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1 did not actually have a retinal detachment (false-positive).
2 number of pharmaceuticals (22) with only one false positive.
3 ptamers, and viral RNA domains with a single false positive.
4 tients were culture negative and potentially false positive.
5 re packages reported a substantial number of false positives.
6 de of tRNA space and flags them as candidate false positives.
7 pped to a reference genome to further reduce false positives.
8 lytical thinking increases the prevalence of false positives.
9 tudies and have a higher likelihood of being false positives.
10 ography (LDCT) screening, may greatly reduce false positives.
11 detecting known strong interactions with no false positives.
12 itives, but also by decreasing the number of false positives.
13 se additional flagged features were verified false positives.
14 y 2.2% of MARGI-identified interactions were false positives.
15 se new algorithms detect significantly fewer false positives.
16 drug-target pairs, which introduces a lot of false-positives.
17 out any matrix effect, cross-reactivity, and false-positives.
18 he later progressive diseases on CT, with no false-positives.
20 treatment cases were more likely to be Xpert false-positive (45/321 Xpert-positive retreatment cases
23 an-assay interference compounds (PAINS) with false-positive activities in assays often propagate thro
24 ercent identity, can reduce the frequency of false-positive alignments more than 20-fold compared wit
25 86% specific for cardiac ATTR amyloid, with false positives almost exclusively from uptake in patien
26 46% of Xpert-positives with CT> 30 would be false positive, although 70% of false positives would be
27 ties than traditional LC-MS/MS, produced one false positive and did not detect 6 confirmed compounds.
28 which we show are partly responsible for the false positive and false negative compound identificatio
34 still suffers from non-negligible numbers of false positive and negative SNV and INDEL calls that wer
35 uspicious nodules may be helpful in avoiding false positives and altering the extent of treatment whe
36 e found TIN adjustment had better control of false positives and false negatives (sensitivity = 0.89,
37 d fair-to-poor correlation, with evidence of false positives and false negatives in the microarray da
38 enging to develop; attenuating the number of false positives and false negatives under high-throughpu
39 These results show that snoReport 2.0 avoid false positives and false negatives, allowing to predict
40 utralize RNA degradation effects by reducing false positives and recovering biologically meaningful p
43 with a statistical method that accounts for false-positive and false-negative errors to test deer sa
44 calculation of true-positive, true-negative, false-positive and false-negative patients as classified
45 wever, for gelatin, problems associated with false-positive and false-negative results, inconsistenci
46 n, technical parameters, number of true- and false-positive and true- and false-negative results were
47 nability to multiplex targets, high rates of false positives, and (in some cases) the requirement of
48 the confidence in calls, reduce the risk of false positives, and help characterize complex events.
49 of the analysis or produce broad impact eQTL false positives, and the tendency of methods that accoun
50 nning with an over-motivated state with many false positives, and transitioning through a more or les
52 atched spectra in spite of potential risk of false positive annotations emerging from automation.
54 gy for these purposes because the chances of false positives are small owing to the use of a mass spe
58 be predicted at a threshold of 0.34 without false positives at a sensitivity of 56% at 12 hours afte
63 tion sequencing (NGS) data is susceptible to false positive calls due to sequencing, mapping and othe
64 ble efforts in predicting VC concordance and false positive calls in low-concordance regions which un
65 next generation sequencing can help diminish false positive calls, but this does not ameliorate poten
70 minations identified 42.9% (39 of 91) of the false-positive cases to be the same lesion as the IBC.
74 est statistics was simulated for the desired false positive control to avoid excess false positives w
77 lects fewer invasive pneumonias versus fewer false-positive diagnoses due to less secretions and/or l
78 Outcomes included number of infants with false-positive diagnoses linked to ART per 1,000 ART ini
83 tory testing, 128/1,000 ART initiations were false-positive diagnoses; with confirmatory testing, 1/1
84 d infants incorrectly treated with ART after false-positive diagnosis (e.g., medication toxicities);
85 tion experiments confirm that XGSA can avoid false positive discoveries, while maintaining good stati
88 al shortcomings, including susceptibility to false positives due to artifactual peaks, poor localizat
89 e a matched total DNA input control to avoid false positives, effectively decreasing the sequencing c
90 ng, they also detect a problematic number of false positive EIC peaks and can also fail to detect rea
91 cific reasons why XCMS and MZmine 2 find the false positive EIC peaks that they do and in what ways t
93 (random sets of genes) to estimate power and false-positive error rate of methods applied to simulate
94 recently developed models which also include false positive errors (i.e. species detected in places w
97 ined with digital mammography (DM) decreases false-positive examinations and increases cancer detecti
103 ions] vs 60% [69 of 115 lesions]), and fewer false-positive findings than MR imaging (five vs 45) (P
105 % and 92.9%, respectively, for R1 (six fewer false-positive findings) and 92.3% and 96.4%, respective
108 For this analysis, ZIKAV IgM was considered false positive for samples interpreted as a DENV infecti
109 CA) on 91/99 specimens that were recorded as false positive (FP) or false negative (FN) compared to t
110 luded cancer detection rate (CDR), number of false-positive (FP) recalls, and incremental CDR for eac
111 ty, as indicated by the false-negative (FN), false-positive (FP), and fixation loss (FL) rates, on gl
113 rom 54% to 93%) in 10- to 12-year-olds and a false-positive fraction up to 35% in older subjects.
115 e often insufficient to completely eliminate false positives from environmental samples, which are es
118 .18-3.83) and had a predicted probability of false positive HCC greater than 10% regardless of larges
119 mL at transplant yielded a 50% lower risk of false-positive HCC (odds ratio [OR], 0.45; 95% confidenc
126 ed bioenergetic shunt that greatly minimizes false-positive hits, we identify mitoxantrone out of mor
130 the highest selectivities, yielding only one false positive; however, it was bias toward the most int
131 ely large fluorescence tags and the risk of 'false positive' identification when analyzing these rare
138 ovided from this bacterium in order to avoid false positives in the frame of the detection and the qu
142 e of the tested compounds may be measured as false positive inhibitors with the much-utilized ThT ass
143 ent years, most PPI networks still have many false positive interactions and false negative edge loss
149 hese spoilage species are liable to frequent false positives, long culture times and fungal contamina
150 n subjects with F0-F2 fibrosis, the rates of false-positive LSM results for F3-F4 fibrosis increased
154 hat the proposed method has low fractions of false positive/negative bouton detections (2/0 out of 18
158 t observed in convenience set samples and no false positive or negative identifications were observed
159 It can also be a rate-limiting step if high false positive or negative rates necessitate multiple ro
160 n of drugs in low concentrations and risk of false positive or negative results caused by mixed spect
164 biopsies, or other procedures performed for false-positive or indeterminate surveillance results.
165 with cirrhosis experience physical harm for false-positive or indeterminate surveillance tests-more
169 how differences between target compounds and false-positive peaks as high as 74%, as was the case for
170 We use this approach to show a reduction in false-positive peaks as well as improved consistency acr
171 Such analyses can produce a large number of false positive predictions, suggesting that sites suppor
175 ional 9 true positives being discovered at a false positive probability of 0.2 and 5 additional true
176 al design and analysis parameters can reduce false positives, provide greater resolution of species i
177 es of Crohn disease, showing how it controls false positives, provides power similar to that achieved
179 ined by means of next-generation sequencing (False Positive Rate (FPR), 3.5%; R5- or X4 tropic varian
181 accurate in QTN effect estimation, had less false positive rate and required less computing time tha
182 erogeneity; and an underestimation of actual false positive rate by Benjamini-Hochberg correction.
183 IsoMut, when tuned correctly, decreases the false positive rate compared to conventional tools in a
185 4-5 with a positive predictive value of 99%, false positive rate of 0.5%, and a sensitivity of 48%.
186 ghly malignant electroencephalography had an false positive rate of 1.5% with accuracy of 85.7% (95%
188 icted with sensitivities of 63% and 58% at a false positive rate of 6% and 7% at 12 and 24 hours, res
194 As a result, pKWmEB effectively controlled false positive rate, although a less stringent significa
195 ate of error discovery without affecting the false positive rate, particularly within the middle of r
200 suggested that pRSEM has a greatly decreased false-positive rate at the expense of a small increase i
209 redictive value to predict poor recovery (0% false-positive rate), and provided equal performance to
210 fractures at high sensitivity and with a low false-positive rate, as well as to calculate vertebral b
212 hip between various methods and compared the false positive rates and statistical power using both si
213 cy (for our benchmark, the true positive and false positive rates are 73% and 29%, respectively).
215 cator; although some variables have very low false positive rates for poor outcome, multimodal assess
223 the potential harms of treatment (ie, higher false-positive rates in low-prevalence populations) as s
224 on by history of coronary heart disease, the false-positive rates of association tests will be close
225 rue-positive rate ranging from 3% to 57% for false-positive rates ranging from 0.00001 to 0.001, resp
227 her USPSTF screening recommendations; harms (false-positive rates, false-negative rates, surgery rate
228 in low positive predictive values (PPVs) and false-positive rates, with a lack of precision in accura
229 Once the anti-HBc alone pattern is detected, false-positive reactivity should be ruled out and furthe
231 95%CI, 0.57-0.70), and a higher frequency of false-positive recommendations for peptide-receptor radi
232 of genomic copy number highlighted potential false-positive regions, thus emphasizing the importance
234 retention time prediction, text-mining based false positive removal/true positive ranking, chemical t
236 TBDRplus performed on positive cultures, the false-positive resistance rate for direct testing of MTB
241 ith different error properties; it minimizes false positives resulting from mapping errors and other
242 In either case, we found a high level of false positive results and a general lack of correlation
243 ing standard colorimetric assays often shows false positive results and has little correlation to the
244 sma samples that were HIV negative showed no false positive results in the detection of HIV-1 p24 ant
245 We here used proteomics to characterise false positive results occurring in the ERM as being due
246 edictive value of CMV PCR in saliva was 59%; false positive results were associated with lower viral
247 f 10 adenomas (90% sensitivity), without any false-positive results (100% positive predictive value).
249 ult in 15840 true-positive results and 15960 false-positive results (positive predictive value, 50%).
250 y 100%; 95% CI 88.4-100) with two additional false-positive results (specificity 99.9%; 99.7-100).
251 n additional 3 deaths, but yielded 1988 more false-positive results and 11 more overdiagnoses per 100
254 Commercial ELISA kits are known to give false-positive results for OTA concentrations when pheno
255 nt of genetic dependency, thereby leading to false-positive results in copy number-amplified regions.
256 hreshold of alpha = 2.5% for controlling for false-positive results or type 1 error, regardless of th
257 per into the tissue block, and occurrence of false-positive results using immunohistochemistry alone.
260 To explore reasons for false-negative and/or false-positive results, we used pfhrp2/3-specific PCR an
265 cers (IBCs) detected after a negative versus false-positive screening among women participating in th
266 91 of 1302) were detected among women with a false-positive screening as the most recent breast imagi
267 ing a negative screening as the reference, a false-positive screening examination increased the risk
269 th a negative (the reference group) versus a false-positive screening were estimated by using logisti
271 and 2.8 (95% CI: 1.8, 4.4) for women with a false-positive screening without and with needle biopsy,
278 tal herpes is associated with a high rate of false-positive test results and potential psychosocial h
279 varying amounts of CCDs sufficient to cause false-positive test results up to 2 kUA/L with nonglycos
283 ients, 150 (95% CI, 146-154) had one or more false-positive tests equating to a number needed to harm
284 nosed with infectious mononucleosis based on false-positive tests for primary Epstein-Barr virus infe
287 45/321 Xpert-positive retreatment cases were false-positive) than new cases (40/461) (14% [95% confid
288 tions and predicting arguably higher quality false positives that are located nearby the native bindi
289 ed by interference compounds, artifacts, and false positives that permeate the pool of initial hits.
291 ect over 90% of essential genes with minimal false positives using a compact 5 sgRNA/gene library.
293 o results) with LC-MS; on the other hand, 10 false positives were obtained elaborating data deriving
295 r missing data in one source, and can reduce false positives when multiple sources highlight the same
296 ng correction can generate a large number of false positives while multi-testing correction tremendou
298 sired false positive control to avoid excess false positives with the usage of an asymptotic chi-squa
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