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1 on VCF files using a new approach, called LB-Impute.
2 Missing covariates were imputed.
3 he proportions of undetected infections were imputed.
4 leukocyte antigen (HLA) serotypes were also imputed.
5 Missing data were imputed.
6 ion to treat, and missing data were multiply imputed.
7 In the GALA II study WBC types were imputed.
8 Missing covariate data were imputed.
9 GICS population); genotypes of two SNPs were imputed.
10 y, and SNPs that could not be genotyped were imputed.
11 age, and Karnofsky score, with missing data imputed.
12 st one dose of study drug, with missing data imputed.
13 puting genotype probabilities first and then imputing.
17 genetic model in an association analysis of imputed 2.5 million single-nucleotide polymorphism dosag
20 emely low sequencing coverage, by accurately imputing 5.7 million SNPs at a mean r(2) value of 0.98 i
24 ve US survey, we used multiple imputation to impute ABP-defined hypertension status for NHANES partic
30 included calculating the correlation between imputed and observed allelic dosage in a subset of sampl
33 nalysis pipeline can be applied to sequence, imputed, and genotyping array, e.g., "exome chip," data,
37 ata for patients with no resistance test was imputed based on the patient's risk of harboring drug-re
44 ts on isolated cell types, it is possible to impute cell proportions and adjust for them, but there i
45 s and 13,589 controls of European descent by imputing class I and II human leukocyte antigen (HLA) ge
46 (HLA) region was comprehensively studied by imputing classical alleles and polymorphic amino acid po
47 t random forest imputation may be useful for imputing complex epidemiologic data sets in which some p
51 and Medicaid Services, was used to calculate imputed costs for each primary treatment modality in a f
52 ing growth curve models, which enabled us to impute data at missing time points for each participant.
54 genome-wide significance in combination with imputed data from a GWAS in nsCPO triads (p = 2.73 x 10(
55 further discover new susceptibility loci, we imputed data from four GWAS of Asian non-smoking female
60 of the correlations was generally reduced in imputed data sets, and this effect increased with the am
61 additional whole-genome sequence and deeply imputed data sets, we report meta-analysis results for c
62 s such, we demonstrate filtering methods for imputed data that improve genotype concordance from 79.3
64 used multivariable regression with multiply imputed data to estimate associations while controlling
65 value or use all SNPs, handles genotyped and imputed data, can calculate and incorporate ancestry-inf
66 Based on the cartographies constructed from imputed data, we showed that the antigenic evolution of
69 ht-association threshold of P < 5E-06 in the imputed dataset were followed up in an independent sampl
70 r controlling for baseline utility and using imputed dataset, treatment was associated with a reducti
72 tic regression analyses on complete-case and imputed datasets to investigate sociodemographic and CSE
74 Finally, reanalysis of the European HapMap imputed Diabetes Genetics Replication and Meta-Analysis
76 cause and effect (i.e., left atrial dynamics impute disease events as consequences), disease classifi
78 novel computational method that allows us to impute drug response in very large clinical cancer genom
83 t by using GTEx data as a reference, one can impute expression levels in inaccessible tissues in non-
84 expression imputation and that incorporating imputed expression data can improve power to detect phen
88 ug repositioning by comparing transcriptomes imputed from GWAS data with drug-induced gene expression
94 ghting, and in models using cognitive scores imputed from the Telephone Interview for Cognitive Statu
96 arean rate data were available, the rate was imputed from total health expenditure per capita, fertil
97 These results highlight the utility of re-imputing from denser reference panels, until whole-genom
98 est for the joint effect of all measured and imputed functional variants which are associated with a
99 developed multi-tissue imputation methods to impute gene expression in uncollected or inaccessible ti
101 individual's genetic profile and correlates 'imputed' gene expression with the phenotype under invest
102 The procedures these technologies use to impute genetic data, therefore, greatly affect downstrea
108 p imputation, and lastly how the clusters of imputed genotype are pieced together as the final imputa
109 We applied variance-component methods to imputed genotype data for 11 common diseases to partitio
112 f bone using a combination of WGS and deeply imputed genotype data, we have identified five novel gen
117 SNPs using the 'iCOGS' genotyping array and impute genotypes for a further 1,284 using 1000 Genomes
118 the combined reference panel increased well-imputed genotypes (with imputation quality score >/=0.4)
119 FEV1/FVC with 1000 Genomes Project (phase 1)-imputed genotypes and followed up top associations in 54
122 e large scale genome-wide data, allowing for imputed genotypes by modelling time to event outcomes un
124 ved genotypes for sequenced subjects and the imputed genotypes for nonsequenced subjects is unbiased.
125 We then examined the entire data set using imputed genotypes from 1917 cases and 3858 control indiv
128 ation analysis in the discovery cohort using imputed genotypes of the major histocompatibility comple
130 tudy we investigated the impact of employing imputed genotypes when using more elaborated models of p
131 rd progression from low-coverage sequence to imputed genotypes, overcoming barriers that at present r
137 es and 9,979 controls of European ancestry), imputing genotypes utilising the 1000 Genomes Project.
139 g the Revised NEO Personality Inventory, and imputed GTF2I rs13227433 from saliva-derived DNA using c
140 hen meta-analysed with those from two deeply imputed GWAS replication cohorts (n = 1610 and 13 749).
141 h excessive missing data, and approaches for imputing highly skewed continuous distributions that are
147 Using a validated prediction algorithm, we imputed HLA-C cell surface levels in 228 individuals fro
149 an and median observed and missing at random-imputed HRQOL scores were calculated, followed by sensit
150 of asparaginase-induced immune responses, we imputed human leukocyte antigen (HLA) alleles in patient
151 ough a genome-wide association study (GWAS), imputed human leukocyte antigen (HLA) alleles, exome arr
154 r each selected SNP those untyped SNPs to be imputed in the add-one two-step imputation, and lastly h
156 ome sequencing (WGS) of 8,453 Icelanders and imputed into 1,840 cases and 129,016 control women, foll
157 le-genome sequencing of 2,636 Icelanders and imputed into 4,572 BCC patients and 266,358 controls.
158 ome sequencing of 2,636 Icelanders that were imputed into 5,419 kidney stone cases, including 2,172 c
159 were estimated with data for training costs imputed into a regression analysis with health-care expe
160 6 Icelanders and found variants that we then imputed into the genomes of approximately 398,000 Icelan
161 al observed in European subjects was for the imputed intronic SNP rs1830298 in ALS2CR12 (telomeric to
162 thium-responsive patients with controls, two imputed markers attained genome-wide significant associa
163 performed on the genotyped and 1000 Genomes-imputed markers separately for each study, and combined
164 INTERMACS profile 1 alone, missing at random-imputed mean and median HRQOL scores were similar to obs
165 nd 3 months after implantation, whereas MNAR-imputed mean scores were lower (>/=5 points) at baseline
169 AR contains procedures to filter, normalize, impute missing value, aggregate peptide intensities, per
170 pproaches of using regularized regression to impute missing values of high-dimensional data that can
171 d at least one post-baseline assessment, and imputed missing data with the last observation carried f
177 teractions among bZIP transcription factors, imputing missing present-day interactions among the bZIP
178 Such pseudo-array staircases are able to impute more accurately than the classic one-step imputat
179 l as from other omics, and 2) simultaneously impute multiple missing omics datasets by an iterative a
181 e-nucleotide polymorphisms (SNPs) (including imputed ones) fall into non-coding regions, making it di
182 4022 SNPs and 263,531 sequence variants were imputed onto the population using 9K iSelect SNP genotyp
183 (Stage 1) or approximately 200 000 (Stage 2) imputed or genotyped single variants and BMI, and summar
185 completion (LRMC) model is similar to Mendel-Impute, our matrix co-clustering factorization (MCCF) mo
187 ity analysis, in which missing data were not imputed, peak VO2 at 24 weeks decreased by -0.63+/-0.375
188 on HR: 0.92; 95% CI: 0.84 to 1.01; p = 0.10; imputed population HR: 0.97; 95% CI: 0.92 to 1.03; p = 0
189 dence interval [CI]: 0.71 to 1.06; p = 0.16; imputed population HR: 0.99; 95% CI: 0.89 to 1.09; p = 0
190 on HR: 0.92; 95% CI: 0.79 to 1.07; p = 0.26; imputed population HR: 0.99; 95% CI: 0.92 to 1.06; p = 0
191 ifferences in survival between the naive and imputed populations at 30 days (naive population hazard
192 or patients with unknown race, we multiplied imputed race to calculate age-, race-, and serotype-spec
193 s, looking at studies that have been able to impute rare variants, methods behind merging reference p
194 and potential of larger reference panels to impute rare variants, while recognizing that increasing
196 ind merging reference panels, approaches for imputing rare variants, and methods for analyzing rare v
197 ew the additional challenges that arise when imputing rare variants, looking at studies that have bee
198 ciation with rs1830298 was replicated in the imputed results from the combined GWAS (P = 3 x 10(-6)),
199 15), effect -1.24 years of maternal life per imputed risk allele in parent; sex difference, P=0.011),
200 o a limited sample size, we further analyzed imputed rs2735383 genotypes (r(2) > 0.999) of 47,640 bre
202 es for milk production and curly coat, using imputed sequence variants, and identified variants assoc
205 an in a prior national civilian survey (with imputed/simulated age at enlistment), whereas post-enlis
206 osome 20q11 [P= 1.72 x 10(-8) for rs3746446; imputed Single Nucleotide Polymorphism (SNP) rs6088703 P
207 ects and more than 7.8 million genotyped and imputed single nucleotide polymorphisms (SNPs) were anal
208 I and approximately 2.5 million genotyped or imputed single nucleotide polymorphisms among 86 757 ind
210 ted for association with 27.7 M genotyped or imputed single-nucleotide polymorphisms separately in th
214 co fine-mapping approach using genotyped and imputed SNP data for 6,608 endometrial cancer cases and
216 8), RBBP8 (OR 0.76; 95% CI 0.62-0.94) and an imputed SNP near CDKN2B-AS1 (OR 0.79; 95% CI 0.64-0.98)
217 oid the genotype imputation step by directly imputing SNP statistics, e.g. Directly Imputing summary
219 puted to 1000 Genomes Project data, and well-imputed SNPs (>0.01 minor allele frequency) were analyse
220 ed an average of 79% (SE = 8%) of hg(2) from imputed SNPs (5.1x enrichment; p = 3.7 x 10(-17)) and 38
221 es (DHSs) from 217 cell types spanned 16% of imputed SNPs (and 24% of genotyped SNPs) but explained a
222 an additive genetic model, revealed several imputed SNPs (eg, rs115231074: odds ratio [OR], 1.22 [P
224 ciation between 1000 Genomes Project (1000G) imputed SNPs and electrocardiographically measured QT we
226 erage and to interrogate additional SNPs, we imputed SNPs from the 1000 Genomes Project reference pan
228 with approximately 2.5 million genotyped and imputed SNPs in 9,055 participants of European descent a
230 e strongest associations uncovered were with imputed SNPs residing within the FGFR2 (rs1219515, P = 1
231 summary, family-based GWAS meta-analysis of imputed SNPs revealed novel genomic variants in (or near
232 explained (PVE) for DMA% by all measured and imputed SNPs was 16% (p = 0.08), which was reduced to 5%
233 after quality exclusions, 501 typed and 1232 imputed SNPs were included in logistic regression models
235 rce-specific health associations from the 10 imputed source contribution time series were combined, r
237 es of four lipid traits, we publicly release imputed summary statistics at 1000G SNPs, which could no
238 ectly imputing SNP statistics, e.g. Directly Imputing summary STatistics (DIST) proposed by our group
240 rage (0.15x) sequencing with a new method to impute the ancestral haplotype space in 1,887 commercial
242 rior to and following PCV use can be used to impute the indirect protection afforded by PCV in unvacc
243 representation of the fluxes and ability to impute the missing data in between the measurements.
244 ge of these additional related phenotypes to impute the phenotype of interest or target phenotype and
246 ich uses only GWAS summary statistics to (i) impute the summary statistics at unmeasured eQTLs and (i
247 EGMIX uses this accurate LD estimates to (i) impute the summary statistics at unmeasured functional v
249 two-step imputation may improve accuracy by imputing the low density genotyped study animals to a me
250 KNN-TN generally has improved performance in imputing the missing values of the different datasets co
257 based on millions of samples with array data imputed to a large fully sequenced reference panel and o
259 alytic activity and/or selectivity have been imputed to non-covalent interaction between the reaction
260 e Illumina HumanCoreExome array and variants imputed to the 1000 Genomes Project and UK10K haplotypes
261 nome-wide association analysis of 34 studies imputed to the 1000 Genomes Project reference panel and
267 mpirically evaluate imputation accuracy when imputing to a 1000 Genomes Phase 3 versus a Phase 1 refe
272 provides a flexible and transparent means to impute univariate missing data under general missing-not
273 uses a relevant reference panel to directly impute unmeasured SNP statistics based only on statistic
274 risk loci, training risk prediction models, imputing untyped variants and fine-mapping causal varian
275 he Infinium Omni Express bead microarray and imputed up to reference panels from the 1000 Genomes Pro
276 SNPs (minor allele frequency>0.05) that were imputed using 1000 Genomes Phase 1 European data (R(2)>0
277 enotypes for six million common variants are imputed using 1000 Genomes Project and UK10K as the refe
278 ysis of six genome-wide association studies, imputed using a merged reference panel of 1,000 Genomes
280 an 5,000,000 SNPs were directly genotyped or imputed using the 1000 Genomes Project reference panels.
281 ymorphism panel of soybean with missing data imputed using various methods, (2) evaluate the imputati
284 association between 8,114,394 genotyped and imputed variants across the genome and risk for developi
285 We tested for association between these imputed variants and non-HDL cholesterol levels in 119,1
286 ndividuals that all approximately 17 million imputed variants explain 56% (standard error (s.e.) = 2.
288 ion and meta-analysis on close to 15 million imputed variants from three large collections of AD fami
290 fying by ancestry, we analysed genotyped and imputed variants in Melanesians (607 cases and 1,229 con
291 lly more powerful than the use of accurately imputed variants only and the use of sequencing data alo
293 s (NHLBI) Exome Sequencing Project (ESP), we imputed whole-exome sequence data into 13 719 African Am
294 with SNP imputation, common HLA alleles were imputed with greater accuracy than low-frequency variant
298 llumina Human 660WQuadv1C BeadChip array and imputed with the Markov Chain Haplotyping algorithm usin
299 on of some individuals is based on genotypes imputed with the same accuracy as our Yorkshire populati
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