ライフサイエンスコーパス: recombination rate

1 ocused on the adaptive value of variation in recombination rate.

2 e and scope of population-level variation in recombination rate.

3 st variant types show a correlation with the recombination rate.

4 promoters is concomitant with an increase in recombination rate.

5 andidates in regions of high mutation or low recombination rate.

6 levels of recombination, Sir2 represses this recombination rate.

7 olution of genetic mapping is limited by the recombination rate.

8 as correlated with local GC content, but not recombination rate.

9 sure favoring the modification of the female recombination rate.

10 lleles and provides a high-resolution map of recombination rate.

11 eps and examine these dips in the context of recombination rate.

12 ontributions of intervalley processes in the recombination rate.

13 e/absence of variation with gene density and recombination rate.

14 fied associations with empirical measures of recombination rate.

15 he expression level of genes, as well as the recombination rate.

16 ross homologs has a strong impact on meiotic recombination rate.

17 in Morgans) controls for variability in the recombination rate.

18 introgression are predicted by variation in recombination rate.

19 been proposed to influence the variation in recombination rate.

20 regions with low methylation levels and high recombination rates.

21 genetic architecture of individual autosomal recombination rates.

22 on longer chromosomes, consistent with lower recombination rates.

23 nt shift in population size and/or effective recombination rates.

24 understand and utilize variation in meiotic recombination rates.

25 and that local gene-conversion rates reflect recombination rates.

26 accuracy than admixture-based estimation of recombination rates.

27 genes had lower promoter diversity and local recombination rates.

28 r how diffusion and coupling barriers affect recombination rates.

29 duce oxidant levels due to higher OH radical recombination rates.

30 LD information are unlikely to have elevated recombination rates.

31 tionally high mating frequencies and genomic recombination rates.

32 ing segments of identity by descent to infer recombination rates.

33 l of the photo-generated electrons with high recombination rates.

34 scriptional control elements affect germline recombination rates.

35 iting in founder animals, and low homologous recombination rates.

36 centrated to <5kb regions of highly elevated recombination rates (10-100x the background rate) called

37 th a characteristically high radical-radical recombination rate (2kdim = (1.3 +/- 0.1) x 10(9) M(-1)

38 metrics, linkage disequilibrium statistics, recombination rates, a battery of neutrality tests, and

39 is issue of GENETICS quantifies variation in recombination rate across a small region of the Drosophi

40 ise nucleotide diversity and divergence with recombination rate across the 20kb intervals, nor any ef

41 ference between subpopulations and increased recombination rates across pericentromeric regions.

42 nd PRDM9 function contribute to variation in recombination rates across the domestic horse genome.

43 The variation in local recombination rates across the Drosophila genome provide

44 otide diversity, linkage disequilibrium, and recombination rates across the genome.

45 Is the observed within-species variation in recombination rate adaptive?

46 ity with other grass genomes correlates with recombination rates along chromosomes.

47 map of SSCX to provide precise estimates of recombination rates along this chromosome and creating a

48 The apparent similarity of the variance in recombination rate among individuals between distantly r

49 By quantifying recombination rate and admixture proportions, we then sh

50 Remarkably, MAE genes exhibit an elevated recombination rate and an increased density of hypermuta

51 e current data on intraspecific variation in recombination rate and discuss the molecular and evoluti

52 , questioning whether an association between recombination rate and divergence between species has be

53 We study the relationship between recombination rate and gene regulatory domains, defined

54 o a genome-wide negative correlation between recombination rate and genetic differentiation among pop

55 h requires the implicit assumption that both recombination rate and genetic information are uniformly

56 eral explanation for the correlation between recombination rate and genetic variation.

57 A correlation between recombination rate and intraspecific diversity is in par

58 gnificant positive correlation between local recombination rate and local DNM rate, and that DNM rate

59 sence of a similar association between local recombination rate and nucleotide divergence between spe

60 has been a strong association between local recombination rate and nucleotide polymorphisms across t

61 The recombination rate and parental allele frequencies in ou

62 Furthermore, recombination rate and recombination hotspots have littl

63 ether the variation in N(e) is correlated to recombination rate and the density of selected sites in

64 Positive correlation between local recombination rate and the level of nucleotide polymorph

65 methods for inferring parameters such as the recombination rate and the selection coefficient have ge

66 s in the channel, effectively reducing their recombination rate and thus enhancing the performance fo

67 al part of the known correlation between the recombination rate and variant distribution appears to b

68 ies by examining the correlation between the recombination rate and variant landscape within the cont

69 s, levels of pre-existing genetic variation, recombination rates and adaptive landscapes.

70 of malaria, Plasmodium falciparum, the high recombination rates and associated vast diversity of its

71 cal genomic and epigenomic features, such as recombination rates and chromatin dynamics reshaped by i

72 in certain scenarios, such as unsatisfactory recombination rates and deleterious effects on physiolog

73 the two sexes, with the large difference in recombination rates and distributions able to be entirel

74 es of synonymous substitutions, we determine recombination rates and diversity levels of the shared g

75 ation, Newick tree output, variable mutation/recombination rates and gene conversion, and efficiently

76 an effect of local genomic features, such as recombination rates and gene densities that reshaped the

77 k Death, obtaining measurements of bacterial recombination rates and gene pool diversity of earlier e

78 the domestic horse, we calculated population recombination rates and identified likely recombination

79 The additive decreased carrier recombination rates and improved carrier mobility, both

80 in, increased gene density, elevated meiotic recombination rates and in the proximity of repetitive e

81 bining a tuneable energy gap, fast radiative recombination rates and luminescence quantum efficiencie

82 d sites has influenced the relations between recombination rates and patterns of molecular variation

83 c fields to perturb spin precession and thus recombination rates and photoreaction yields, giving ris

84 nt correlations between differences in local recombination rates and population differentiation quant

85 e that loss of NMD results in an increase in recombination rates and resistance to the DNA damaging a

86 mechanisms - especially considering variable recombination rates and ubiquitous background selection

87 ich allows us to estimate the spin-dependent recombination rate, and draw parallels with the Majorana

88 ytogenes we have detected differences in the recombination rate, and interestingly also divergence in

89 with suppressed re-absorption, reduced Auger recombination rate, and tunable Stokes shift is presente

90 colonies, assuming different mating numbers, recombination rates, and genetic architectures, to asses

91 genomic features (e.g., non-B DNA structure, recombination rates, and histone modifications) in +/-32

92 g imputing missing sequence data, estimating recombination rates, and inferring human colonization hi

93 requently binds promoters, despite their low recombination rates, and it can activate expression of a

94 genome, their preservation in areas with low recombination rates, and their preponderance in highly e

95 to their high color purity, low nonradiative recombination rates, and tunable bandgap.

96 short-circuit current, open-circuit voltage, recombination rates, and variations of the difference be

97 al populations, (2) at the 200-400 kb scale, recombination rate appears to vary largely genome-wide,

98 Nevertheless, DNA methylation and recombination rate are anticorrelated in all three speci

99 reeds showed that haplotypes associated with recombination rates are both old and globally distribute

100 s, which is in contrast with P. patens where recombination rates are evenly distributed along the chr

101 Furthermore, recombination rates are greatest in the middle of the ch

102 nd uniform recombination rate, especially if recombination rates are higher towards chromosome ends.

103 Here, we report that recombination rates are more than three orders of magnit

104 ficantly across the genome, and estimates of recombination rates are needed for downstream analyses s

105 However, many recent studies show that recombination rates are often very different even in clo

106 Recombination rates are reportedly high between these su

107 enteroviruses is associated with cVDPV, the recombination rates are similar for Sabin isolate-Sabin

108 d-state dynamics, with significantly reduced recombination rates as compared to conjugated dimers wit

109 ers such as the (scaled) population size and recombination rate, as well as many aspects of the recom

110 related with local genomic variables such as recombination rate, as well as with signals of recent po

111 this region in the genome, enhanced meiotic recombination rates, as well as other as-of-yet undefine

112 The variation of recombination rate at both fine and large scales cannot

113 ore quantify the effects of heterogeneity in recombination rate at broad and fine-scale levels on the

114 Additionally, the charge recombination rate at the p-GaInP2/TiO2 interface is gre

115 rsion loci relative to the true contemporary recombination rates at the loci but that recombination h

116 onstructing high-resolution maps of relative recombination rates based on the observation of ancestry

117 ue to (i) the reduction in the electron-hole recombination rate because of the reduced dimensions of

118 here is substantial variation in genome-wide recombination rate between individuals of both A. mellif

119 available for genetic markers, estimates of recombination rate between loci can be combined with LD

120 inc finger DNA binding explains variation in recombination rate between species.

121 There are also significant differences in recombination rate between subspecies of honeybee.

122 ntified both global and local differences in recombination rate between these two closely related spe

123 Using only regions with conserved recombination rates between and within species and accou

124 ynonymous/synonymous substitution rates, and recombination rates between HSV-1 glycoproteins and thei

125 es evidence of fine-scale differentiation in recombination rates between populations.

126 ~7.2-cM interval in a region with a moderate recombination rate but outside the least-recombining, pu

127 l, the point estimation of the corresponding recombination rate by population genetic methods tends t

128 level process can significantly increase the recombination rate (by three orders of magnitude) in agr

129 hin and among dyads, modifiers of the female recombination rate can function as potent suppressors or

130 ctors such as a small population size or low recombination rate can limit the action of natural selec

131 rmation at these sites, genetic modifiers of recombination rates can allow for meiotic progression.

132 ding efforts in crops; therefore, increasing recombination rates can reduce linkage drag and generate

133 Meiotic recombination rates can vary widely across genomes, with

134 cts the argument that the exceptionally high recombination rates cause a quantitative increase in off

135 nation rate valley" of significantly reduced recombination rate compared to matched control regions.

136 ion performance against advantages of higher recombination rate conferred by intron length.

137 This in turn reduces the electron/iodine recombination rate constant, which increases the collect

138 e V(oc) hysteresis is not due to a change in recombination rate constant.

139 ted that the theory of the MIF involves four recombination rate constants and an equilibrium constant

140 The relative amplitudes and first-order recombination rate constants of P(f) (0.4-0.6; 40-50 s(-

141 Bimolecular and Auger charge-carrier recombination rate constants strongly correlate with the

142 ed to extract the singlet and triplet charge recombination rate constants, k(CRS) and k(CRT), respect

143 A new study demonstrates that recombination rate divergence in two natural populations

144 Genomic recombination rate does not affect intra- and inter-colo

145 In general, local (fine-scale) variation in recombination rate, e.g. hotspots, has a small influence

146 omosome with the same map length and uniform recombination rate, especially if recombination rates ar

147 We find that recombination rates estimated by LDhat are biased downwa

148 the average proportion of admixture and the recombination rate estimates from the source populations

149 ionally, our method is able to produce local recombination rate estimates.

150 Existing methods for recombination rate estimation are limited by insufficien

151 cent years have seen progress in quantifying recombination rate evolution across multiple temporal an

152 mbination patterns and informing how quickly recombination rates evolve, how changes in recombination

153 When the recombination rate evolves, the conditions favoring asym

154 s, there is a trend for increased homologous recombination rates, except for the hybrids from one lin

155 When recombination rate fluctuations are included, there is a

156 pulation genetic estimate of the within-host recombination rate for HCV (0.28 x 10-7 recombination/si

157 MHz, k(T,s) = (43.97 +/- 0.01) MHz, and the recombination rate for singlet polaron pair k(S,r) = (88

158 ed population genetics methods for inferring recombination rates, for detecting selection, and for co

159 he existing procedures of estimating meiotic recombination rates from population genetic data.

160 modeling approach to infer substitution and recombination rates from whole-genome sequences and info

161 her genomic features (promoter polymorphism, recombination rate, gene length, and gene density) are a

162 ic filters, including filters for selection, recombination rate, genetic distance to the nearest gene

163 the field of photocatalysis, the high-charge recombination rate has been the big challenge to photoca

164 ing that the local departures from sex-equal recombination rates have evolved.

165 d "hotspots." Drosophila exhibit substantial recombination rate heterogeneity across their genome, bu

166 xplained 26.2% of the heritable variation in recombination rate in both sexes.

167 is locus has been previously associated with recombination rate in cattle.

168 9/SIX6OS1 was identified that influences the recombination rate in humans.

169 , nor any effect of maternal age in weeks on recombination rate in our sample.

170 gates can provide a pathway to slow down the recombination rate in photoelectrodes that utilize donor

171 local gene evolution correlate with the high recombination rate in the 2.8-Mb region with nine-fold h

172 Of interest, the female recombination rate in the 22q11.2 region was about 1.6-1

173 Enhancement of the radiative recombination rate in the presence of Ag-NPs induced LSP

174 light intensities due to a 40% faster charge recombination rate in the S(3) state.

175 For comparison, we measured recombination rates in a second population of male P. le

176 out population sizes, natural selection, and recombination rates in ancestral species from applicatio

177 To study the evolution of recombination rates in apes, we developed methodology to

178 pecific scale parameters that allow variable recombination rates in different populations.

179 be one mechanism that contributes to higher recombination rates in honeybees.

180 ubstantially disrupt the factors controlling recombination rates in humans.

181 fluorescent cytology to quantify genome-wide recombination rates in males from a wild population of t

182 arrier harvesting efficiencies and increased recombination rates in organic electronic devices.

183 The charge separation and recombination rates in PbS-MB(+) complexes were found to

184 ative explanations for the evolution of high recombination rates in social insects are therefore need

185 of the evolution of multiple mating and high recombination rates in social insects but our results al

186 Regions with elevated recombination rates in the entire cohort were enriched f

187 ds at meiosis I; detect selection for higher recombination rates in the female germ line by the elimi

188 hole transfer rate to the sum of the native recombination rates in the QD.

189 Determination of the inherent recombination rates in the quantum well confirms efficie

190 -based maps have the advantage of estimating recombination rates in the recent past rather than the d

191 Different recombination rates in various DNA regions (recombinatio

192 We confirm that the recombination rate increases with maternal age, while ho

193 Mutation and recombination rates independently associate with nucleot

194 substitutions and positively correlated with recombination rate, indicating widespread linked selecti

195 formed simulations to assess the accuracy of recombination rate inference in the presence of phase er

196 g imputing missing sequence data, estimating recombination rates, inferring human colonization histor

197 On average, the recombination rate is about 25-45% faster with respect t

198 The population-scaled recombination rate is approximately one-third of the mut

199 When the recombination rate is constant, Kelly's [Formula: see te

200 e proportion of interindividual variation in recombination rate is heritable, which indicates the pre

201 Understanding the causes of variation in recombination rate is important in interpreting and pred

202 However, the recombination rate is known to vary substantially along

203 er, is not extensive, and therefore, the low recombination rate is likely not a major constraint to a

204 ted gene loci (gene-specific sweeps), or the recombination rate is low without interfering genome-wid

205 ithin a 280 kb window, in which the maternal recombination rate is lower than the paternal one.

206 In contrast to the SDR, the maternal PAR recombination rate is much higher than the rates of the

207 Recombination rate is non-uniformly distributed across t

208 widespread pattern of sex differences in the recombination rate is not well understood and has receiv

209 d time scale in MAPbI3/Spiro-OMeTAD, and its recombination rate is similar to that in neat MAPbI3.

210 al theory calculations in which polaron pair recombination rate is suppressed by resonant exchange in

211 xis or automixis with central fusion and low recombination rates is inferred to be the cytogenetic me

212 enomena, we have a poor understanding of how recombination rate itself varies and evolves within a sp

213 impact of large tandem repeat arrays on the recombination rate landscape in an avian speciation mode

214 ences between individuals in the genome-wide recombination rate, levels of variation were low-within

215 However, the high electron-hole recombination rate limits the yield of highly oxidizing

216 In this study, we constructed fine-scale recombination rate maps for a natural population of the

217 nowledge, the first genome-wide mutation and recombination rate maps for HCMV, we show that genomic d

218 vals, and (3) interpopulation differences in recombination rate may be the result of local adaptation

219 mplies that species with a sufficiently high recombination rate may lose Prdm9 yet remain fertile.

220 s that genomic instability due to changes in recombination rates may directly contribute to the rate

221 Identifying recombination rate modifiers is thus of both fundamental

222 With this ABC we infer recombination rate, mutation rate, and recombination tra

223 Irrespective of the profound differences in recombination rates observed between sub-lineages and li

224 loss of these cells implies a remarkably low recombination rate of photogenerated carriers.

225 the predictions of BSC theory regarding the recombination rate of quasiparticles.

226 t EARs partially underlie the curiously high recombination rate of short chromosomes.

227 e series of polymers, as well as the fastest recombination rate of the charge-separated (CS) species,

228 f the two populations exhibiting the highest recombination rates of 0.26-0.27 cM/Mb.

229 e low absorption cross-section and ultrafast recombination rates of photoexcited carriers.

230 double-strand breaks can increase homologous recombination rates of single- and double-stranded oligo

231 tum mechanical calculations, including Auger recombination rates, of the quantum-confined Stark effec

232 examined the effect of local GC content and recombination rate on individual variant subtypes and pe

233 xceptionally large (14-Mb) region with a low recombination rate on the X chromosome that appears to h

234 Due to relatively higher recombination rates on smaller chromosomes, larger chrom

235 results predict that rapidly evolving female recombination rates, particularly around centromeres, sh

236 Average recombination rates peak near starts of genes and fall o

237 henylene-based systems exhibit slower charge-recombination rates presumably due to reduced electronic

238 addition, long chromosomes, which have lower recombination rates, produce stronger barriers on averag

239 ication, which in vivo increased PSII charge recombination rates, producing singlet oxygen and subseq

240 Here, we performed a comprehensive study of recombination rate (rate of meiotic crossing over) in tw

241 ely manifested as differences in genome-wide recombination rate rather than remodeling of the local r

242 lutionarily conserved elements, and have low recombination rates, reflecting the effects of purifying

243 ns, but simulating longer regions and higher recombination rates remains challenging.

244 ing data, we estimated the population-scaled recombination rate (rho) and found it to be significantl

245 nce with its role as a modifier of the human recombination rate, SIX6OS1 is essential for the appropr

246 and various evolutionary processes, meiotic recombination rates sometimes vary within species or bet

247 according to the distinct components of the recombination rate, specifically the genetic and physica

248 f many materials: for example, electron-hole recombination rates strongly depend on the character of

249 so found that the number of loci, as well as recombination rates substantially affect ERD.

250 schii chromosomes positively correlates with recombination rates, suggested a cause, and showed that

251 local density of functional elements and the recombination rate, suggesting that the landscapes have

252 mpared to the human genetic map, broad-scale recombination rates tend to be conserved, but with excep

253 y greater on a chromosome with a non-uniform recombination rate than on a chromosome with the same ma

254 In humans, males have lower recombination rates than females over the majority of th

255 nduced enhancement of radiative free carrier recombination rates that lasts even after the removal of

256 Due to tight linkage disequilibrium and low recombination rates, the number of haplotypes observed i

257 long carrier lifetimes and low non-radiative recombination rates, the same physical properties that a

258 -enriched BACs and are characterized by high recombination rates, there are also gene-dense regions w

259 relative contributions of mating number and recombination rate to colony genetic diversity have neve

260 lymorphism data and genome-wide variation in recombination rate to jointly infer the strength and tim

261 For even moderate ratios of the recombination rate to the selection coefficient, the sim

262 from finding disease-risk loci, to inferring recombination rates, to mapping missing contigs in the h

263 itative measurement of charge separation and recombination rates using state of the art computational

264 Our results suggest the existence of a recombination rate valley at regulatory domains and prov

265 This recombination rate valley is most pronounced for gene re

266 Each link type shows a "recombination rate valley" of significantly reduced reco

267 Recombination rate valleys show increased DNA methylatio

268 We investigated recombination rate variation in a large intraspecific hy

269 suggesting a common genetic architecture of recombination rate variation in mammals.

270 tics are preferred when information on local recombination rate variation is available.

271 Our study suggests that recombination rate variation is conserved at broad scale

272 ee text] statistics are more successful when recombination rate variation is controlled for.

273 Local and genome-wide recombination rate variation is shaping patterns of intr

274 terns and revealed how local and genome-wide recombination rate variation shapes patterns of introgre

275 important concepts such as recombination and recombination rate variation, genome sequencing, and seq

276 ding a human-realistic demographic model and recombination rate variation.

277 cial insects and the genetic architecture of recombination rate variation.

278 Recombination rates varied between subgenomes, with the

279 el systems, there remains little data on how recombination rate varies at the individual level in nat

280 Recombination rates vary between species and individuals

281 Meiotic recombination rates vary considerably between species, p

282 Recombination rates vary significantly across the genome

283 ation and offspring diversification, meiotic recombination rates vary within and between species.

284 hromosome was 84.61 cM; although the average recombination rate was 0.60 cM/Mb, both cold and hot rec

285 l distances was examined and the genome-wide recombination rate was found to be much smaller than mos

286 The heritability of autosomal recombination rate was low but significant in both sexes

287 g recombination dynamics to distributions of recombination rates, we identified populations of charge

288 other advantage, the electron back transfer (recombination) rates were slower with Cu((II/I))(tmby)2T

289 ature is confounded by wide variation in the recombination rate which has a complex relationship with

290 broad correlation between introgression and recombination rate, which determines the extent to which

291 Loci involved in recombination rate, which is an interesting trait for pl

292 the recovery of the ground state via charge recombination rates, which differ by up to 2 orders of m

293 c islands in general, have exceptionally low recombination rates, which may play a role in their esta

294 We also find a significant increase in recombination rate with distance from the centromere, mi

295 on in germ cells, we are able to predict the recombination rate with high accuracy.

296 rther increased by suppressing the radiative recombination rate with the introduction of an hBN space

297 Interestingly, variation in recombination rate within and between populations largel

298 ific genomic rearrangements and variation in recombination rate within the Z chromosome.

299 Nevertheless, the level of variation in recombination rate within wild populations-a key determi

300 virus polymerase, mutation of which reduces recombination rates without altering replication fidelit