ライフサイエンスコーパス: single nucleotide polymorphism

1 for monitoring local structural changes and single nucleotide polymorphism.

2 core for BMI (PRSBMI) using almost 1 million single nucleotide polymorphisms.

3 nt (P < 5 x 10(-8)) loci with 68 independent single nucleotide polymorphisms.

4 Each trait was associated with different single nucleotide polymorphisms.

5 ly determined basing on microbiome data than single nucleotide polymorphisms.

6 del included a polygenic risk score with 313 single nucleotide polymorphisms.

7 t summarizes genetic information from 86 613 single-nucleotide polymorphisms.

8 graphy measures between 116 ROIs and 565 373 single-nucleotide polymorphisms.

9 = 11,263-331,679) and genome-wide autosomal single-nucleotide polymorphisms.

10 enhancers show stronger depletion of archaic single-nucleotide polymorphisms.

11 d, which contains ~15.7 million high-quality single-nucleotide polymorphisms.

12 genome and detection of pairwise core genome single-nucleotide polymorphisms.

13 ide association studies using 1000-G imputed single-nucleotide polymorphisms.

14 (3) a summary genetic risk score based on 49 single nucleotide polymorphisms, (4) smoking, (5) diet q

15 However, higher 52-single nucleotide polymorphism AMD genetic risk score wa

16 sauce isolates by whole-genome high-quality single-nucleotide polymorphism analysis.

17 of crop species typically carry millions of single nucleotide polymorphisms and many copy number and

18 Nine single nucleotide polymorphisms and seven indels disting

19 l human isolates shared closely related core single-nucleotide polymorphisms and blaNDM genetic conte

20 In total, we analyzed 8,582,968 single-nucleotide polymorphisms and conducted a meta-ana

21 lection through the parallel use of the same single-nucleotide polymorphisms and genomic loci, to a m

22 Single-nucleotide polymorphisms and locus amplification

23 Single-nucleotide polymorphisms and structural variants

24 CD39 is regulated via single-nucleotide-polymorphisms and upon activation of a

25 iously described polygenic risk score (N=929 single-nucleotide polymorphisms) and tested for an assoc

26 atness), a polygenic risk score (based on 90 single-nucleotide polymorphisms), and colonoscopy histor

27 Single nucleotide polymorphism- and metagenomic assembly

28 ffect of earlier puberty timing based on 203 single nucleotide polymorphisms applied to genome wide a

29 Single nucleotide polymorphisms are widely associated wi

30 PEX glaucoma-associated single-nucleotide polymorphisms are located in and affec

31 Single nucleotide polymorphism array analysis revealed t

32 e observed when comparing CNV Radar calls to single nucleotide polymorphism array results from acute

33 combination with genotype data generated by single-nucleotide polymorphism arrays and genotyping by

34 functional differences, we used rs2000999, a single nucleotide polymorphism associated with haptoglob

35 DeS3D, to identify the functional impacts of single nucleotide polymorphisms associated with AD (p <

36 arly revealed that almost half of the top 50 single nucleotide polymorphisms associated with estimate

37 acrophages from patients with IBD carrying a single-nucleotide polymorphism associated with the disea

38 We genotyped 21 single-nucleotide polymorphisms associated with atrial f

39 A set of 32 single-nucleotide polymorphisms associated with ischemic

40 Single-nucleotide polymorphisms associated with low- and

41 Single-nucleotide polymorphisms associated with new-onse

42 We identified several single-nucleotide polymorphisms associated with new-onse

43 Two single-nucleotide polymorphisms associated with P-gp act

44 Single-nucleotide polymorphisms associated with thyroid

45 In addition, we analyzed single nucleotide polymorphism association data for GDF1

46 (MAGMA), addresses this issue by aggregating single nucleotide polymorphism associations to nearest g

47 By single nucleotide polymorphism-based and sib-pair analys

48 We discuss how the single nucleotide polymorphism-based estimates of herita

49 The single nucleotide polymorphism-based heritability of ove

50 We developed a polygenic single nucleotide polymorphism-based predictor of LV mas

51 We found that a prevalent nonsynonymous single-nucleotide polymorphism (C/T, rs2034310) of the h

52 lter protein binding, it has been shown that single nucleotide polymorphisms can affect RNA secondary

53 A secondary structure, and here we show that single nucleotide polymorphisms can affect RNA-protein i

54 es TDP2-catalyzed TOP2-DPC removal, and TDP2 single nucleotide polymorphisms can disrupt the TDP2-Ubi

55 Six puberty-related single-nucleotide polymorphisms (combined into a weighte

56 Single nucleotide polymorphism data were produced from a

57 We apply our Bayesian GWAS method to single nucleotide polymorphisms data collected from a po

58 Single-nucleotide polymorphisms-dense regions support a

59 e (n = 20) bulk segregants revealed ~900,000 single nucleotide polymorphisms distributed across C. mo

60 covariance among individuals, and decomposes single-nucleotide polymorphism effects as either additiv

61 th sites of differential methylation or with single nucleotide polymorphisms exhibiting significant i

62 Using a common set of 61,974 single-nucleotide polymorphisms found in cattle genomes

63 o assess the additive contribution of common single nucleotide polymorphisms from genome-wide associa

64 t cultivars that were genotyped with 327 609 single-nucleotide polymorphisms generated by genotyping-

65 A 27-single-nucleotide polymorphism genetic risk score define

66 Finally, analysis of associated single-nucleotide polymorphisms genetically linked the D

67 Comparison of single-nucleotide polymorphism genotypes shows strong si

68 subjects with cardiometabolic disease, a 32-single-nucleotide polymorphism GRS was a strong, indepen

69 n mu opioid receptor gene, notably the A118G single nucleotide polymorphism, have been linked to indi

70 us sequence typing (cgMLST) and high-quality single nucleotide polymorphism (hqSNP) analysis of the s

71 a canephora, evaluated in two locations, and single nucleotide polymorphisms identified by Genotyping

72 Single nucleotide polymorphisms identified by whole geno

73 generated based on significantly associated single nucleotide polymorphisms identified from literatu

74 icant after conditioning on the common index single-nucleotide polymorphism identified by previous ge

75 -fold cross-validation summaries out to 1000 single-nucleotide polymorphisms identified optimal predi

76 In humans we identified a rare missense single nucleotide polymorphism in the BMP type 1 recepto

77 The rs12608932 single nucleotide polymorphism in UNC13A is associated w

78 In this study, we investigated whether single nucleotide polymorphisms in MHCII-DRB regulatory

79 Using 121 single nucleotide polymorphisms in MR, implemented throu

80 MtBNN, to quantify the deleterious impact of single nucleotide polymorphisms in non-coding genomic re

81 Finally, single nucleotide polymorphisms in the human genome that

82 found several, known and new, non-synonymous single nucleotide polymorphisms in the propeller region

83 xamined the effect modifications by selected single nucleotide polymorphisms in vitamin D-related gen

84 Single-nucleotide polymorphisms in the capsule biosynthe

85 vel, which enables tracking of low levels of single-nucleotide polymorphisms in the population over t

86 local lesions in genomes to identify induced single-nucleotide polymorphisms in the three homeologs o

87 t (based on genotyping of 33 risk-associated single nucleotide polymorphisms) in addition to the stan

88 ested six P-value thresholds (0.05-0.50) for single nucleotide polymorphisms included in the ADPRS.

89 de polymorphisms, whereas an additional CD82 single nucleotide polymorphism increased the risk for ca

90 Single nucleotide polymorphisms, insertion and deletions

91 ION flowcell, enabling accurate detection of single-nucleotide polymorphisms, insertions and deletion

92 Among HT African-Americans, three of the 12 single nucleotide polymorphisms interrogated for the SNX

93 Third, our sequencing analyses reveal a single nucleotide polymorphism introducing a premature s

94 Six correlated single nucleotide polymorphisms located in a brain-expre

95 ith median pairwise distance of 8 (IQR 4-13) single nucleotide polymorphisms; low diversity between c

96 tudy design based on a curated list of 3,295 single nucleotide polymorphisms mapped to 358 genes to t

97 A total of 178 single nucleotide polymorphism markers were used to eval

98 udies, such as Double Digest RAD-seq derived Single-Nucleotide Polymorphism markers.

99 correlation of the most strongly associated single-nucleotide polymorphism minor allele with increas

100 he observed increase in haplotype-associated single-nucleotide polymorphisms mirroring the increasing

101 Indeed, height-associated single nucleotide polymorphisms near genes encoding othe

102 Single-nucleotide polymorphisms near the ILRUN (inflamma

103 s widely, which may be due to non-synonymous single nucleotide polymorphisms (nsSNPs) within the AT1R

104 Patients were genotyped for rs4680, a single nucleotide polymorphism of COMT, and randomly all

105 in patients on hemodialysis with rs855791, a single nucleotide polymorphism of the TMPRSS6 gene that

106 ersus 50 min approximately for filtering the single nucleotide polymorphisms of a WGS Human sample).

107 nd the epigenome in a mouse model carrying a single-nucleotide polymorphism of the brain-derived neur

108 side]) to assess the impact of an identified single nucleotide polymorphism on BP.

109 ns we characterize the genome-wide effect of single nucleotide polymorphisms on HuR binding and show

110 e also find some evidence that the effect of single nucleotide polymorphisms on protein binding might

111 and class I alleles A*24 and B*39 and eight single nucleotide polymorphisms outside the HLA region w

112 The polygenic risk score derived from 112 single-nucleotide polymorphisms (p<5 x 10(-5)) showed th

113 onal genome wide association study using 60k Single Nucleotide Polymorphism panels.

114 Remarkably, single nucleotide polymorphisms present at nearly 20% in

115 Genotypes of 33 single nucleotide polymorphisms previously assigned to t

116 d and analyzed mice homozygous for these two single-nucleotide polymorphisms, Rabl2L119F (rs80006029)

117 pressing genes with high-density genome-wide single nucleotide polymorphisms, reflecting a comprehens

118 d fasting insulin, comprising 65, 43, and 13 single nucleotide polymorphisms, respectively.

119 an NLRP1 haplotype with asthma for which the single nucleotide polymorphism rs11651270 (M1184V) indiv

120 Recent evidence associates a single nucleotide polymorphism rs174547 within the FADS1

121 NV) generates HP1 and HP2 alleles, while the single-nucleotide polymorphism rs2000999 influences thei

122 ciation with survival at chromosome 12 (lead single nucleotide polymorphism rs2242367, p=7.5 x 10(-10

123 n on chromosome 18 upstream of ATP8B1 (index single nucleotide polymorphism rs2571244, minor allele f

124 Previously, we discovered a single nucleotide polymorphism (rs2869462) associated wi

125 Lead single-nucleotide polymorphism rs3211938 at CD36 was com

126 ession by binding to the SCZ-associated SNP (single nucleotide polymorphism) rs5011218, which affects

127 in a TLR2/1-dependent manner, using the TLR1 single-nucleotide polymorphism rs5743618 (1805G/T) as a

128 which reached genome-wide significance (lead single-nucleotide polymorphism, rs59532114; P = 2.35E-08

129 e identified a nonsynonymous coding variant, single nucleotide polymorphism rs61753924, which causes

130 The single nucleotide polymorphism rs7804356 located in the

131 isms identified optimal prediction with a 44 single-nucleotide polymorphism score and cutoff at the 3

132 roprotein convertase subtilisin/kexin type 9 single-nucleotide polymorphisms, serum proprotein conver

133 The OPRM1 A118G single nucleotide polymorphism (SNP rs1799971) gene vari

134 genotypes in outbred full-sib families from single nucleotide polymorphism (SNP) array and genotype-

135 We leveraged exome-sequence and single nucleotide polymorphism (SNP) array data from 29,

136 rabian horses from 12 countries using equine single nucleotide polymorphism (SNP) arrays and whole-ge

137 characterization of a lncRNA that harbors a single nucleotide polymorphism (SNP) associated with T1D

138 The lead single nucleotide polymorphism (SNP) at 16p12.3 is rs781

139 Traditional single nucleotide polymorphism (SNP) genome-wide associa

140 Dense single nucleotide polymorphism (SNP) genotyping across t

141 A genome wide association study identified a single nucleotide polymorphism (SNP) located in a homolo

142 nguished resistant and susceptible bulks and single nucleotide polymorphism (SNP) markers from these

143 sing nine microsatellite markers and > 9,000 single nucleotide polymorphism (SNP) markers generated u

144 d and used to detect and position sex-linked single nucleotide polymorphism (SNP) markers in 19 famil

145 ge, and the dominant HTTLPR with the rs25531 single nucleotide polymorphism (SNP) model, explained th

146 The G allele of the lead risk single nucleotide polymorphism (SNP) rs67180937 was asso

147 iation studies were combined to test a large single nucleotide polymorphism (SNP) set for association

148 aneous estimation of the genetic effect of a single nucleotide polymorphism (SNP), as well as non-gen

149 havioral rhythms, and the common MTNR1B risk single nucleotide polymorphism (SNP), rs10830963, associ

150 nalysis of EAA in AUD revealed a significant single nucleotide polymorphism (SNP), rs916264 (p = 5.43

151 gh sequencing coverage to detect significant single nucleotide polymorphism (SNP)-trait associations,

152 iform cortex were associated with the UNC13A single nucleotide polymorphism (SNP; p = 0.045 and p = 0

153 genome-wide association study and estimated single nucleotide polymorphisms (SNP) heritability for a

154 Human lung gene expression and single nucleotide polymorphisms (SNP) in neuroplasticity

155 the relationship between those features and single nucleotide polymorphisms (SNP) in the pig genome.

156 alyze host and symbionts based on bi-allelic single nucleotide polymorphisms (SNP) markers identified

157 to its continuous evolution with over 10,000 single nucleotide polymorphisms (SNP) variants in many s

158 Despite their success, the individual single-nucleotide polymorphism (SNP) analysis approach a

159 total n = 4050, of whom 2431 had genome-wide single-nucleotide polymorphism (SNP) data).

160 way level, and estimating heritability using single-nucleotide polymorphism (SNP) data.

161 ng (WGS) of tumor-normal pairs (n = 135) and single-nucleotide polymorphism (SNP) genotyping of prima

162 ng, and polygenic score analyses, as well as single-nucleotide polymorphism (SNP) heritability and ge

163 a structure (cell-count or relatedness), and single-nucleotide polymorphism (SNP) marker effects, imp

164 We found differences in the degree of single-nucleotide polymorphism (SNP) occurring in cells

165 ent report suggested that the rs73185306 C/T single-nucleotide polymorphism (SNP) represents a favora

166 hort, stratified by FADS genotype at the key single-nucleotide polymorphism (SNP) rs174537, to metabo

167 At the chromosome 6p21.3 locus, the single-nucleotide polymorphism (SNP) rs56151658 (8 kb fr

168 sion (POPH) was previously associated with a single-nucleotide polymorphism (SNP) rs7175922 in aromat

169 s genome-wide association study identified a single-nucleotide polymorphism (SNP) signal across the g

170 sativa (rice), we isolated an OsPIP1;3 gene single-nucleotide polymorphism (SNP) that is mostly expr

171 We further calculated the single-nucleotide polymorphism (SNP)-based heritability

172 technology has made it practical to estimate single-nucleotide polymorphism (SNP)-heritability among

173 n (LAMP) for the detection of the BRAF V600E single-nucleotide polymorphism (SNP).

174 18 genome-wide significant (P < 5 x 10(-8)) single-nucleotide polymorphisms (SNP) for self-reported

175 Using this method, we selected two sets of single-nucleotide-polymorphism (SNP) genetic variants (S

176 sly been made to comprehensively analyse the single nucleotide polymorphism (SNPs) of the BLM gene.

177 variant at four known loci to fewer than 10 single nucleotide polymorphisms (SNPs) (FAIM2, GNPDA2, M

178 A haplotype defined by six single nucleotide polymorphisms (SNPs) (rs208307, rs2083

179 anscription factors (TFs) and a total of 514 single nucleotide polymorphisms (SNPs) among the identif

180 ch, we tested the hypothesis that individual single nucleotide polymorphisms (SNPs) and gene-level va

181 associations between genotypic data such as single nucleotide polymorphisms (SNPs) and imaging quant

182 We found 41 genome-wide significant single nucleotide polymorphisms (SNPs) and independently

183 The integration between single nucleotide polymorphisms (SNPs) and miRNAs has be

184 i population based on a battery of autosomal single nucleotide polymorphisms (SNPs) and short tandem

185 The functional genes or single nucleotide polymorphisms (SNPs) are not obvious d

186 Individualizing single nucleotide polymorphisms (SNPs) are often conserv

187 ion studies (GWASs) have identified numerous single nucleotide polymorphisms (SNPs) associated with b

188 ssociation studies (GWAS) have identified 14 single nucleotide polymorphisms (SNPs) associated with c

189 bosis (INVENT) consortium to examine whether single nucleotide polymorphisms (SNPs) associated with G

190 have led to comprehensive identification of single nucleotide polymorphisms (SNPs) associated with p

191 In this study, we first identify single nucleotide polymorphisms (SNPs) associated with p

192 Many single nucleotide polymorphisms (SNPs) associated with t

193 We previously identified five single nucleotide polymorphisms (SNPs) at four susceptib

194 Ancestry informative single nucleotide polymorphisms (SNPs) can identify biog

195 Despite the supergene's size, only 142 single nucleotide polymorphisms (SNPs) consistently dist

196 es) using independent genomewide significant single nucleotide polymorphisms (SNPs) for each trait.

197 We tested an array of 79 single nucleotide polymorphisms (SNPs) for their utility

198 The assay includes 5000 single nucleotide polymorphisms (SNPs) from euchromatic

199 eration sequencing (NGS) approach to examine single nucleotide polymorphisms (SNPs) from virus passag

200 IL33 single nucleotide polymorphisms (SNPs) have been reprodu

201 on between the cumulative effect of multiple single nucleotide polymorphisms (SNPs) in a particular g

202 Single nucleotide polymorphisms (SNPs) in Apolipoprotein

203 We found 29 single nucleotide polymorphisms (SNPs) in FTO significan

204 We investigated whether single nucleotide polymorphisms (SNPs) in IFNG may be as

205 Both vitamin D deficiency and single nucleotide polymorphisms (SNPs) in the gene encod

206 Single nucleotide polymorphisms (SNPs) in the gene encod

207 cent findings that multiple loss of function single nucleotide polymorphisms (SNPs) in the human gene

208 o based on their parental inbred lines using single nucleotide polymorphisms (SNPs) markers obtained

209 riation and clinical conditions suggest that single nucleotide polymorphisms (SNPs) might correlate w

210 idual effects of three commonly investigated single nucleotide polymorphisms (SNPs) of the ABCB1 gene

211 ue dataset with 1087 subjects and identified single nucleotide polymorphisms (SNPs) regulating their

212 good dietary adherence were genotyped for 95 single nucleotide polymorphisms (SNPs) related to energy

213 At the vast majority of these loci, the lead single nucleotide polymorphisms (SNPs) reside in noncodi

214 ociation studies have identified hundreds of single nucleotide polymorphisms (SNPs) that are associat

215 Candidate molecular targets include seven single nucleotide polymorphisms (SNPs) that are suscepti

216 mples were genotyped with 46,818 polymorphic single nucleotide polymorphisms (SNPs) using DArTseq.

217 Single nucleotide polymorphisms (SNPs) were assessed usi

218 -association threshold (p < 5 x 10(- 8)), 33 single nucleotide polymorphisms (SNPs) were detected for

219 Single nucleotide polymorphisms (SNPs) were determined b

220 Strongly associated single nucleotide polymorphisms (SNPs) were located in r

221 oach not only provided accurate selection of single nucleotide polymorphisms (SNPs) with comparable o

222 mellitus and quality control, association of single nucleotide polymorphisms (SNPs) with log-transfor

223 we wondered whether these iPSC-lines carried single nucleotide polymorphisms (SNPs) within genes that

224 burden, although the effects were driven by single nucleotide polymorphisms (SNPs) within the APOE l

225 -wide association studies (GWAS) to identify single nucleotide polymorphisms (SNPs), associated with

226 ed next generation sequencing to sequence 87 single nucleotide polymorphisms (SNPs), coding and splic

227 polipoprotein B to identify lipid-associated single nucleotide polymorphisms (SNPs).

228 48 000 genotyped single nucleotide polymorphisms (SNPs).

229 The 8 PACG-associated single nucleotide polymorphisms (SNPs; rs11024102 at PLE

230 rly designed with thousands and thousands of single-nucleotide polymorphisms (SNPs) (big p) genotyped

231 w genome-wide association studies-identified single-nucleotide polymorphisms (SNPs) affect remote gen

232 351,824 Single-Nucleotide Polymorphisms (SNPs) and 38 imputed Hu

233 ral sequences showed transient variations in single-nucleotide polymorphisms (SNPs) and constant turn

234 the frequency of TLR2, TLR3, TLR4, and TLR9 single-nucleotide polymorphisms (SNPs) and investigated

235 Here we utilize thousands of genome-wide single-nucleotide polymorphisms (SNPs) and mitochondrial

236 bit the highest enrichment of SSc-associated single-nucleotide polymorphisms (SNPs) and predict the d

237 play the role of the primary data for AdaPT; single-nucleotide polymorphisms (SNPs) are selected beca

238 s (GWAS) have been invaluable in identifying single-nucleotide polymorphisms (SNPs) associated with i

239 studies (GWASs) have identified at least 10 single-nucleotide polymorphisms (SNPs) associated with p

240 ypertension or hypotension and >1,477 common single-nucleotide polymorphisms (SNPs) being associated

241 lution by comparing frequency differences in single-nucleotide polymorphisms (SNPs) between populatio

242 Polygenic risk scores comprising millions of single-nucleotide polymorphisms (SNPs) could be useful f

243 We obtain 925,854 high-quality single-nucleotide polymorphisms (SNPs) enabling the refi

244 ined' diagnosis of FMD were genotyped for 18 single-nucleotide polymorphisms (SNPs) from 14 candidate

245 We assessed germline single-nucleotide polymorphisms (SNPs) in 180 mCRC patie

246 ate GWASs of 100,000 individuals and 500,000 single-nucleotide polymorphisms (SNPs) in 5.6 h on a sin

247 We identified significant enrichment of risk single-nucleotide polymorphisms (SNPs) in active regulat

248 DESIGN, SETTING, AND PARTICIPANTS: Single-nucleotide polymorphisms (SNPs) in HMGCR, NPC1L1,

249 We hypothesized that functional single-nucleotide polymorphisms (SNPs) in inflammasome p

250 Two single-nucleotide polymorphisms (SNPs) in Orai1 have bee

251 we estimated the age of more than 45 million single-nucleotide polymorphisms (SNPs) in the human geno

252 (WGS) technology allow for the detection of single-nucleotide polymorphisms (SNPs) in the pathogen g

253 e constructed haplotype genetic scores using single-nucleotide polymorphisms (SNPs) known to be assoc

254 have revealed that 88% of disease-associated single-nucleotide polymorphisms (SNPs) reside in noncodi

255 To define the functionality of single-nucleotide polymorphisms (SNPs) systematically, w

256 of 2149 healthy Finns, we identified sets of single-nucleotide polymorphisms (SNPs) that cluster with

257 Here, we use 3057 genome-wide single-nucleotide polymorphisms (SNPs) to evaluate popul

258 ed from saliva (~38%) or blood (~62%) and 24 single-nucleotide polymorphisms (SNPs) were genotyped.

259 'Nebbiolo'-specific single-nucleotide polymorphisms (SNPs) were identified s

260 We found 80 single-nucleotide polymorphisms (SNPs) with false discov

261 pants with available 25OHD levels, retaining single-nucleotide polymorphisms (SNPs) with minor allele

262 sociation studies (GWAS) have linked IGF2BP2 single-nucleotide polymorphisms (SNPs) with type 2 diabe

263 showed distinct positional distributions of single-nucleotide polymorphisms (SNPs) within and outsid

264 egments of DNA containing clusters of linked single-nucleotide polymorphisms (SNPs), called haplotype

265 the genetic basis, including 1) deleterious single-nucleotide polymorphisms (SNPs), in-frame indels,

266 number of potentially geographic-associated single-nucleotide polymorphisms (SNPs), rather than geog

267 ery of potentially causal disease-associated single-nucleotide polymorphisms (SNPs), thus helping fin

268 ed where the genomic distance was 5 or fewer single-nucleotide polymorphisms (SNPs), whereas reinfect

269 xamining associations between phenotypes and single-nucleotide polymorphisms (SNPs).

270 ltiple sequence alignment which is mined for single-nucleotide polymorphisms (SNPs).

271 ion on type 2 diabetes, based on independent single nucleotide polymorphisms strongly associated (p =

272 (RLP/KSeq) leads to detection of informative single nucleotide polymorphisms that are linked to the t

273 lysis of Yp pagP gene sequences identified a single-nucleotide polymorphism that results in a prematu

274 ased on 16 independent candidemia-associated single-nucleotide polymorphisms that affect monocyte-der

275 tified and validated (in 5 European cohorts) single-nucleotide polymorphisms that affect risk of alco

276 ome-wide association studies have identified single-nucleotide polymorphisms that are associated with

277 Across these 14 single-nucleotide polymorphisms there was evidence of si

278 smission clusters using a 10 non-recombinant single nucleotide polymorphism threshold, tested for clu

279 ion triggered such rapid adaptation, we used single nucleotide polymorphisms to characterize patterns

280 me 10, causing both structural variation and single-nucleotide polymorphism to deviate from genome-wi

281 re since the first node is one specific SNP (Single Nucleotide Polymorphism) variant and the end is d

282 From this panel, we identified 355 050 single nucleotide polymorphism variants and quantified t

283 We identified 79 unique variance-controlling single nucleotide polymorphisms (vSNPs) from the sequenc

284 This single nucleotide polymorphism was expressed in human em

285 ele-specific PCR targeting outbreak-specific single nucleotide polymorphisms was applied to 290 isola

286 Similarly, the presence of FcyR single nucleotide polymorphisms was unimpactful.

287 (SNP) Chip containing 956 candidate EoE risk single-nucleotide polymorphisms was used to genotype 627

288 NA and other transcripts in proximity of the single nucleotide polymorphism were unaltered.

289 equence repeats, large repeat sequences, and single nucleotide polymorphisms were identified, which a

290 Coding single nucleotide polymorphisms were sequenced in candid

291 Single nucleotide polymorphisms were used to assess micr

292 A total of 779 subjects and 1,192,414 single-nucleotide polymorphisms were available for PRS-a

293 Before linkage analysis, single-nucleotide polymorphisms were pruned and clumped.

294 Up to 94 single-nucleotide polymorphisms were used as instrumenta

295 Loci were identified as clusters of single nucleotide polymorphisms where frequencies of the

296 production was influenced by two human CD82 single nucleotide polymorphisms, whereas an additional C

297 gue that the derived allele of the rs1800407 single nucleotide polymorphism, which produces a hypomor

298 Studies regarding the association of single nucleotide polymorphisms with AVNFH, transcriptom

299 ificantly, enriched in the genes overlapping single nucleotide polymorphisms with genome-wide signifi

300 sociation mapping approach to identify SNPs (single nucleotide polymorphisms) with significant associ