ライフサイエンスコーパス: genetic structure

1 stand dispersal dynamics and to characterise genetic structure.

2 ntify a tripartite, ancient, Khoesan-related genetic structure.

3 ute to population demography and patterns of genetic structure.

4 common approach for understanding population genetic structure.

5 adaptation were responsible for the observed genetic structure.

6 nvestigated the impact of breeding timing on genetic structure.

7 general understanding of the factors driving genetic structure.

8 eward post-glacial shift revealed in current genetic structure.

9 istance (IBD) primarily explained population genetic structure.

10 luding genetic diversity loss and changes in genetic structure.

11 injury characteristics as well as population genetic structure.

12 l and gene flow continue to shape population genetic structure.

13 igration and post-glacial range expansion on genetic structure.

14 ity to resolve subtle patterns of population genetic structure.

15 ction on codon use, and only weak geographic genetic structure.

16 specific nesting groups, despite significant genetic structure.

17 nvestigation of population history and human genetic structure.

18 -term ecological trajectories and population genetic structure.

19 on microbial population structures and their genetic structures.

20 ructing phylogenies, and studying population genetic structures.

21 wers to easily see several features of human genetic structure: (1) most variants are rare and geogra

22 from outside the New World affected (1) the genetic structure, (2) the admixture profile, (3) the de

23 provides a high-resolution view of parasite genetic structure across a large country in Africa and p

24 PIMMS43 genetic structure across African Plasmodium falciparum p

25 Here we illustrate fine-scale genetic structure across Ireland that follows geographic

26 for leveraging the variability in the local genetic structure across populations.

27 typed at 19 microsatellite loci, we analyzed genetic structure across the range using clustering anal

28 We found strong genetic structure across the region, and significant iso

29 ellite analyses did not identify significant genetic structure across the seven shallow M. cavernosa

30 sing the 2bRAD approach to assess fine-scale genetic structure across these sites.

31 tigated the degree of congruence between the genetic structures across Europe of two evolutionary and

32 the four lineages, PPRV-IV showed pronounced genetic structuring across the region; however, haplotyp

33 ill impose barriers to dispersal and promote genetic structuring across the species range.

34 d by a dramatic temporal shift in population genetic structure after the onset of European settlement

35 We detected strong genetic structure along the Mediterranean for I. fascicu

36 rgely unexplained, the punctual detection of genetic structure also raises questions regarding the ex

37 Weak spatial genetic structure among adults suggests high historical

38 genetic cluster across the range, with weak genetic structure among recently geographically isolated

39 netic differentiation and fine-scale spatial genetic structure among recruits in fragments compared w

40 by a low but significant level of population genetic structure among symbiont populations inhabiting

41 Our results show an overall weak genetic structure among the populations, indicating a hi

42 ee mouse populations of increasingly complex genetic structure: an F2 intercross, a heterogeneous sto

43 Population genetic structure, analysed using DNA from dormant eggs

44 Genetic structure analyses indicate that among Africans,

45 g the various hominin lineages, we performed genetic structure analyses to provide a comparison of ge

46 Genetic structure analysis (UPGMA) and various measures

47 A genome-wide genetic structure analysis of southern African populatio

48 polymorphisms (SNPs) to evaluate population genetic structure and assess the levels of relatedness a

49 This study characterized genetic structure and assessed horizontal and vertical c

50 However, little is known about the genetic structure and changes of prehistoric populations

51 cular markers to characterize the population genetic structure and connectivity of Ipomoea purpurea (

52 o understand how these factors have affected genetic structure and connectivity of Siberian roe deer,

53 We assessed range-wide genetic structure and contemporary gene flow in the thor

54 ossing) have divergent effects on population genetic structure and could thereby broadly influence tr

55 tal of 340 individuals were tested for their genetic structure and degree of inbreeding.

56 r results provide detailed insights into the genetic structure and demographic history of the diverse

57 s of current drainages can act as drivers of genetic structure and demographic processes in riverine

58 Nn is a measure of within-population spatial genetic structure and depends strongly on the dispersal

59 tional Animal Germplasm Program and explores genetic structure and differences among 19 pig populatio

60 l/biogeographic processes driving population genetic structure and divergence.

61 Our results argue that surveys of eelgrass genetic structure and diversity at decadal scales can pr

62 nt can be an important factor in driving the genetic structure and diversity in An. cruzii population

63 When and where animals breed can shape the genetic structure and diversity of animal populations.

64 A favourable genetic structure and diversity of behavioural features

65 rtative mating, culture can shape population genetic structure and diversity.

66 We investigated the genetic structure and gene flow of E. serotinus across t

67 Here, we examine the genetic structure and genomic diversification of natural

68 However, the reproductive mode, genetic structure and host adaptation of phylloxera in v

69 flow by the quantification of regional-scale genetic structure and isolation by distance among 18 pop

70 To study the genetic structure and kin relations in CWC communities,

71 Previous work has identified genetic structure and morphological, behavioral, and phy

72 pecies, and unveiled for the first time that genetic structure and pathogen composition in different

73 tugal) were chosen to examine the population genetic structure and phylogeographic history of the cos

74 Here, we examined the genetic structure and phylogeographic patterns of K. oce

75 e found evidence for moderately low regional genetic structure and reduced gene flow towards the rang

76 nnectivity simulations) to assess population genetic structure and self-recruitment in a broadcast-sp

77 is sufficient to explain the high levels of genetic structure and self-recruitment.

78 d on genome-wide SNPs revealed a north-south genetic structure and signatures of selection were ident

79 idual) to investigate patterns of population genetic structure and species status of three different

80 Further, we find a large overlap in genetic structure and the distribution of variants betwe

81 Western North America, we observe geographic genetic structure and the genetic signature of multiple

82 that result in low levels of spatio-temporal genetic structure and the maintenance of genetic diversi

83 eritage has shaped how the cell controls the genetic structure and the physical behavior of its organ

84 ariant sites SNPs that were used to estimate genetic structure and to identify gene candidates under

85 responded to: (a) a strong signal of spatial genetic structure and, (b) a cryptic signal of host diff

86 me being used in this setting to study other genetic structures and functions to answer fundamental q

87 ng systems and their influence on population genetics structure and adaptive potential.

88 le of environmental heterogeneity in shaping genetic structure, and access the footprints of local ad

89 i associated with colony morphology, cryptic genetic structure, and apparent bleaching susceptibility

90 n they incorporate information on population genetic structure, and concomitantly, local adaptation.

91 ed regarding its phylogenomic relationships, genetic structure, and diversification.

92 that populations of C. ciliata have obvious genetic structure, and genetic differentiation is not ca

93 y the pollen flow and dispersal, the spatial genetic structure, and the effective size of a populatio

94 related with individual-level geographic and genetic structure, and with population-level differences

95 Here, present-day patterns of genetic structure are thought to be dictated by repeated

96 proach for investigating population-specific genetic structure as well as functionally mapping region

97 Genetic structure assessment, using several approaches,

98 the native European range had strong spatial genetic structure associated with geographic distance an

99 d Bayesian clustering highlighted the strong genetic structure at all scales, between the Black Sea a

100 In addition, genetic structure at neutral loci reflected extensive ge

101 s guttatus as a case study for understanding genetic structure at three spatial scales.

102 ed, the congruence between host and pathogen genetic structures at the within-species level has recei

103 Today's genetic structure began to develop by 5,800 BP, followed

104 Our results demonstrate that genetic structure between populations is not just highly

105 also pointed to the presence of significant genetic structure between sympatric An. cruzii populatio

106 Genetic data showed contrasting patterns of genetic structure between the two lineages, different de

107 exes, which could occur if sex structure and genetic structure both occur within populations.

108 n conclusion, the high diversity and lack of genetic structure can be explained by a historically lar

109 adaptive walks on a fitness landscape, whose genetic structure can be probed by experiments.

110 Understanding population genetic structure can help us to infer dispersal pattern

111 e highly vagile, our analyses reveal spatial genetic structures comparable to those documented for an

112 -based approaches that account for ancestral genetic structure, complex haplotypes, gene-gene interac

113 Our study aims to establish (1) the genetic structure, connectivity and signs of bottlenecks

114 symbiont, and microbial references revealed genetic structure consistent with recent host-symbiont c

115 Significant genetic structure (correlating with geography) was detec

116 Analyses for genetic structure depicted structuring between species,

117 Limited genetic structure detected in all ice-affected species a

118 s across the world shows that the population genetic structure differs markedly between the main zoon

119 ispersal is known to strongly affect spatial genetic structure during range expansions, the resulting

120 lite and a mitochondrial markers to evaluate genetic structure, estimate effective population size an

121 ltural activity in Brazil shaped its spatial genetic structure, facilitating ecological divergence an

122 even microsatellite loci to characterize the genetic structure for 24 populations of Cirsium pitcheri

123 Our population genomic data revealed strong genetic structure for B. oxycarpa sampled across banks o

124 arliest breeders had significantly different genetic structure from the latest breeders.

125 We found moderate genetic structure (Fst=0.14), and a north-south pattern

126 ena requires comparative studies integrating genetic structure, functional traits and dispersal const

127 We examined the population genetic structure, genetic diversity and demographic his

128 ets can provide high-resolution estimates of genetic structure, genetic diversity, gene flow, and evo

129 entation on genetic diversity, gene flow and genetic structure has rarely been investigated in Bornea

130 ; however, its mating system and patterns of genetic structure have been rarely explored.

131 ion and their integration with intraspecific genetic structure have been underexplored in phylogeogra

132 fluence of ancient trading networks on their genetic structure have remained elusive.

133 ain and Ireland are known to show population genetic structure; however, large swathes of Scotland, i

134 Population genetic structures illustrate evolutionary trajectories

135 ty trajectories, showing that the population genetic structure imposed by partial selfing affected th

136 By characterizing genetic structure in a freshwater fish species (Hollandi

137 ts provide insight into the spatial scale of genetic structure in a widespread plant species, and dem

138 We observe that genetic structure in Africa is broadly correlated not on

139 ses and limited spatial processes, affecting genetic structure in an otherwise panmictic population o

140 orphisms were used to assess microgeographic genetic structure in An. cruzii populations in a low-end

141 other cetaceans, we found a complete lack of genetic structure in both maternally and biparentally in

142 ary environments have all shaped patterns of genetic structure in E. henryi, and, in fact, changes in

143 Our results identified regional genetic structure in E. verrucosa partitioned between po

144 on, and quantified within-population spatial genetic structure in four populations.

145 enturies is sufficient to produce detectable genetic structure in human populations.

146 lankton may generate and maintain population genetic structure in marine microbes despite global-scal

147 lyses by allowing quantification of temporal genetic structure in organisms that generate variation v

148 ng rates in four populations and the spatial genetic structure in six populations.

149 a longitudinal design were tested to assess genetic structure in sympatric An. cruzii populations an

150 assess genetic diversity, gene flow and the genetic structure in the Bornean tree shrew, Tupaia long

151 Moreover, the assemblies reveal a diverse genetic structure in the genome ends.

152 We analysed the fine-scale genetic structure in the mussel Mytilus galloprovinciali

153 past demographic history and contemporaneous genetic structure in the native area of the gastropod Tr

154 To investigate the genetic structure in the species, six North American urb

155 ndirect effects of eutrophication proxies on genetic structure in these lake populations and demonstr

156 We examined genetic structure in this diverse crop in Africa.

157 landscape along the riverbanks affected the genetic structure in this species.

158 al adaptive genetic variation and erosion of genetic structure in wild populations.

159 Natural processes have led to genetic structuring in wild populations.

160 hylogeographic structure, and the population genetic structure (in our AFLP dataset) was partly expla

161 within less than 250,000 years, we show that genetic structuring including the segregation of potenti

162 epths of tens of meters exhibits significant genetic structure, indicative of low population connecti

163 We estimated genetic diversity, spatial genetic structure, indirect contemporary pollen flow and

164 factors contribute to genetic divergence and genetic structure is a central question in ecology and e

165 Subsequent genetic structure is attributed to Pleistocene climatic

166 e isolation hypothesis proposes that spatial genetic structure is erased beyond the limits of short-d

167 An understanding of genetic structure is essential for answering many questi

168 Therefore, population genetic structure is shaped by heterogeneities in collec

169 mating patterns, which can affect population genetic structure, is important for correctly modeling p

170 d fragmentation, and that fine-scale spatial genetic structure may be a particularly useful indicator

171 This complex genetic structure may be the result of multiple evolutio

172 ns in the short term, whereas inbreeding and genetic structure may respond more strongly.

173 primarily driven by an isolation by distance genetic structure model (49% of genetic variance), with

174 alysis indicated some evidence of fine-scale genetic structuring, most likely due to limited seed dis

175 For both species, no evidence of genetic structuring, nor significant variation in geneti

176 w that the multispecies coalescent diagnoses genetic structure, not species, and that it does not sta

177 nce to the nearest village best explains the genetic structure observed.

178 the years prior to the 2017 hurricanes, with genetic structure occurring at the local and regional le

179 The phylogenetic distribution and population genetic structure of 51 clinical isolates from Northeast

180 We characterise the fine-scale genetic structure of a geographically-isolated populatio

181 Understanding the genetic structure of a population is essential to its co

182 to microevolution, defined by changes in the genetic structure of a population over short ecological

183 ation and geographic barriers on the spatial genetic structure of a widely dispersed and phylogenetic

184 the evidence for evolutionary changes in the genetic structure of anatomically modern humans in recen

185 Critically, the population genetic structure of bacterial hosts was chararacterized

186 Finally, the genetic structure of Caucasus populations highlights a r

187 y processes contributes to understanding the genetic structure of continuously distributed marine spe

188 ectivity than elsewhere, agreeing with known genetic structure of coral reef organisms.

189 s and gives more complete information on the genetic structure of D. pini, D. sibiricus, and D. super

190 daptation in invaded regions, we studied the genetic structure of D. suzukii collected across Italy,

191 The genetic structure of domestic sheep strains could not be

192 ite markers provide valuable information for genetic structure of E.(M.) onukii in Chinese tea planta

193 Population genetic structure of E.(M.) onukii was detected using St

194 warming scenarios, which could influence the genetic structure of extant populations.

195 gorithm specifically designed to exploit the genetic structure of full-sib families.

196 Here we examined the range-wide genetic structure of historic and modern populations usi

197 ese genetic data, we evaluate the population genetic structure of historical A. varius and A. zeteki

198 loped microsatellite markers to describe the genetic structure of host populations and assess the rel

199 er, little is known about the phenotypic and genetic structure of internalizing psychopathology in ch

200 Here, we study the fine-scale genetic structure of its population, and the genetic imp

201 The distribution and genetic structure of koala populations has been heavily

202 Thus, patterns of genetic structure of L. auriculata can result from both

203 We provided a genetic structure of lnc18q22.2 showing an extended exon

204 Studies of the genetic structure of LOX-1 have also uncovered various g

205 In this study, we investigated the genetic structure of M. salmoides from 20 wild populatio

206 etic variations and established a population genetic structure of major goldfish strains.

207 rios of forest dynamics through time and the genetic structure of mammal species cooccurring in the c

208 erns to help in understanding the population genetic structure of Mexican ticks.

209 ial out-of-Africa expansion have altered the genetic structure of most of the world's human populatio

210 Little is known regarding the genetic structure of N. tenuis and the effect of histori

211 Here, we analyze the epidemiology and genetic structure of natural populations of an obligate

212 ap of Eurasia: we demonstrated complexity of genetic structure of Northern Eurasians, existence of Ea

213 play the primary role in shaping the spatial genetic structure of O. sinensis.

214 typing-by-sequencing approach to examine the genetic structure of one abundant caterpillar species, E

215 t isolation by distance does not explain the genetic structure of P. sativum subsp. elatius in its we

216 We examined reproductive mode and genetic structure of phylloxera by analyzing microsatell

217 Analyses of the spatial and genetic structure of plant pathogens offer valuable insi

218 n drivers for the contemporary diversity and genetic structure of plants in the Himalaya-Hengduan Mou

219 iation study datasets that aimed to find the genetic structure of platelet function and body mass ind

220 nservation measures is that connectivity and genetic structure of populations are poorly known.

221 Studies of the genetic structure of populations are still scarce for Ne

222 idence supports 21 ancestries that delineate genetic structure of present-day human populations.

223 asets can provide detailed insights into the genetic structure of prokaryotic genomes.

224 The extent to which the population genetic structure of S. epidermidis distinguishes commen

225 Comparison of the genetic structure of Siberian ethnicities and the geogra

226 ddress this gap, we evaluated the population genetic structure of the coral Montastraea cavernosa acr

227 Here, we analyzed the clonal and genetic structure of the cyclical parthenogenetic rotife

228 The broad-scale genetic structure of the European badger (Meles meles) i

229 c sites of integration and characterized the genetic structure of the gag region in each provirus.

230 Taken together, our data shed light on the genetic structure of the HHV-6A and HHV-6B integration l

231 This is the first study characterising the genetic structure of the invasive species D. suzukii in

232 construct changes in the temporal population genetic structure of the keystone zooplankton grazer, Da

233 y-generation hybrids is likely to impact the genetic structure of the natural hybrid zone on Mount Et

234 s, yet little is known about the spatial and genetic structure of the parasite population in that cou

235 g, and these tools rarely address the actual genetic structure of the population under study.

236 robable origin of this invasive species, the genetic structure of the population was compared against

237 ations were identified within the phenotypic/genetic structure of the Pseudomonas population, and bet

238 We hypothesize that the genetic structure of the species follows a hierarchical

239 The correlation between the genetic structure of the symbiont and that of its host w

240 umina OvineSNP50 array and characterised the genetic structure of these breeds.

241 nrecognized interspecific differences in the genetic structure of these cryptic keystone species.

242 refugia played distinct roles in shaping the genetic structure of these wasps.

243 population genetic diversity and population genetic structure of this pest in China, microsatellite

244 However, the genetic structure of this pest remains poorly understood

245 landscape characteristics that influence the genetic structure of this species across a spatially and

246 n approach, and apply it to characterize the genetic structure of thousands of strains from more than

247 We found that the underlying genetic structure of Varanus niloticus across Sahelian A

248 However, whether the genetic structure of vector populations impacts malaria

249 It is thought that diversity and genetic structure of viral populations determine the rap

250 by the inability to accurately describe the genetic structure of virus populations.

251 ification by humans has driven change in the genetic structure of wild lemurs.

252 to achieve deep understanding of the complex genetic structures of disease, and offer powerful tools

253 minary evidence for different phenotypic and genetic structures of internalizing disorder symptoms in

254 Such efforts will require exploiting the genetic structures of recently evolved halophytes, the g

255 The genetic structures of the SCA cohorts from Brazil and US

256 equencing provides a novel approach to study genetic structures of viral populations.

257 is indicates migratory culture may influence genetic structure on feeding grounds.

258 h understanding of the effects of population genetic structure on PSs is essential for translational

259 We also observed spatial genetic structure patterns congruent with oceanography.

260 uggesting bias arising from the population's genetic structure rather than from a direct genotype-phe

261 ults revealed the existence of a significant genetic structure separating populations according to th

262 of North America have had their contemporary genetic structure shaped by vicariant events, especially

263 More population genetic structure studies involving various C. parvum su

264 ongruent with empirical estimates of spatial genetic structure, suggesting that the pattern of disper

265 This modern genetic structure suggests a northwestern British or Iri

266 first, P. angustifolia has stronger neutral genetic structure than many forest trees (simple sequenc

267 st, nonnative populations had weaker spatial genetic structure that was not associated with environme

268 In contrast to the pronounced genetic structure, there was no evidence of inbreeding w

269 o determine genetic diversity and population genetic structure throughout its range.

270 ower for detecting increasingly finer-scaled genetic structure under the multispecies coalescent.

271 We inferred patterns of gene flow and genetic structure using 12 microsatellite markers.

272 Analyses of genetic structure using microsatellite variation reveals

273 compound, berberine, to these non-canonical genetic structures using UV-Vis and fluorescence spectro

274 Levels of genetic structure varied among species and emerged prima

275 AFLP loci was close to zero, and genomewide genetic structure was associated neither with species ab

276 associated with distance from shore, but no genetic structure was associated with bleaching.

277 A significant spatial genetic structure was detected for the adult plants (up

278 plants, and significant small-scale spatial genetic structure was detected within populations.

279 Additionally, although significant spatial genetic structure was found in all populations, biparent

280 Greater genetic structuring was found in England compared with c

281 multivariate models to assess gene flow and genetic structure, we identified one single group of jag

282 We found that community characteristics and genetic structure were influenced by a combination of co

283 pattern of occurrence, and displayed little genetic structure, while rare species were mainly charac

284 We detected significant genetic structure with an extraordinary disequilibrium o

285 We correlated genetic structure with ecological differentiation, diver

286 These SVs recover population genetic structure with high resolution, include an activ

287 d microsatellites to compare its patterns of genetic structure with the predominantly selfing and oft

288 indicated a good concordance of present-day genetic structure with the reported history of clam tran

289 on-by-environment explained 9.2-19.5% of the genetic structure, with c.

290 ity and dispersal confounds the inference of genetic structure, with multi-level sampling and spatial

291 vidual infections showed complex patterns of genetic structure, with variation not only in the number

292 ring across the zonal gradient showed strong genetic structuring, with the presence of at least two n

293 hypothesis by the analysis of gene flow and genetic structure within and among populations of the eu

294 es and the wild Przewalski's horse and found genetic structure within Eurasia in the Late Pleistocene

295 l is rampant with little evidence of spatial genetic structure within populations.

296 We observe genetic structure within Scandinavia, with diversity hot

297 A and microsatellites, revealed considerable genetic structure within the archipelago, suggestive of

298 here should be clear geographically coherent genetic structuring within one of the world's highest al

299 in the Sahel, with the expectation that the genetic structure would correspond to riverine drainage

300 also found many loci associated with cryptic genetic structure, yet relatively few loci associated wi