functions of a real-valued, common gain to be applied to all channels in the frequency-domain.

Moreover, we present a new noise reduction filter based on minimum mean-square error (MMSE), which belongs to the class of common gain filters, hence being rigorous in terms of spatial cue preservation but also efficient and competitive for the acoustic noise reduction task.

We examined possible common gains and losses among the sequenced human-adapted typhoidal strains, relative to S. typhimurium LT2.

Other common observed losses include chromosomes 3, 4, 9p, 9q, 10, 13, 14, 18, and 22. Common gains include chromosomes 7 and 19.

The most common gains observed were in chromosome 1, where minimal recurrent regions in 1p33-p32.3, 1p31.3-p31.2 and 1p21.3 were gained in 58% of the samples, whereas 1q21.2-q21.3 was gained in 55% of the samples.

Onocogenic mutations in Kirsten rat-sarcoma (KRAS) occur in up to 25% of human cancers, positioning them as the most common gain-of-function mutations in human cancer.

The L858F mutation in NaV1.7 is one of the best characterized and most common gain-of-function mutations that leads to PEM and is associated with a severe phenotype (Han et al., 2007; Samuels et al., 2008; Cheng et al., 2011; Segerdahl et al., 2012).