ライフサイエンスコーパス: genetic map

1 rmative datasets (e.g. physical, optical and genetic maps).

2 4, on the reference 'TM-1' x 'Pima 3-79' RIL genetic map.

3 for expected linkage disequilibrium using a genetic map.

4 d BAC-to-BAC sequences and a high-resolution genetic map.

5 ated the genomic contigs with a high-density genetic map.

6 at genome assembly (cv. Svevo), and the DArT genetic map.

7 to the lack of marker density of the entire genetic map.

8 rganized around a physical map anchored to a genetic map.

9 f IBD segment endpoints and a pedigree-based genetic map.

10 enced 192 segregants to generate an accurate genetic map.

11 which were in good agreement with the NCCCWA genetic map.

12 y size and positively with the length of the genetic map.

13 d anchored the latter to chromosomes using a genetic map.

14 al-time sequencing, Hi-C, and a high-density genetic map.

15 ariation in baboons, as well as a fine-scale genetic map.

16 gle-molecule reads integrated to genomic and genetic maps.

17 AC)-end sequences and genotype-by-sequencing genetic maps.

18 l for comparing BAC-based physical maps with genetic maps.

19 uickly improve marker order and placement on genetic maps.

20 and as a resource to produce high-resolution genetic maps.

21 de CRM was constructed from 28 public cotton genetic maps.

22 ination with optical, chromosome-contact and genetic maps.

23 localizing these effects on high-resolution genetic maps.

24 ocessing and quantitative analysis and their genetic mapping.

25 vels in S. latifolia PAR genes identified by genetic mapping.

26 contain a translocation when analyzed using genetic mapping.

27 slocations: pollen viability and genome-wide genetic mapping.

28 er by as much as 180 degrees on the circular genetic map, a distance of >/=2 million base pairs.

29 Comparative genetic mapping also suggests that, at least in the case

30 Further, conditional genetic mapping analysis for GYD given its three compone

31 Here we report a combined sequence and genetic mapping analysis in outbred rats that maps 355 q

32 Strategically selected markers from the genetic map and draft genome assembly were employed to s

33 The genetic map and SSLP marker database constitute an essen

34 The assembly was anchored to a 992-locus genetic map and was annotated by comparison with >1.3 mi

35 A combination of genetic mapping and candidate gene analysis presents Cdk

36 in the pen1-1 genetic background as well as genetic mapping and characterization of the Arabidopsis

37 The genetic mapping and chromosome substitution line-based d

38 intervals predicted to be centromeric DNA by genetic mapping and DNA sequence analyses.

39 Genetic mapping and exome resequencing of individuals ac

40 genome-wide association study combined with genetic mapping and functional analysis identified a gen

41 Genetic mapping and gene expression analyses localized t

42 Despite years of research involving genetic mapping and gene expression profile analysis of

43 transmitted dominantly to her offspring, and genetic mapping and genome sequencing revealed a new mut

44 the development of powerful populations for genetic mapping and genome-wide association studies (GWA

45 By genetic mapping and in vitro analysis of enzyme activity

46 In particular, the problem of genetic mapping and linkage-one of the first efforts tow

47 Together, our results from genetic mapping and molecular analysis provide an exampl

48 A combination of sequence analysis, genetic mapping and molecular cytogenetic methods with c

49 We used genetic mapping and near isogenic lines (NILs) to identi

50 Genetic mapping and phylogenetic analysis indicate that

51 se gene silencing, gene expression analysis, genetic mapping and population genomics to study the gen

52 Through genetic mapping and positional cloning, we identified th

53 in the suppressor mutants were identified by genetic mapping and re-sequencing of the mutant genomes.

54 A combination of genetic mapping and retroillumination photography was us

55 Genetic mapping and sequencing of mutant alleles confirm

56 mal recessive syndrome of neonatal diabetes, genetic mapping and subsequent sequencing identified mut

57 ure of human diseases governs the success of genetic mapping and the future of personalized medicine.

58 Genetic mapping and viral-induced gene silencing were us

59 ased experimental data, involving systematic genetic mapping and whole-genome sequencing, to generate

60 New markers, genetic maps and extensively curated qualitative/Mendeli

61 h large-scale cDNA analyses, construction of genetic maps and gene mapping studies aiming to link phe

62 Significantly more quantitative trait loci, genetic maps and markers are available in MapViewer, a n

63 lity of SLAF markers for rapid generation of genetic maps and QTL analysis has been demonstrated for

64 The comparison between genetic maps and the reference genome highlighted 85% of

65 finium SNP array, constructed a 7,185-marker genetic map, and anchored on the map contigs totaling 4.

66 tudy we combined next-generation sequencing, genetic mapping, and a set of physiological traits of th

67 e-molecule real-time sequencing, optical and genetic mapping, and an assembly reconciliation algorith

68 avioral and anatomical analyses, physiology, genetic mapping, and gene knockdowns.

69 r the array, 4.5% were markers from existing genetic maps, and 61% were selected based on distributio

70 and expressed sequence tag (EST) sequences, genetic maps, and transcriptome profiles for cucurbit sp

71 More generally, our genetic mapping approach should be powerful for high-res

72 We apply a powerful genetic mapping approach to the Wellcome Trust Case-Cont

73 tive genome structure analysis and classical genetic mapping approaches feasible.

74 However, as in conventional genetic mapping approaches, mapping-by-sequencing requir

75 Using a combination of genetic mapping approaches, we show that the white reces

76 transcriptional profile and combined it with genetic mapping approaches.

77 Wheat (Triticum aestivum) genetic maps are a key enabling tool for genetic studies

78 Genetic maps are key tools in genetic research as they c

79 ifers have recently been produced, but dense genetic maps are needed to comprehend genome macrostruct

80 grate sequence information with physical and genetic maps are scarce.

81 Accurate genetic maps are the cornerstones of genetic discovery,

82 Genetic maps are the foundation for anchoring and orient

83 d displayed a nonuniform distribution on the genetic map around the donor r1-sc:m3 locus.

84 Genetic mapping associated a large deletion on chromosom

85 on of a single-nucleotide polymorphism-based genetic map at the F4 stage of the mapping population.

86 00 meioses and have constructed sex-specific genetic maps at a previously unachievable resolution.

87 Compared to the human genetic map, broad-scale recombination rates tend to be

88 ap between markers D3Mit147 and D3Mit19 on a genetic map, but the physical map places RPE65 outside t

89 Genetic mapping by bulk segregation analysis excluded al

90 Here we present a statistical framework for genetic mapping by utilizing collective information in b

91 Here, we argue that genetic mapping can play a more important role in studyi

92 Most of the published cotton genetic maps can be viewed and compared using CMap, a co

93 Genetic maps can provide essential knowledge for underst

94 g the gap between large-scale and fine-scale genetic mapping, can reveal new features of the recombin

95 riation (PAV) markers were used to develop a genetic map comprising 40 linkage groups, the first repo

96 Conventional genetic mapping confirmed that the causal mutations were

97 SSLPs were genotyped, yielding a 2886-marker genetic map consisting of 10 major linkage groups betwee

98 Consensus genetic maps constructed from multiple populations are a

99 approach was used to develop SNP markers for genetic map construction, and quantitative trait loci (Q

100 ental RIL populations to produce a consensus genetic map containing 37 372 SNPs.

101 ibrium methodology to generate an integrated genetic map containing 4,817 SNPs, which spanned a total

102 bled the construction of two high-resolution genetic maps containing 1832 and 1773 markers with an av

103 The final genetic map contains 7,192 successfully mapped markers t

104 Here, we use genetic mapping, copy-number analysis, exclusion of muta

105 We applied this model to analyze genetic mapping data from the OP design of a gymnosperm

106 e code development, gene number proposition, genetic mapping, data banks, gene-disease maps, catalogs

107 ParentChecker efficiently improves genetic mapping datasets for cases where parental inform

108 Here, we describe a combined physical and genetic map derived from a cross between the drug-type s

109 Using a scarcely dense genetic map derived from a population of 134 individuals

110 The genetic map derived from this population provided no ind

111 rphisms (SNPs) have become popular tools for genetic mapping, discovery and application of SNPs in po

112 easure and susceptible to confounding during genetic mapping due to correlation with flowering and su

113 This genetic map enabled the anchoring of 100 Mb of WGS and 4

114 This first genetic map enables us to study the goldfish genome evol

115 holds great promise to extend the utility of genetic mapping, even when QTL effects are modest or com

116 sis, de novo genome assembly and annotation, genetic mapping, exome resequencing of natural populatio

117 onal phenomenon that we observed through our genetic mapping experiments was that the T-DNA junctions

118 To underpin construction of a genetic map facilitating isolation of these S locus gene

119 We performed genetic mapping, followed by next-generation sequencing

120 In this study, a high-density genetic map for cultivated cucumber was developed that c

121 We constructed a genetic map for the Z chromosome of the Gouldian finch (

122 We present a genetic map for Xenopus tropicalis, consisting of 2886 S

123 are fewer tools available which can display genetic maps for less well-characterized species, and in

124 order 10 Mb) features of previously reported genetic maps for mouse.

125 se high-density maps are the first available genetic maps for seashore paspalum.

126 estimate and test these parameters within a genetic mapping framework using a new powerful computati

127 orporating integrated square errors into the genetic mapping framework.

128 eloped methodology to construct a fine-scale genetic map from high-throughput sequence data from 10 W

129 ide polymorphisms (SNPs) were identified for genetic mapping from rp2 P450s and other genes revealing

130 e that encodes PRDM9, we inferred fine-scale genetic maps from population resequencing data for two b

131 We use a combination of genetic mapping, gene expression analyses, and functiona

132 d sequence tags (ESTs), markers, trait loci, genetic maps, genes, taxonomy, germplasm, publications a

133 massively parallel sequencing technologies, genetic mapping has become the rate limiting step in mam

134 ailability of whole-genome sequencing (WGS), genetic mapping has become the rate-limiting step, inhib

135 Genetic mapping has been used as a tool to study the gen

136 Although genetic maps have been developed for numerous plant spec

137 s of interest: haplotype-based computational genetic mapping (HBCGM).

138 Genetic mapping identified a genomic locus containing th

139 Genetic mapping identified the candidate gene linking AH

140 Genetic mapping identifies strain line 19 fusion (F) pro

141 tio of the linkage disequilibrium map to the genetic map in Morgans) controls for variability in the

142 Using genetic mapping in cichlid fishes, we identified shared

143 , we performed sequenced-based, high-density genetic mapping in F2 hybrids between synthetic and natu

144 We use genetic mapping in large F(2) intercrosses between Gough

145 resent MULTIPOOL, a computational method for genetic mapping in model organism crosses that are analy

146 Genetic mapping in this population, derived from a cross

147 oach that localizes causal variants based on genetic maps in linkage disequilibrium units (LDU maps).

148 -seq was performed to construct high-density genetic maps in two seed families.

149 folds using Illumina mate-pair libraries and genetic map information.

150 ure, CloudMap allows users to sharply define genetic map intervals graphically and to retrieve very s

151 e clustering and network reconstruction with genetic mapping into a unifying framework.

152 Resolution of genetic mapping is limited by the recombination rate.

153 Further genetic mapping is warranted at these loci.

154 Total genetic map length and local recombination landscapes ty

155 figl1 mutations, which increased the hybrid genetic map length from 389 to 3,037 cM.

156 ombining pseudo-autosomal region (PAR) whose genetic map length is approximately 25 cM in both male a

157 he effect of variant density, conditional on genetic map length, on the power to resolve IBD segments

158 A combination of genetic mapping, linkage group selection, and functional

159 nd summarize patterns of TRD from across the genetic mapping literature.

160 Refined genetic mapping localizes vitiligo risk in the HLA-A reg

161 ymorpha research by linking the physical and genetic maps, making novel genomic and genetic analyses,

162 European ancestry in the Americas to build a genetic map measuring the probability of crossing over a

163 icitly incorporate their LD information into genetic mapping models (tmLD).

164 After genetic mapping, mutations in three known LD regulatory

165 A high-density genetic map of a B. graminis family segregating for Pm1a

166 Taking advantage of the ultra-high-density genetic map of a population of 210 recombinant inbred li

167 cent genomic studies have provided a refined genetic map of acute lymphoblastic leukemia (ALL) and in

168 We have defined a high-resolution genetic map of direct interference by Cascade and Cas3,

169 Our project has patched the hole in the genetic map of Eurasia: we demonstrated complexity of ge

170 Therefore, we have developed a dense genetic map of M. fusca using tunable genotyping-by-sequ

171 ime of development, which provides the first genetic map of neurogenesis in a cephalopod.

172 A consensus genetic map of tetraploid cotton was constructed using s

173 The resulting sex-averaged genetic map of the DO population is highly concordant wi

174 We created a genetic map of the sex chromosome and its homeologs in F

175 are very limited partly due to the lack of a genetic map of this interesting wild apple.

176 A high-resolution genetic map of this region delineated the location of ui

177 e reference genome sequence was validated by genetic mapping of 54,000 SNPs, and annotated with 26,66

178 Here we report genetic mapping of a membrane transporter (ABCC2) to a l

179 Using genetic mapping of a strong cutin-deficient mutation, we

180 Here we report discovery and genetic mapping of additional vibrator modifiers, Mvb2 a

181 Genetic mapping of affected individuals resulted in the

182 in these half-tetrad individuals allowed the genetic mapping of all 19 centromeres of the Brassica A

183 od 1950-1970, groundbreaking research on the genetic mapping of Chlamydomonas reinhardtii and the use

184 Genetic mapping of complex diseases to date depends on v

185 Together, these results make clear that genetic mapping of complex phenotypes is within reach, e

186 f genome-wide association studies (GWAS) for genetic mapping of complex traits, most existing GWAS me

187 Through genetic mapping of disease loci and whole-exome sequenci

188 In support of this, genetic mapping of DNA methylation reveals that most of

189 Genetic mapping of impulsive action in the BXD panel ide

190 Using forward-genetic mapping of inceptin-induced plant responses, we

191 ration of these various data sets enable the genetic mapping of many new phenotypes and facilitates t

192 t these hypotheses by performing large-scale genetic mapping of mating behavior using hybrids of two

193 e analysis was the primary tool used for the genetic mapping of Mendelian and complex traits with fam

194 Genetic mapping of mutations in model systems has facili

195 Despite advances in genetic mapping of quantitative traits and in phylogenet

196 Genetic mapping of resistance mutation coupled with pote

197 characterized in Drosophila melanogaster by genetic mapping of resistance to the cyclodiene dieldrin

198 e physical maps were validated with FISH and genetic mapping of SNP markers derived from BES.

199 ses, this result is consistent with previous genetic mapping of teratoma susceptibility loci to the r

200 al data, we used codominant genic markers in genetic mapping of the dioecious plant Silene latifolia,

201 Recent genetic mapping of the molecular evolution of pancreatic

202 The target link to GyrB was confirmed by genetic mapping of the mutations conferring resistance t

203 High resolution genetic mapping of transcript levels in HMDP, reveals bo

204 tic basis for differential responses through genetic mapping of V2O5-induced lung collagen content in

205 Similar genetic mapping of Wilms' tumor-1-positive mesothelial c

206 Here, we report genetic mapping of XLCOD to Xq26.1-qter.

207 These models provide comprehensive genetic maps of lineage-specific Notch receptor expressi

208 bined multiple data sets to build integrated genetic maps of the M. guttatus species complex (section

209 We constructed high-density genetic maps of Zoysia japonica using a restriction site

210 interactions between segments distant on the genetic map on contact frequencies determined experiment

211 Genetic mapping on fully sequenced individuals is transf

212 ction of rice flowering-time plasticity in a genetic mapping population grown in natural long-day fie

213 This question is best addressed in a genetic mapping population in which all molecular polymo

214 We used a genetic mapping population of wild tobacco, Nicotiana at

215 ctive incorporation of AMF-resistance into a genetic mapping population to evaluate maize response to

216 hat the F3'5'H gene cosegregates with b in a genetic mapping population, strongly support our hypothe

217 Genetic mapping populations have facilitated identificat

218 ish causal relationships among phenotypes in genetic mapping populations.

219 any commonly sought beneficial properties of genetic mapping populations.

220 ith a Genetic Algorithm to analyze data from genetic mapping populations.

221 tortion (TRD)] are also commonly observed in genetic mapping populations.

222 Molecular genetic mapping positioned the turnout mutation within a

223 and corresponded well to previously reported genetic map positions.

224 We developed a next-generation computational genetic mapping program with advanced features to identi

225 This high-density genetic map provides a genomic resource and practical to

226 Comparative genetic mapping provides insights into the evolution of

227 nted the most promising candidate traits for genetic mapping related to BP based on strong heritabili

228 Statistical methods for genetic mapping rely on a key assumption, that is, trait

229 pressures, high diversity and precision for genetic mapping remain.

230 Genetic mapping restricted to genome-wide enhancer singl

231 We report genetic mapping results in laboratory-raised families of

232 urthermore, our gene-expression analysis and genetic mapping results suggest that cis-regulatory chan

233 Genetic mapping revealed that a locus on chromosome 6 li

234 Genetic mapping revealed that the pe locus represents a

235 Genetic mapping revealed that the reduction in acylsugar

236 We conducted a systematic study including genetic mapping, sequencing, and functional analyses to

237 We used genetic mapping, sequencing, transgenic technology, CRIS

238 The physical and genetic map should facilitate further dissection of gene

239 Sequence analyses and genetic mapping show that the sex-linked regions of thes

240 Genetic mapping showed that phosphorylated LRP6 degradat

241 Through fine-scale genetic mapping, site-directed mutagenesis, and transgen

242 ts that are challenging to handle by current genetic mapping software with graphical interface.

243 In this study, we use a genetic mapping strategy that involves recurrent backcro

244 Evidence from human myopia genetic mapping studies (MYP3 locus), modulated animal m

245 RECENT FINDINGS: Computational genetic mapping studies have identified the genetic basi

246 Genetic mapping studies have suggested that diploid cott

247 eous and large enough to permit well-powered genetic mapping studies of quantitative traits relevant

248 Genetic mapping studies of quantitative traits typically

249 these "exchangeless" homologs has come from genetic mapping studies of trisomic conceptuses, so the

250 se mechanisms of NS are not well understood, genetic mapping studies suggest a multitude of unknown s

251 Genetic mapping studies suggest high genetic heterogenei

252 digrees offer many well-known advantages for genetic mapping studies, including cost-efficient study

253 Furthermore, in genetic mapping studies, Mx1 was identified as the major

254 the evidence for pleiotropy in contemporary genetic mapping studies, new and established analytical

255 teractions (HGIs) are difficult to detect in genetic mapping studies, therefore, few examples of them

256 In genetic mapping studies, we identify four additive modif

257 depth to achieve desired marker density for genetic mapping studies.

258 ategy can be broadly applied to other rodent genetic mapping studies.

259 diseases in humans, causal loci uncovered by genetic-mapping studies explain only a minority of the h

260 We performed a genetic mapping study using the Immunochip to determine

261 ial benefits of using population isolates in genetic mapping, such as reduced genetic, phenotypic and

262 Genetic mapping suggested important roles for variation

263 tations in the fly genome by combining rough genetic mapping, targeted DNA capture, and second genera

264 We used genetic maps that capture detailed linkage disequilibriu

265 In combination with the high-resolution genetic map, the draft genome paves the way for better m

266 Together with comparative genetic mapping, this has revealed that sex-determining

267 a novel statistical approach to comparative genetic mapping to detect large-scale structural mutatio

268 ckcross design, we performed high-resolution genetic mapping to determine the genetic architecture of

269 ressed at static and ontogenetic levels into genetic mapping to identify the quantitative trait loci

270 , but previous applications involved tedious genetic mapping to pinpoint the causative mutations.

271 its the profound differences in sex-specific genetic maps to classify pairs as maternally or paternal

272 and mediation techniques, we leverage these genetic maps to predict 213 causal relationships between

273 into virus-host interactions, all made using genetic mapping tools in mice.

274 outperforms three existing state-of-the-art genetic mapping tools.

275 RDN1 gene, Medtr5g089520, was identified by genetic mapping, transcript profiling, and phenotypic re

276 a five- to eight-fold higher resolution than genetic maps used in similar studies.

277 Our principal goal was to construct a genetic map using integrated approaches of genetic, comp

278 The constructed genetic map using the SFP markers predicted from our pro

279 report a fast and cost-effective method for genetic mapping using next-generation sequencing that co

280 Genetic mapping using SNP markers confirms its position

281 We describe analytical methods for genetic mapping using this resource and demonstrate the

282 comparing whole genome polymorphism data and genetic maps using a coalescent modeling framework, we e

283 Genetic mapping utilized patient samples from Germany (2

284 Quantitative genetic mapping utilizing crosses between D. tenebrosa a

285 A local genetic map was constructed by genotyping three flanking

286 A recombination bin-based genetic map was constructed, with 5,816 bins and 20 link

287 Genetic mapping was recently used to identify the underl

288 ning transcriptome, iTRAQ-based proteome and genetic mapping was taken to compare the ovules of the X

289 By anchoring the S. pennellii genome to the genetic map, we define candidate genes for stress tolera

290 cent developments in parallel computing, and genetic mapping, we derive, de novo, a sequence assembly

291 By genetic mapping, we identified a frame shift mutation in

292 whole genome SNP database and computational genetic mapping were used to analyze the murine genetic

293 Genetic maps were constructed following identical rules

294 terspecific Gossypium hirsutumxG. barbadense genetic maps were used for assembling a high density con

295 Historically, 'genetic maps' were used primarily to locate genes.

296 omes resulted in the de novo construction of genetic maps which were in good agreement with the NCCCW

297 A high level of synteny was found with pine genetic maps, which should facilitate the transfer of st

298 ility of a high-quality sequence anchored to genetic maps will accelerate the identification of genes

299 The genetic maps will assist in genome sequence assembly, ta

300 e diploid D genome and the tetraploid cotton genetic map, with only a few minor possible structural r