ライフサイエンスコーパス: COD

1 standardized extraction tool, compiled, and coded.

2 re audio-recorded, transcribed verbatim, and coded.

3 by representing them with overlapping neural codes.

4 lassification of Disease-9th edition (ICD-9) codes.

5 ation of Diseases, Ninth and Tenth Editions, codes.

6 acterial peritonitis identified by ICD-9/CPT codes.

7 esponse element in pattern-based information codes.

8 ational Classification of Diseases diagnosis codes.

9 al Classification of Diseases, 10th revision codes.

10 providing a reference for spike timing-based codes.

11 terviews, and hospital and death certificate codes.

12 on and its rather distant cousin, predictive coding.

13 ll, and therefore may not affect information coding.

14 cal layers, and rhythms implement predictive coding.

15 n induced a switch from absolute to relative coding.

16 eading frames from being regarded as protein-coding.

17 d thematically using deductive and inductive coding.

18 nt subset of neurons than experiential value coding.

19 eases, Ninth Revision, Clinical Modification codes 115.00-115.99) during 2012-2014.

20 atalyst with free bidentate phosphines is Ni(cod)(2), which accounts for ~50% of the reports surveyed

21 alues for influent TSS (61-820 mg L(-1)) and COD (384-1505 mg L(-1)), demonstrating a robust system f

22 specifically interneuronal, affiliations and coded a network of proteins comprising a few highly inte

23 Both Poisson frameworks preserve the coding accuracy and robustness to neuron loss of the ori

24 DNA is a threat to the genomic integrity and coding accuracy of the chromosomes of all living organis

25 t functional specializations of the Atlantic cod Ahr's.

26 ant association for walleye pollock, and (d) cod and pollock will likely have reduced recruitment giv

27 rs are statistically significant for Pacific cod and walleye pollock recruitment, (c) separately anal

28 Others can integrate the codes and implement the method in academic software.

29 the implications of our findings for neural coding and for brain-controlled bionic hands.

30 ogical processes had variable proportions of coding and non-coding mutations, with chromatin remodeli

31 ys, including Wnt and Notch, altered by both coding and non-coding mutations.

32 y deliver more meaningful prediction in both coding and non-coding regions of the cancer genome.

33 For somatic point mutations in coding and non-coding regions of the genome, we propose

34 ed for processing and/or degradation of both coding and non-coding RNAs.

35 MRX restricts transcription of coding and noncoding DNA by a mechanism that does not re

36 NA, while conversely most studies of protein-coding and noncoding genes frequently ignore any intron-

37 res from neutrality across the locus in both coding and noncoding regions.

38 ly recruits the Set3 complex to both protein-coding and noncoding RNA (ncRNA) genes via a SUMO-intera

39 refore enables cells to selectively regulate coding and noncoding RNAs.

40 late the stability and, hence, expression of coding and noncoding RNAs.

41 provides a blueprint for dissection of their coding and noncoding roles.

42 We designed a 20.5 Mb array targeting coding and regulatory regions of genes with a known role

43 In particular, using Freedom House's coding and terminological classifications, the proportio

44 sting a role for cross-frequency coupling in coding and transmitting retrieved spatial information.SI

45 result from difficulties related to landmark coding, and predict recovery of allocentric strategies i

46 tional Classification of Diseases diagnostic codes are used to estimate acute gastroenteritis (AGE) d

47 ficiaries were more likely to have surgeries coded as complex (15.6% of cases vs 8.8%, P < .0001), an

48 andom forests using diagnostic and procedure codes as well as sociodemographic features were used to

49 g approach derived from principles of neural coding as a framework to understand working memory limit

50 :DNA hybrids and RNAPII are detected at gene-coding as well as at intergenic areas when double-strand

51 ticularly, the knowledge learnt from protein-coding ASD risk genes was transferred to the prediction

52 ife Identification Numbers (LINs), which are codes assigned to individual genomes based on reciprocal

53 ptured in UHDDS); 406 (86.0%) were correctly coded based on chart review.

54 read divergence remains a major issue for MC codes based on acceptance-rejection sampling.

55 Then, signals are reformatted to reduce the coding biases inherent in peripheral mechanics, and wind

56 HGNC) guidelines for naming not only protein-coding but also RNA genes and pseudogenes, and outline t

57 rial transcriptomic data commonly ignore non-coding but functional elements e.g. small RNAs, long ant

58 Disruption of this stem abolishes the non-coding, but not the coding, function of the endogenous x

59 [Z = A or G]), glycine (coded by GGX), Ser (coded by AGY), and Arg (coded by CGX and AGZ).

60 (coded by GGX), Ser (coded by AGY), and Arg (coded by CGX and AGZ).

61 ty, including cut-like homeobox 2 (a protein coded by CUX2), Glu504Lys of acetaldehyde dehydrogenase

62 G]), alanine (coded by GCX), aspartic acid (coded by GAY [Y = U or C]), glutamic acid (coded by GAZ

63 (coded by GAY [Y = U or C]), glutamic acid (coded by GAZ [Z = A or G]), glycine (coded by GGX), Ser

64 (coded by GUX [X = U, C, A or G]), alanine (coded by GCX), aspartic acid (coded by GAY [Y = U or C])

65 c acid (coded by GAZ [Z = A or G]), glycine (coded by GGX), Ser (coded by AGY), and Arg (coded by CGX

66 e only seven primordial amino acids: Valine (coded by GUX [X = U, C, A or G]), alanine (coded by GCX)

67 as methylation can modulate the information coded by the sequence, process named epigenetics.

68 creasingly stable in time as the information coded by those patterns transitioned from low-to-high le

69 decreased correlations increased information coding capacity.

70 ge N = 320K), conditioning on a broad set of coding, conserved and regulatory annotations.

71 regions formed abstract representations that coded cross-triad relationships with a common geometric

72 l cortex: the Allen Brain Observatory Visual Coding dataset.

73 Models incorporating coded diagnoses and procedures yielded a mean area under

74 omic regions or de novo, from previously non-coding DNA.

75 performed to determine the contributions of coding DNMs to an individual's OFC risk.

76 least as high as that observed for damaging coding DNVs.

77 Dementia was identified from diagnosis codes documented in a beneficiary's first 3 years of obs

78 Due to its apparent stability, use of Ni(COD)(DQ) as a precatalyst allows reactions to be conveni

79 Recent advances in optical coding, drug delivery, diagnostics, tissue engineering,

80 uction hypothesis, a theory of retinal color coding emerged in which the three most common retinal ga

81 ncounter between 2008 and 2018 who moved zip codes exactly once or never moved.

82 By providing coded examples using integrated nested Laplace approxima

83 llelic deletions were predicted to result in coding exon disruption.

84 greater identity across species than nearby coding exons, but their physiological role and molecular

85 Two ophthalmologists without coding experience used an interactive application in MAT

86 In predictive coding, experience generates predictions that attenuate

87 t is unknown whether correlated noise limits coding fidelity.

88 ng frames predicted from the genomic islands coded for enzymes belonging to the Nitro-FMN-reductase s

89 nriched for innate immune-related functions, coded for nonrandom protein-protein interaction networks

90 These findings are notable because SLC7A11 codes for a cysteine-glutamate anti-porter regulating le

91 le neurons can generate complementary neural codes for acoustic stimuli.

92 nefit RMNCH was determined using CRS purpose codes for all donors except Gavi, the Vaccine Alliance;

93 ression to PV(+) interneurons: Cox6a2, which codes for an isoform of a cytochrome c oxidase subunit.

94 tion of Disease for Oncology, Third Edition, codes for both morphologic features (melanoma, 8720-8790

95 proximately 350 kb downstream of GDF6, which codes for growth and differentiation factor 6.

96 ification of Diseases, 9thRevision diagnosis codes for infective endocarditis (IE) in the National In

97 PYGM codes for myophosphorylase, the enzyme catalyzing the in

98 nce imaging (fMRI) to investigate the neural codes for representing stimulus information held in diff

99 ed presence of a microbiology order, billing codes for surgical site infections and post-procedural a

100 hine learning, CEFCIG reveals unique histone codes for transcriptional regulation of reported CIGs, a

101 y linked to one of the ICD-9-CM or ICD-10-CM codes for vitreous opacities were identified.

102 to have missense mutations in VPS4A, a gene coding for an ATPase that regulates the ESCRT-III machin

103 GRM3 (the gene coding for mGluR3) is also genome-wide associated with r

104 RNAs coding for nAChR monomeric subunits and/or concatamers w

105 Compared to FF, FFPE transcripts coding for nuclear/cytoplasmic proteins involved in DNA

106 ms in the CHRNA5-CHRNA3-CHRNB4 gene cluster, coding for the alpha5, alpha3, and beta4 nicotinic acety

107 e show that an OCS pipeline focused on genes coding for transcription factors increases isoform detec

108 Here, we develop an efficient coding framework for higher-level cognitive processes in

109 Within a predictive coding framework sensory information could be down-weigh

110 Crashes were coded from the video and other data streams by trained a

111 nt loci across 19,155 disease classification codes from 320,644 participants in the UK Biobank, repre

112 ing International Classification of Diseases codes from May 20, 2014, through October 22, 2019: 362.7

113 hrough Systematized Nomenclature of Medicine codes from the ESPRESSO (Epidemiology Strengthened by hi

114 nearly indistinguishable by other diagnostic codes from those whose admissions will not have a sepsis

115 s stem abolishes the non-coding, but not the coding, function of the endogenous xbp-1 transcript.

116 inversions associated with expressed protein-coding fusions, breakend hypermutation, and acral, but n

117 Atlantic cod (Gadus morhua) has recently emerged as a model organ

118 cient translational bypassing of a 50-nt non-coding gap in a phage T4 topoisomerase subunit gene (gp6

119 luenced by a single QTL encompassing the Adh-coding gene and its known regulatory locus, delta-1.

120 sly undescribed mechanism of de novo protein-coding gene evolution.

121 verlap was found in plastid-targeted protein-coding gene families compared with Arabidopsis, but an a

122 The postsynaptic adapter protein-coding gene, SHANK2, located on Chromosome 11q13, was di

123 50.37-50.58 Mb, mm10) containing two protein-coding genes (Hnrnph1, Rufy1) that was necessary for red

124 stream genes in mouse, including 117 protein-coding genes and 144 lincRNA genes, 93.7% of which are m

125 We identify 1434 protein-coding genes and 39,806 noncoding regions for which mole

126 ndings implicate more than 5% of all protein-coding genes and provide evidence for gene sets involved

127 Genetic variants that inactivate protein-coding genes are a powerful source of information about

128 SSP-coding genes are frequently overlooked, because genome a

129 show that homologs of the identified protein-coding genes as well as genes in close proximity to the

130 response to P starvation, 40% of all protein-coding genes exhibit a transition from one chromatin sta

131 sis that gene expression profiles of protein-coding genes expressed in peripheral white blood cells (

132 Forty of the protein-coding genes in GRCh38 are missing from Ash1; however, a

133 we used new pol II promoters from endogenous coding genes to express crRNA for Cas12a and obtained a

134 istinct proteins covering 95% of Mtb protein-coding genes using artificial antigen-presenting cells (

135 Of the 23,248 predicted protein-coding genes, 12,346 venom-gland-expressed genes constit

136 o 24 chromosomes and annotate 32,690 protein-coding genes.

137 accessions as the outcome of SNPs in enzyme-coding genes.

138 CBC in the nucleus, with a focus on protein-coding genes.

139 INFERence of the molecular mechanisms of NOn-coding genetic variants (SparkINFERNO), a scalable bioin

140 fy novel therapeutic targets in the vast non-coding genome to enhance radiation therapy.

141 e bioinformatics pipeline characterizing non-coding genome-wide association study (GWAS) association

142 pe of infrequent driver mutations in the non-coding genome.

143 Chirality codes, global, multivariate descriptors, are then introd

144 patient code or >=2 outpatient CHD diagnosis codes >30 days apart documented outside of pregnancy and

145 Of 18 048 ARFI-coded hospitalizations, 1064 (6%) included RT-PCR testin

146 -productive splicing events in 7,757 protein-coding human genes, of which 1,246 are disease-associate

147 According to the efficient coding hypothesis, sensory systems are adapted to maximi

148 cluded adults aged 18-90 years with COVID-19 coded in their electronic medical records between Januar

149 effect of correlated activity on population codes in macroscopic fMRI data.

150 oding analyses suggested observational value coding in amygdala neurons occurred in a different subse

151 tions for using XDream to investigate neural coding in biological preparations.

152 mon neurophysiological substrate for spatial coding in navigation and episodic recall.

153 he order of 10(-3)), they affect information coding in populations on the order of 100 s of neurons.

154 smitter systems in modulating working memory coding in prefrontal circuits.SIGNIFICANCE STATEMENT Ong

155 ibition of MEC led to a disruption of border coding in RSC, but not vice versa, indicating allocentri

156 We examined preparatory coding in the human hippocampus and mPFC, two regions th

157 arthritis were labeled as IDRIs if discharge codes included opioid and/or amphetamine misuse.

158 Non-coding IPS1 RNA is highly expressed during Pi starvation

159 motion-related VIP neuron activity to visual coding is not known.

160 VINR, a Drosophila VSR-interacting long non-coding (lnc) RNA that activates non-canonical innate imm

161 ses and the detection of novel expressed non-coding loci.

162 ebellar activity through inhibition via rate coding mechanisms.

163 edical record abstractions and available ICD codes (median age, 69 years [interquartile range, 54 to

164 Switching between these two spatial coding modes was supported by the interaction between ex

165 microRNAs (miRs) are small non-coding molecules that regulate post-transcriptional targ

166 genes and mechanisms that are altered by non-coding mutations and offer insights into additional canc

167 r gene expression signatures as samples with coding mutations in these genes.

168 RNA splicing is primarily altered by non-coding mutations in this cohort, and samples containing

169 s in this cohort, and samples containing non-coding mutations in well-known RNA splicing factors exhi

170 ilitate the identification of functional non-coding mutations, we present dbInDel, a database where w

171 proliferation pathways altered primarily by coding mutations, while developmental pathways, includin

172 s had variable proportions of coding and non-coding mutations, with chromatin remodeling and prolifer

173 nt and Notch, altered by both coding and non-coding mutations.

174 n the DNA that modulates the position of the coding nucleotide and thereby impacts the identity of th

175 racterized by the transcription factor motif codes of their promoters.

176 Here, we hypothesize that the coding of foreseeable outcomes is potentially unclear fr

177 ed light on the transformation of rate-place coding of resolved harmonics along the auditory pathway.

178 ed sensory receptors able to provide dynamic coding of sound signals.

179 Adaptive coding of stimuli is well documented in perception, wher

180 ined neuron populations for grouped-ensemble coding of survival behaviors.

181 urs, calculation of CT FFR values, and color coding of the coronary tree according to CT FFR.

182 females have anomalies in their gene arrays coded on the X chromosome that result in significantly d

183 identification relies on diagnosis/procedure codes or lists of patients diagnosed or treated by speci

184 fication of Diseases, Ninth Revision (ICD-9) codes or their Tenth Revision equivalent were used to de

185 high-resolution surface features, with phase coding organized to support this function.

186 hat most associated variants fall in the non-coding part of the human genome.

187 for both the identification of candidate non-coding pathogenic variants and their functional validati

188 he core autophagy gene Atg16L1 and its T300A coding polymorphism identified by genome-wide associatio

189 t, when a purine nucleotide was in the first coding position, DNA synthesis fidelity was similar to t

190 d messenger RNAs) and others lacking protein-coding potential, named noncoding RNAs.

191 uld generate chimeric human-viral mRNAs with coding potential.

192 However, diagnosis and coding practices vary widely between hospitals and are c

193 n grid spacing, no difference in the spatial coding properties of the grid cells across all three gro

194 thin these three groups have similar spatial coding properties.

195 and protein, the ribosome translates mRNA to coded protein in all living systems.

196 Temporal coding quality was evaluated as vector strength in respo

197 ct introgression of a small part of the BCO2 coding region (<3 kb) in S. discolor and S. vitellina, i

198 s process requires that the ASOs bind in the coding region and reduce the target mRNA by RNase H1 whi

199 strongly suggest a single-base change at the coding region of ClVST1(97) as a major molecular event d

200 which is an expansion of CAG repeats in the coding region of the causative genes that are otherwise

201 -associated risk loci are located in the non-coding region of the genome and therefore, their target

202 lso increase RNA Polymerase I loading to the coding region of the rDNA and this is Ncl dependent.

203 our MGW-prioritization approach to three non-coding regions associated with systemic lupus erythemato

204 ific HLA peptides derived from annotated non-coding regions could elicit anti-tumor immune responses.

205 mutations in pbp1, pbp2, and/or pbp3 within coding regions near known amoxicillin binding motifs.

206 tructure, expression, or function of protein-coding regions of cancer-biology related genes (gHFI) de

207 tion of VACV transcripts start or end within coding regions of neighbouring genes.

208 Recent genomic analyses revealed that the coding regions of PbANKA and the closely related Plasmod

209 ults uncover a function for ribosomes on non-coding regions of RNAs and reveal the mechanisms underly

210 meaningful prediction in both coding and non-coding regions of the cancer genome.

211 An analysis of the coding regions of the genome in 886 index cases of PID f

212 derstanding of the rules that govern the non-coding regions of the genome is less complete than our u

213 or somatic point mutations in coding and non-coding regions of the genome, we propose CScape-somatic,

214 less complete than our understanding of the coding regions.

215 ive under-characterization of 90% of protein coding regions.

216 affected transcripts but rather the protein-coding regions.

217 most of the sites were located within genes' coding regions.

218 ecular inversion probes that targeted mainly coding regions.

219 eed to understand the functional role of non-coding regulatory elements (REs).

220 ticated simulations to be set up with little coding required, thus lowering entry barriers to new use

221 Metabolism Regulator (lincNMR) is a long non-coding RNA (lncRNA) which is induced in hepatocellular c

222 re sites for RNA biology including small non-coding RNA (ncRNA) mediated gene silencing.

223 PPARalpha directly upregulates the long non-coding RNA gene Gm15441 through PPARalpha binding sites

224 The long non-coding RNA NEAT1 serves as a scaffold for the assembly o

225 Long intergenic non-coding RNA-Nucleotide Metabolism Regulator (lincNMR) is

226 (2.94-fold), GWAS loci (1.52-fold), and non-coding RNAs (1.44-fold), compared with random distributi

227 Long non-coding RNAs (lncRNAs) are defined as non-protein-coding

228 Long non-coding RNAs (lncRNAs) are important regulators of develo

229 Long non-coding RNAs (lncRNAs) are often aberrantly expressed in

230 Non-coding RNAs are fundamental to the competing endogenous

231 Circular RNAs (circRNAs), a class of non-coding RNAs generated from non-canonical back-splicing e

232 We find that alignments for several long non-coding RNAs previously shown to lack covariation support

233 of EVs identifies diverse RBPs and small non-coding RNAs requiring the LC3-conjugation machinery for

234 MicroRNAs (miRNAs) are small non-coding RNAs that have been successfully identified to be

235 Small RNAs are non-coding RNAs that play important roles in the lives of bo

236 MicroRNA-27a/b are small non-coding RNAs which are reported to regulate inflammatory

237 t eukaryotic pre-messenger RNAs and long non-coding RNAs, introns are removed through the process of

238 Enhancer RNAs (eRNA) are unstable non-coding RNAs, transcribed bidirectionally from active reg

239 ons, and regulation of transcription via non-coding RNAs.

240 ng and/or degradation of both coding and non-coding RNAs.

241 nonlinear mixed selectivity may be a general coding scheme exploited by the brain for reliable and ef

242 A stable coding scheme simplifies readout for WM-guided behaviour

243 results indicate that the brain regions and coding schemes supporting relations and movements betwee

244 ds as well as an enhancement of the neurons' coding selectivity.

245 techniques that are needed to interpret the coded sensor outputs.

246 t interact in three dimensional space, while coding sequence duplicates are rare, GC-rich, short, and

247 trains have over an order of magnitude fewer coding sequence mutations outside of duplicated domains

248 We then use genome editing to disrupt the coding sequence of a S. rosetta C-type lectin gene, rose

249 The binding site within the beginning of the coding sequence of the prfA gene, which encodes the mast

250 P mutations are, however, relatively rare in coding sequence, in part because RIP preferentially atta

251 AAV-PHP.B vector carrying the mouse Slc25a46 coding sequence.

252 R) and rare codons at the beginning of their coding sequence.

253 icrobial community by cataloging the protein-coding sequences (CDS) present in the metagenome of the

254 931,698 reads were annotated into 11,676 coding sequences (CDS), which were manually curated into

255 ary transcripts of eukaryotic nuclear genes, coding sequences are often interrupted by U2-type intron

256 ll-known mutagen, has been maintained within coding sequences of crucial plant and animal genes.

257 atial orientation of regular repeats of rDNA coding sequences within the nucleoli.

258 rnative reading frames, we found a conserved coding signature in an alternative frame in exons 2 and

259 ), a web-based interface where users with no coding skills can compute the generation and post-select

260 These data indicate that non-coding somatic mutations disrupt the PAX8 transcriptiona

261 other hand, allows for identification of non-coding somatic variation and expanded estimation of back

262 1 snRNP (U1), vertebrates' most abundant non-coding (spliceosomal) small nuclear RNA, silences proxim

263 ies during new learning leads to dissociable coding strategies in hippocampal subfields, in line with

264 These differential coding strategies may favor temporal precision of cerebe

265 al Classification of Diseases, 10th Edition, coding strategies.

266 me information along with an ensemble pMHC-I coding strategy, and developed a group feature selection

267 ed whether the same brain regions and neural codes supporting spatial navigation are recruited when h

268 We identified clustering of non-coding SVs around neuroactive ligand-receptor interactio

269 al Classification of Diseases, 10th Edition, coding systems, evaluating estimates of two previously p

270 rts of an HIV algorithm from Medicaid claims codes that have been compared with an HIV surveillance s

271 For specific codes, the overall PPV, NPV, sensitivity, and specificit

272 ive debriefs between coach/coachee pairs, co-coding themes based on established principles of effecti

273 input areas, possibly differing in terms of coding, timing, and direction of information flow (e.g.,

274 3, employing diagnoses, drugs, and procedure codes to define diseases and procedures.

275 nmeasured confounders and the use of billing codes to identify cohorts.

276 ulation of reported CIGs, and utilizes these codes to predict CIGs and their master regulators with h

277 eins at DNA damage sites serve as DNA damage codes to recruit specific DNA repair factors.

278 ter streams with low chemical oxygen demand (COD) to nitrogen (C/N) ratios.

279 that lncRNAs are distinct from both protein-coding transcripts and genomic background noise in terms

280 ng RNAs (lncRNAs) are defined as non-protein-coding transcripts that are at least 200 nucleotides lon

281 reviously unreported subset of small peptide-coding transcripts was identified from these lncRNA loci

282 ate the probing of the spatiotemporal neural codes underlying behaviour.

283 coding was stimulus specific, as opposed to coding value independent of the identity of the option.

284 e population sequencing data in studying non-coding variant classes.

285 The strongest coding variant in schizophrenia GWAS is a missense mutat

286 Rare and low-frequency functional protein-coding variants (minor allele frequency, <=5%) measured

287 tients with nsCL/P and identified three rare coding variants (p.Ala86Thr, p.Met91Iso and p.Arg546Gln)

288 e regulatory role of enhancer-associated non-coding variants in cancer epigenome, and to facilitate t

289 Coding variants in TMEM175 are likely to be responsible

290 Previous genome-wide scans found many non-coding variants under selection, suggesting a pressing n

291 noncoding variants and/or by rare but severe coding variants, many de novo.

292 ast genetic diversity as naturally occurring coding variants, yet the impact of these variants on pro

293 needed to identify individual risk genes, as coding variation across many genes confers risk for SCZ

294 0 weeks after transplantation; adverse event coding was centralised.

295 We also found that OFC value coding was stimulus specific, as opposed to coding value

296 tely insured, and patients in low-income ZIP codes were less likely than those in higher income areas

297 Diagnostic criteria and procedure codes were used to identify condition at admission, incl

298 tivity was greater for persons living in zip codes with lower annual household income.

299 ntegrating the concepts of neural population coding with distributed processing.

300 Results are color-coded, with emphasis on buried groups.