ライフサイエンスコーパス: jitter

1 the standard deviation of synaptic latency (jitter).

2 rst inter-spike interval and increased spike jitter.

3 , although there was an increase in temporal jitter.

4 amp technique), or introducing a small input jitter.

5 spectively; p = 0.011), but they had similar jitter.

6 h-frequency temporal information with little jitter.

7 into forms are quite robust to topographical jitter.

8 iest path-length differences introduce phase jitter.

9 he fundamental comb linewidth and DKS timing jitter.

10 with ultrahigh coherence and ultralow timing jitter.

11 small motion parallax cues provided by head jitter.

12 tween photon detection efficiency and timing jitter.

13 tion algoritm, and is insensitive to spatial jitter.

14 wire detectors which also feature low timing jitter.

15 lted in less-potent reduction of latency and jitter.

16 AN stimulation, and reduced the latency and jitter.

17 sion, AP duration, firing rates and temporal jitter.

18 he room was stable without drift and minimal jittering.

19 encies of 98.0% (ref. (19)), sub-3-ps timing jitter(20), sensitivity from the ultraviolet(21) to the

20 ted by a fixed (400 ms regular condition) or jittered (200/300/400/500/600 ms irregular condition) in

21 field size turns out to be a consequence of jitter across trials.

22 egradation caused by the shot-to-shot energy jitter, an optimized gun phase yields only a mild reduct

23 Additionally, jittering analysis revealed that the correlations betwee

24 nergy landscape that describes the formation jitter and allows, in principle, its generalization to a

25 epetitive stimulation at 3 Hz, and increased jitter and blocking was detected by SFEMG, confirming th

26 ltaIg3-MuSK muscle were abnormal, exhibiting jitter and blocking.

27 synaptic AP firing that minimizes both spike jitter and failures, two characteristics critically impo

28 transmission at high rates with low temporal jitter and has adapted specialized synaptic mechanisms t

29 This causes sweep-timing jitter and hence low phase stability in OCT angiography.

30 ause of high detection efficiency, sub-50-ps jitter and nanosecond-scale reset time.

31 treatment significantly increased the spike jitter and reduced the firing threshold of bushy neurons

32 ion of the fundamental frequency (F0SD), and jitter and shimmer as measured by relative average pertu

33 turbations of phonation, including increased jitter and shimmer, are associated with desiccated ambie

34 y (OPT) images, that is robust to mechanical jitter and systematic angular and spatial drift.

35 n (5-HT) through the analysis of the latency jitter and the quantal parameters: n and p in the opener

36 aboons' responses to displays that contained jittered and blurred icons suggested that their same-dif

37 In two control experiments using spatially jittered and phase-randomized stimuli, we demonstrated t

38 sical oddball effect exists even when ISI is jittered and the onset of a stimulus is not fully predic

39 , which include bump latency (mean delay and jitter) and shape (amplitude and width) variance, it is

40 ts in a loss of temporal fidelity (increased jitter) and the failure to follow high-frequency amplitu

41 is includes the maximum count rate, latency, jitter, and quantum efficiency.

42 s emittance, energy spread, spatial-pointing jitter, and shot-to-shot energy fluctuation.

43 JARs occurred even when a large artificial jitter ( approximately 60 micro;sec) was introduced to a

44 that synaptic randomness, dynamic range, and jitter are causally related.

45 tion and ICU admission rates are expected to jitter around the zero line in a long-run.

46 ough sparse, phase-lock to a stimulus with a jitter as low as 2-3 ms.

47 ty, crowding, undersampling or topographical jitter), as they also underestimated the number of featu

48 erage responses was due to different latency jitters, as confirmed with latency-corrected averages.

49 istinct periodic acoustic signal, leads to a jittered ascending temporal code, changing MGB unit resp

50 es indicated that increasing the latency and jitter at a subset of synapses reduced the number of act

51 At all ISIs tested (1 s, 3 s, or jittered at 0.8-1.2 s), deviant repetition enhanced neur

52 The trial-to-trial response jitter averaged 12 ms, a precision comparable to other s

53 umber of network metrics, including latency, jitter, bandwidth, and cost, and uses user preferences t

54 Using a novel, jitter-based measure of synchrony, we found that synchro

55 poral resolution, with negligible pump-probe jitter being possible with future laser-wakefield-accele

56 ingle-trial analysis revealed a considerable jitter between activation peaks in visual and auditory c

57 mporal pulse properties and the arrival time jitter between the FEL and optical laser pulses.

58 ample, the uncertainty--the so-called timing jitter--between the arrival of an optical trigger ('pump

59 while thin-junction devices have good timing jitter but poor efficiency.

60 erved during line-scan imaging was found to 'jitter' by +/- 0.41 microm.

61 tron bunches and the energy-dependent timing jitter can be greatly reduced to the 10 fs level.

62 ibit spontaneous oscillations with frequency jitter caused by nonequilibrium phase fluctuations.

63 aximum phonational frequency range and vocal jitter changes from baseline were significantly associat

64 e in the unadapted regions then appeared to 'jitter' coherently in random directions.

65 in volunteers with AMD under stationary and jittering conditions.

66 Transmission jitter, delay, or failures, which would corrupt the proc

67 Ten low-jitter detectors are integrated on one circuit with 100%

68 t first spike latencies and their precision (jitter) determine the onset time and precision of SLCs.

69 veral observations indicate that this visual jitter directly reflects fixational eye movements.

70 y the compensation stage, producing illusory jitter due to the undercompensation of retinal slip.

71 failure rates, and increased AP latency and jitter during high frequency repetitive firing.

72 Most minimal focal shocks activated low jitter EPSCs from single axons with characteristics rese

73 althy comparison subjects performed a rapid, jittered event-related go/no-go task.

74 scending pathway suggests that the increased jitter found in -/- MNTB responses arises mostly in the

75 sponses following a single excitation pulse, jitter-free, with fs timing precision.

76 with 2.10(-4) precision and spatial-pointing jitter from the drift mode having wide measurement span

77 A prototype of optoelectronic jitter goggles produced similar improvement in facial em

78 ansmission electron micrographs from spiral, jittered gridlike, and other partial scans.

79 ients to discriminate the facial emotions of jittering images improved by a factor of 2.

80 routines for uneven illumination and sample jitter in addition to CPU/GPU accelerated reconstruction

81 ll converge to a small value dictated by the jitter in axonal propagation times.

82 study the relationship between the temporal jitter in excitatory and inhibitory synaptic input and t

83 ynaptic inputs to a neuron and the resultant jitter in its output spike?

84 nse peaks, suggesting a decrease in temporal jitter in response to a speech signal.

85 onduction studies were normal, but increased jitter in single-fibre EMG studies indicated unstable ne

86 y account for the spike variation, while the jitter in spike timing can be primarily attributed to th

87 Given the intrinsic jitter in spike triggering, evoked synaptic potentials a

88 Thus, the timing jitter in successive layers of such neurons will converg

89 z by both the IHC receptor potential and the jitter in synaptic transmission.

90 hat is the relationship between the temporal jitter in the arrival times of individual synaptic input

91 t transient phase transitions exhibit timing jitter in the condensate formation.

92 Moreover, temporal jitter in the stimulus was transformed into a rate code

93 was employed to compensate for mass spectral jittering in MALDI data collection (e.g., peak shifts al

94 of spike occurrence, ignoring the intrinsic "jitter" in the stimulus-to-spike latency.

95 ed by calculating the standard deviation or "jitter" in the times of individual identified spikes eli

96 first-spike latency and first-spike latency jitter increased, while spontaneous and evoked firing ra

97 , inhibitory synaptic conductance, and input jitter influenced the firing rate representation of inpu

98 he electron beam energy and spatial-pointing jitter information into the mega-electron-volt ultrafast

99 We present an algorithm that takes this jitter into account.

100 tively oppose circadian synchrony and inject jitter into daily rhythms.

101 This jitter is a manifestation of the randomness associated w

102 This immunity of JAR to the EOD jitter is explained by the insensitivity of the differen

103 sub-optical-cycle and sub-femtosecond timing jitter is key to the success of many intriguing microcom

104 tances, the standard deviation in the output jitter is linearly related to the standard deviation in

105 accumulation mode, where shot-to-shot energy jitter is reduced.

106 esented in the classical oddball paradigm at jittered ISI (0.8-1.2 s), neural responses in both NCM a

107 stellate ganglion neurons with low and high jitter latencies.

108 Due to the FEL jitter, low detection efficiency of spectrometer, and lo

109 itter was 17.4 mus; 29% of neurons had spike jitter < 10 mus.

110 C latency characteristics (directly coupled, jitter < 200 micros).

111 ynaptic EPSCs identified by minimal synaptic jitter (<150 microsec) and divided into two groups: CAP-

112 Text jittering markedly enhanced word recognition speed for p

113 in the absence and presence of a temporally jittering mask.

114 m energy, energy-spread and spatial-pointing jitter monitor is experimentally verified by encoding th

115 Thus, the jittering motion of granules adjacent to the plasma memb

116 from nanoseconds to microseconds, and other "jittering" motions at timescales ranging from picosecond

117 requency of 10,000s(-1)trap(-1) and a timing jitter of +/-0.5 micros to be created.

118 occurred with a latency of 12.1 +/- 1.1 ms, jitter of 0.8-2 ms and amplitude of 57.8 +/- 7.5 pA.

119 tal comb linewidth of 100 mHz and DKS timing jitter of 1 femtosecond for averaging times up to 56 mus

120 tonic circuits and provide ultrashort timing jitter of 18 ps.

121 tal comb linewidth of 400 mHz and DKS timing jitter of 500 attosecond (averaging times up to 25 mus)

122 l neurones with a latency of 1.8 +/- 0.1 ms, jitter of 625 mus, and peak amplitude of 239 +/- 45 pA.

123 ut curve, and decreased both the latency and jitter of action potential activation.

124 lso show how chloride loading can affect the jitter of action potential timing associated with immine

125 hout constraints set by the speed and timing jitter of electronics, and should find applications rang

126 reproducible from trial to trial: the timing jitter of individual spikes was as low as 1 msec, and th

127 the LGN, identified by short latency and low jitter of LGN-evoked PSPs, showed moderate reductions in

128 ptic onset latency was much smaller than the jitter of spike response.

129 The performance is currently limited by the jitter of superconducting detectors, restricting the usa

130 icroresonators and consequently cause timing jitter of the emitted pulse trains.

131 vers instead report a clear illusory spatial jitter of the low-luminance-contrast boundary.

132 In addition, the temporal jitter of the synaptic onset latency was much smaller th

133 cteristic of expert performance (in terms of jitter of the velocity profile: Experiment 1, or through

134 -locked loop to track the resonant frequency jitter of three different resonator types one niobium ni

135 ce size of 5 mum, photon number and pointing jitters of <5% and spectral fluctuation of <10%, can be

136 instrumental artifacts such as random energy jitters of the source, signal convolution by the optical

137 roportion (0-20 of 40) and precision (0-4 ms jitter) of synchrony of inhibitory inputs, along with th

138 cterize the effect of pause length and spike jitter on the nuclear neuron firing.

139 We investigated the effect of retinal-image jitter on word recognition speed and facial emotion reco

140 e 10-150 msec range with very small temporal jitter (on the order of 1 msec).

141 n in the presence of thermal noise and clock jitter or clock skew.

142 of remarkably precise activity with very low jitter or spike count variability.

143 vs 3.6 +/- 0.3 msec; p = 0.001) but similar jitter (p = 0.57) compared with CAP-resistant neurons, r

144 What should be substantial, distracting jitter passes completely unseen.

145 temporal precision ( 100 micros arrival time jitter per mm length) and reliability: in more than 8,00

146 When jitter perception occurred, MR signal decreased in lower

147 F747S with a so far not described prominent jittering phenotype in addition to symptoms previously r

148 g changes, which may contribute to the novel jittering phenotype.

149 To confirm that high jitter, polysynaptic events were due to the presence of

150 tability by presenting temporally regular or jittered precursors, and temporal coherence by using eit

151 aximum phonational frequency range and vocal jitter predict late perceived vocal changes.

152 having wide measurement span covering energy jitter range from 10(-4) to 10(-1).

153 The jitter rate did not vary with the speed of movement.

154 We suggest that this jitter reflects a deficit in the matching of current spa

155 ovement from a single set of features: rate, jitter (regularity of rate), direction, step size, and d

156 n the near infrared regime, while the timing jitter remains 25 ps.

157 Due to a 5-fold reduced temporal jitter resulting in a shorter measurement time, the hori

158 n the second experiment, off-beat times were jittered, resulting in a similar CNV adjustment and also

159 hat presenting time-reversed, randomized, or jittered scallops increased behavioral response threshol

160 Monosynaptic EPSCs had low synaptic jitter (SD of latency to successive shocks) averaging 84

161 scallops from time-reversed, randomized, and jittered sequences.

162 P-sensitive EPSCs (n = 5) with latencies and jitter similar to those of unlabeled monosynaptic neuron

163 o other converging pathways where temporally jittered spike trains can reliably drive the downstream

164 Jittering spikes by [Formula: see text]100-500 ms, howev

165 in horizontal brainstem slices by their low-jitter, ST-evoked glutamatergic EPSCs.

166 veral response properties of C-LEPs (latency jitter, stimulus-response and perception-response functi

167 A novel illusion (visual jitter) suggests the compensation mechanism is based sol

168 cross-correlation of cell pairs, relative to jittered surrogate spike-trains, allowed us to identify

169 genetic knockout eliminated orthograde high jitter synaptic events and EPSCs evoked by retrograde ac

170 eganglionic nerve trunk, T-2, uncovered high jitter synaptic latencies consistent with polysynaptic c

171 Deeper cells displayed more latency jitter than superficial cells.

172 point data are susceptible to high-frequency jitter that clustering algorithms can mistake for transi

173 tions were improved with artificial stimulus jitter that emulated fixational eye movements, even when

174 ANF spike generation, introducing delay and jitter that limits the speed and precision of spike timi

175 ted monosynaptic IPSCs at fixed latency (low jitter) that often failed (30%) and had no frequency-dep

176 microsaccades during fixation, which rapidly jitter the "sensor" exactly when it is being voluntarily

177 al fixation, small eye movements continually jitter the location of gaze.

178 ntained both auditory and visual speech, but jittering the onset asynchrony between modalities allowe

179 By jittering the position of the bar inside the RF across t

180 ula: see text], correlates with the critical jittering time at which the toroidal topology disappears

181 These critical jittering time scales fall in the range of the periods o

182 Responses to natural images, jittered to emulate fixational eye movements, were accur

183 The results suggested that the age-degraded/jittered up-stream acoustic code may engender an increas

184 They then had "jittered" vertical grating patterns presented in their v

185 Median spike jitter was 17.4 mus; 29% of neurons had spike jitter < 1

186 ltage changes only when presynaptic temporal jitter was included.

187 The jitter was not due to small involuntary movements of the

188 The SD of the first-spike latency (jitter) was increased in VCN neurons, calyces, and MNTB

189 to impact microwave noise (and pulse timing jitter) whenever solitons radiate into dispersive waves

190 se but led to shifts in latency, or 'latency jitter', which decreased with age.

191 decrease in first spike latencies and their jitter, which could account for the intensity-dependent

192 It is important to evaluate how the FEL jitter, which is inherent in the self-amplified spontane

193 scalating the robustness of EEG data through jittering, which integrates noise into the dataset.

194 photon detection efficiency but poor timing jitter, while thin-junction devices have good timing jit

195 approaches were used to induce retinal-image jitter with duration of 100 or 166 ms and amplitude with

196 Results suggest that retinal-image jitter with optimal frequency and amplitude is an effect

197 lated to the standard deviation in the input jitter, with a constant of less than one.