ライフサイエンスコーパス: inbred line

1 ntrogressed into a disease-susceptible maize inbred line.

2 sava and comparative analyses with a partial inbred line.

3 sing genetically modified substrains of this inbred line.

4 c background of cv. NC 84173, a fresh market inbred line.

5 numerous previously non-transformable maize inbred lines.

6 gene variants present in the many available inbred lines.

7 ompared with B73 and Tx601 maize susceptible inbred lines.

8 ed representation sequencing of 14,129 maize inbred lines.

9 scriptome-wide association studies using 505 inbred lines.

10 ata obtained by RT-qPCR technique from maize inbred lines.

11 other flavonols were identified in these two inbred lines.

12 of sequence variants among these widely used inbred lines.

13 netic Reference Panel (DGRP) of wild-derived inbred lines.

14 ion differences are inherited by recombinant inbred lines.

15 th 100% efficiency, allowing the creation of inbred lines.

16 panel of Drosophila melanogaster recombinant inbred lines.

17 in non-allelic positions in the two parental inbred lines.

18 nt inbred line families derived from diverse inbred lines.

19 s of having a large genome and lack of fully inbred lines.

20 ity of a large number of naturally occurring inbred lines.

21 a recessive, duplicate-factor trait in some inbred lines.

22 ormly leads to tolerance within standard MHC-inbred lines.

23 ation in populations generated from multiple inbred lines.

24 yellow1 (vey1) that varies between different inbred lines.

25 limited variations in their boundaries among inbred lines.

26 ified using eRD-GWAS on a panel of 369 maize inbred lines.

27 by crossing B73 and each of the three other inbred lines.

28 ssion (OE; B104 inbred) or knockout (KO; W22 inbred) lines.

29 genetic diversity in a diverse set of maize inbred lines; (2) determine the level of genetic diversi

30 advanced backcross (28.6 cM) and recombinant inbred line (32.3 cM) populations.

31 We also identify, in recombinant inbred lines, a locus that affects maternal hatching, a

32 Inbred lines A188 and B73 were cultivated under sufficie

33 The Lancaster Surecrop-derived inbred line A619 carries a restorer that is distinct fro

34 e and transcriptome variation in elite maize inbred lines across heterotic pools.

35 eyed how the genetic divergence of two maize inbred lines affects the transcriptomic landscape in fou

36 g with a new advanced intercross-recombinant inbred line (AI-RIL) population, we show that a QTL tigh

37 porter-modified Bay-0 x Shakdara recombinant inbred line and localized heritable variation.

38 identified in earlier studies with the same inbred lines and associated with biometrical, physiologi

39 ns, C57BL/6J and DBA/2J, several recombinant inbred lines and cerebellar mutant strains.

40 146 maize genotypes comprising of landraces, inbred lines and commercial hybrids.

41 equence polymorphisms among 27 diverse maize inbred lines and discovered that the genome was characte

42 es of several commonly used maize (Zea mays) inbred lines and has been anecdotally linked to enhanced

43 We show that inbred lines and hybrids differ consistently in the comp

44 as more common in landraces than in improved inbred lines and hybrids.

45 ragenotypic variability), we used Drosophila inbred lines and measured the spontaneous locomotor beha

46 mine the level of genetic diversity in INERA inbred lines and patterns of relationships of these inbr

47 enced North American Drosophila melanogaster inbred lines and present the first ever data set and ana

48 ints of floral transition of almost 30 maize inbred lines and show that tropical lines exhibit a dela

49 NILs derived from crosses between 18 diverse inbred lines and the recurrent inbred parent B73, referr

50 y comparing the microbiomes of diverse maize inbred lines and their F(1) hybrid offspring, which we q

51 ference persisted in hybrids and recombinant inbred lines and was mapped to a single expression quant

52 Comparisons between two inbreds lines and between ab- and adaxial anther florets

53 notypes, a mapping population of recombinant inbred lines, and a dense single-nucleotide polymorphism

54 They are particularly useful when inbred lines are available, because once these lines hav

55 Other inbred lines are known to transcribe significantly diffe

56 F1 progeny of such inbred lines are often more vigorous than their parents,

57 the sets of transcribed genes in additional inbred lines, arising from inbred-specific DNA methylati

58 e cultivars, such as the sequenced reference inbred line B73.

59 utagenized population derived from the maize inbred line B73.

60 ssues representing 11 major organ systems of inbred line B73.

61 n three copies of chromosome 10 derived from inbred lines B73 and H99.

62 ated how the genetic divergence of the maize inbred lines B73 and Mo17 and their F1 hybrid progeny is

63 criptomic divergence of the maize (Zea mays) inbred lines B73 and Mo17 and their reciprocal F1 hybrid

64 MM to DNA sequencing data from the two maize inbred lines B73 and Mo17 to identify CNVs that may play

65 me shotgun (WGS) sequences for the two maize inbred lines B73 and Mo17 using k-mer analysis to quanti

66 onmental conditions in hybrid progeny of the inbred lines B73 and Mo17.

67 g two whole-genome de novo assemblies of the inbred lines B73 and PH207.

68 how sRNA populations vary between two maize inbred lines (B73 and Mo17) and their hybrid.

69 analyses of the cuticular waxes of two maize inbred lines (B73 and Mo17), and their genetic hybrids,

70 ot and shoot tissues of two maize (Zea mays) inbred lines (B73 and Mo17).

71 de map of cytosine methylation for two maize inbred lines, B73 and Mo17.

72 ropagated tetraploid into a seed-propagated, inbred-line-based hybrid, but this process requires a be

73 y genome sequence is available for the elite inbred line BTx623, but functional validation of genes r

74 are not specific to the Col-Cvi recombinant inbred lines but have an epigenetic state that is inhere

75 ant of hybrid rice (derived from recombinant inbred lines) by comprehensively evaluating all possible

76 Previously genotyped accessions (natural inbred lines) can be grown in replicate under different

77 Only three maize inbred lines carrying the three-copy allele were identif

78 rmediate of transposition) in 98 recombinant inbred lines constructed from a line exhibiting high cop

79 hysiological comparison of maize recombinant inbred lines contrasting in RCA grown under suboptimal a

80 multiple interval mapping (MTMIM) of QTL for inbred line crosses.

81 i (QTL) for total fitness in 398 recombinant inbred lines derived from a cross between locally adapte

82 The DGRP consists of fully sequenced inbred lines derived from a natural population.

83 Recombinant inbred lines derived from Col and Cvi were used to exami

84 We produced 1,636 MAGIC maize recombinant inbred lines derived from eight genetically diverse foun

85 Twenty inbred lines derived from nature were measured for their

86 Inbred lines derived from T. mirus with a dominant d-rDN

87 A population of recombinant inbred lines derived from the tetraploid durum wheat var

88 r castaneus map, and a map constructed using inbred lines derived predominantly from M. m. domesticus

89 using an independent population of backcross inbred lines, derived from the same parents, which allow

90 RP) is a community resource of 205 sequenced inbred lines, derived to improve our understanding of th

91 rared imaging in a population of recombinant inbred lines developed from a cross between KS4895 and J

92 Recombinant inbred lines developed from the maize (Zea mays ssp. may

93 lines and patterns of relationships of these inbred lines developed from two sources; and (3) examine

94 leotide polymorphisms (SNPs) among surviving inbred lines deviated from neutral expectations.

95 Distantly related maize (Zea mays) inbred lines display an exceptional degree of genomic di

96 specific transcriptomes from two contrasting inbred lines during root growth.

97 hort-read sequence data from a single highly inbred line each from D. simulans, D. mauritiana, and D.

98 families composed of ~200 random recombinant inbred lines each from crosses between a common referenc

99 oss (CC) is a panel of eight-way recombinant inbred lines: eight diverse parental strains are interma

100 abidopsis accessions, epigenetic recombinant inbred lines (epiRILs) and also verified in rice.

101 idopsis population of epigenetic recombinant inbred lines (epiRILs) for resistance against Hyaloperon

102 1-2 (ddm1-2)-derived epigenetic recombinant inbred lines (epiRILs) in Arabidopsis thaliana is well s

103 rge panel of isogenic epigenetic recombinant inbred lines (epiRILs) to derive a recombination map bas

104 c contribution to heterosis using epigenetic inbred lines (epiRILs) with varying levels and distribut

105 ng at elevated levels in the scutella of all inbred lines examined, kauralexins appear ubiquitous in

106 Multi-parent crosses of recombinant inbred lines exist in many species for fine-scale analys

107 pping population, composed of 25 recombinant inbred line families derived from diverse inbred lines.

108 study was carried out to (i) assess a set of inbred lines for combining ability under stressed and op

109 We tested 92 SNP-genotyped inbred lines for yield component traits, N uptake effici

110 Arabidopsis thaliana epigenetic recombinant inbred lines found no evidence in support of any role fo

111 of DNA methylation in five maize (Zea mays) inbred lines found that while DNA methylation levels for

112 AM) population, comprising 4,998 recombinant inbred lines from 25 biparental families, and in an asso

113 soybean chromosome 13 using 184 recombinant inbred lines from a 'Wyandot' x PI 567324 cross.

114 We screened 593 inbred lines from an Arabidopsis multiparent advanced ge

115 very close to the centromere in recombinant inbred lines from an intermated B73 x Mo17 population, s

116 We derived inbred lines from ancestral and evolved populations and

117 Using a population of recombinant inbred lines from resistant and susceptible parents, the

118 was developed and applied to 741 recombinant inbred lines from six mapping populations.

119 A training population made up of 384 inbred lines from the Ames Panel was phenotyped by extra

120 -based genetic map by genotyping recombinant inbred lines from the intermated B73 x Mo17 population.

121 osynthesis in the flag leaves of recombinant inbred lines from wheat cultivars Seri M82 and Babax (SB

122 es, we genotyped an association panel of 508 inbred lines genotyped with a total of ~550,000 SNPs (Il

123 d 219 soybean accessions and 152 recombinant inbred lines genotyped with high-density markers and phe

124 Surprisingly, crickets from inbred lines had a greater encapsulation ability compare

125 eaf number at flowering in RILs (Recombinant Inbred Lines) harboring the SG allele.

126 Our results suggest that the large-egg inbred line has acquired compensating properties that co

127 c regions, which suggested that selection in inbred lines has been less efficient in these regions be

128 support the sequenced genomes of many maize inbred lines in addition to the B73 reference genome ass

129 The use of well-structured recombinant inbred lines in combination with "omics" analysis can he

130 to analyze the metabolomes of the 282 maize inbred lines in the Goodman Diversity Panel.

131 rom 368 diverse temperate and tropical maize inbred lines in this study.

132 as long been constrained by the lack of true inbred lines in zebrafish.

133 s demonstrated by characterizing recombinant inbred lines, including Oh43, which has a point mutation

134 Many maize inbred lines, including some adapted to tropical regions

135 he same pattern was observed in historically inbred lines, indicating a high frequency of recessive l

136 ulation with a limited number of recombinant inbred lines, it is unnecessary to genotype the lines wi

137 response, we present the Joint Genotyper for Inbred Lines (JGIL) as a method for obtaining genotypes

138 c data for more than 1,000 different natural inbred lines led to the development of several data repo

139 ight-week old male mice from two recombinant inbred lines (LGXSM-6 and LGXSM-33) were subjected to ax

140 These results suggest that, at least in inbred lines like those examined here, mutational pressu

141 relatively resistant to MD and from another inbred line (line 7(2)) that is highly susceptible to MD

142 lowering time with a set of 5000 recombinant inbred lines (maize Nested Association Mapping populatio

143 In the Arabidopsis multiparent recombinant inbred line mapping population, a limited number of plan

144 In a recombinant inbred line mapping population, copy number variation of

145 We previously showed that the maize inbred line Mp708, which was developed by classical plan

146 semblies for the complex genome of the maize inbred line NC358 using PacBio datasets ranging from 20

147 ve resistance in maize, we evaluated a 5,000-inbred-line nested association mapping population for re

148 In further comparisons of 60 diverse inbred lines, non-syntenic genes were six times more lik

149 ing effect of other viruses, we generated an inbred line of flies with galbut virus as the only detec

150 embryos from crosses between two polymorphic inbred lines of Arabidopsis thaliana and used single-nuc

151 urally dispersing populations of recombinant inbred lines of Arabidopsis thaliana segregating early a

152 this issue by exposing a set of recombinant inbred lines of Arabidopsis thaliana to a simulated glob

153 e method to data from a panel of recombinant inbred lines of Arabidopsis thaliana, descended from 19

154 llocation among floral whorls in recombinant inbred lines of Brassica rapa in multiple environments t

155 of reproduction over ontogeny in recombinant inbred lines of Brassica rapa in the field and glasshous

156 Using recombinant inbred lines of Brassica rapa, we examined the quantitat

157 In this study we determined that two inbred lines of chicken differing in their genetic backg

158 in Mozambique was compared among recombinant inbred lines of common bean (Phaseolus vulgaris) having

159 riptomic response to cold was studied in two inbred lines of contrasting cold-tolerance.

160 ion spanning the bab1 and bab2 genes from 94 inbred lines of D. melanogaster sampled from a single lo

161 tify phytosterols and triterpenes from seven inbred lines of Djulis hull using GC-MS.

162 tary perturbation on metabolic traits in 146 inbred lines of Drosophila melanogaster and show that ge

163 lar odorants in a population of wild-derived inbred lines of Drosophila melanogaster.

164 variation of defensin genes was examined in inbred lines of Leghorn and Fayoumi chickens, and a dupl

165 Each member of a collection of 231 diverse inbred lines of maize constituting a high-resolution ass

166 plant height data involving 3502 recombinant inbred lines of maize planted in multiple discrete envir

167 ned incubation time data from five different inbred lines of mice with quantitative gene expression p

168 is a genetic reference panel of recombinant inbred lines of mice, designed for the dissection of com

169 variation in cone photoreceptor number among inbred lines of mice, identifying candidate genes that m

170 We find analogous results in recombinant inbred lines of the Bayreuth x Shahdara cross, which dif

171 l coma recovery) in the unrelated, sequenced inbred lines of the Drosophila melanogaster Genetic Refe

172 s at 1, 2, and 4 wk of age in the sequenced, inbred lines of the Drosophila melanogaster Genetic Refe

173 ariation in gene expression in the sequenced inbred lines of the Drosophila melanogaster Genetic Refe

174 in 3 thermal environments for the sequenced, inbred lines of the Drosophila melanogaster Genetic Refe

175 sophila life history traits in the sequenced inbred lines of the Drosophila melanogaster Genetic Refe

176 a recovery time, in the unrelated, sequenced inbred lines of the Drosophila melanogaster Genetic Refe

177 ter stages of development in 197 recombinant inbred lines of two different maize (Zea mays) populatio

178 eate large numbers of mutant embryos without inbred lines opens exciting new possibilities for studyi

179 hybrids to a control population selected on inbred line performance when the number of quantitative

180 hen introgressed by backcross into the maize inbred line PH09B, the mutant phenotype of vyl lasted mu

181 we generated a draft genome assembly of the inbred line PH207 to complement and compare with the exi

182 f samples in a subtropical maize recombinant inbred line population (CML444 x SC Malawi) subjected in

183 diverse cowpea accessions and a recombinant inbred line population (RIL) were SNP genotyped using an

184 ulation in rice grain by using a recombinant inbred line population and a backcross introgression lin

185 (Lemont) by indica (Teqing) rice recombinant inbred line population and focused on the genetic variat

186 In a recombinant inbred line population derived from a cross between CDC

187 A recombinant inbred line population derived from a cross between the

188 Using a recombinant inbred line population developed from a lettuce cultivar

189 Screening a recombinant inbred line population developed from PI215246 and cv Sa

190 tures within a Col-0 x Catania-1 recombinant inbred line population identified several loci each of w

191 Japan) x Kas-1 (Kashmir, India) recombinant inbred line population of Arabidopsis thaliana across so

192 Inheritance studies in a recombinant inbred line population of wheat-Ae. peregrina introgress

193 Analysis of a Ler x Sha recombinant inbred line population revealed a single major-effect qu

194 ied by crossing a Columbia x C24 recombinant inbred line population to diploid A. arenosa pollen dono

195 Using a recombinant inbred line population, a separate quantitative trait lo

196 e points from a greenhouse-grown recombinant inbred line population.

197 ines from an independently derived backcross inbred line population.

198 e Arabidopsis thaliana Kas x Tsu recombinant inbred line population.

199 is thaliana) Bayreuth x Shahdara recombinant inbred line population.

200 nt microarray experiments from a recombinant inbred line population.

201 g parents and descendants of two recombinant inbred line populations derived from two weed x crop cro

202 easurement of gene expression in recombinant inbred line populations has enabled investigation of the

203 lyses for seed longevity, in six recombinant inbred line populations, revealed five loci: Germination

204 rlier identified in the same six recombinant inbred line populations.

205 -RIL (nested association mapping-recombinant inbred line) populations indicated that the drl loci res

206 Analysis of recombinant inbred lines provides evidence that the majority of DMRs

207 reating phenotypic differences between these inbred lines provides results concordant with previous a

208 tested with a population of 26 diverse maize inbred lines, R. maidis produced more progeny on those w

209 through chronological sampling of 350 elite inbred lines representing multiple eras of germplasm fro

210 GWAS and analysis of recombinant inbred lines reveal multiple genetic regions underlying

211 ing-(GBS) derived markers to map recombinant inbred line (RIL) and doubled haploid (DH) populations f

212 s) for the interspecific Petunia recombinant inbred line (RIL) population - P. axillaris x P. exserta

213 In this study, we used the recombinant inbred line (RIL) population between Landsberg erecta an

214 used to measure WUE(plant) in a recombinant inbred line (RIL) population created between the C(4) gr

215 ructed a new advanced intercross recombinant inbred line (RIL) population derived from a cross betwee

216 ion responses to priming using a recombinant inbred line (RIL) population derived from a cross betwee

217 ou9308's high yield potential, a recombinant inbred line (RIL) population derived from cross of Xieqi

218 basis of high yield potential, a recombinant inbred line (RIL) population derived from the cross betw

219 cessions, Col-0 and Bur-0, and a recombinant inbred line (RIL) population derived from these parents

220 ng - were employed to genotype a recombinant inbred line (RIL) population developed from a bi-parenta

221 rphisms (SNPs) identified in the recombinant inbred line (RIL) population of ICC 4958 (drought tolera

222 and analyzed in two F(6)-derived recombinant inbred line (RIL) populations derived from the crosses b

223 We used 10 different recombination inbred line (RIL) populations genotyped with high-densit

224 Two sorghum recombinant inbred line (RIL) populations, BTx623/BTx642 and BTx623/

225 2B) to oil quality traits in two recombinant inbred line (RIL) populations.

226 One mapping population of recombinant inbred line (RIL) used in this study was derived from pe

227 Two hundred forty-six recombinant inbred lines (RIL) derived from a cross between Magellan

228 ecture of local adaptation using recombinant inbred lines (RIL) derived from a cross between two loca

229 d four introgressed PM resistant recombinant inbred lines (RIL, USVL531-PMR x USVL677-PMS) were perfo

230 t epigenomic analyses of soybean recombinant inbred lines (RILs) and their parents.

231 ifferent population designs, but recombinant inbred lines (RILs) are among the most effective.

232 polymorphism (SFP) detection in recombinant inbred lines (RILs) can capitalize on the high level of

233 We evaluated recombinant inbred lines (RILs) carrying resistance from S. habrocha

234 netic map of a population of 210 recombinant inbred lines (RILs) derived from a cross between ZS97 an

235 Using a panel of Recombinant Inbred Lines (RILs) derived from a single natural popula

236 ia as well as in a collection of recombinant inbred lines (RILs) derived from indica Jasmine-type var

237 rcross panel consisting of >1600 recombinant inbred lines (RILs) designed for the genetic dissection

238 dence, investigating a subset of recombinant inbred lines (RILs) developed by the Australian peanut b

239 population, consisting of 5,000 recombinant inbred lines (RILs) from 25 families representing the gl

240 ter:sweet compounds by analysing recombinant inbred lines (RILs) from an interspecific lettuce mappin

241 We developed a population of recombinant inbred lines (RILs) originating from a cross between the

242 A careful analysis of two maize recombinant inbred lines (RILs) relative to their inbred parents rev

243 gths and widths in Brassica rapa recombinant inbred lines (RILs) throughout ontogeny.

244 notypically contrasting bulks of recombinant inbred lines (RILs) to identify Pm5e-linked markers.

245 By re-sequencing of 138 recombinant inbred lines (RILs), a total of ~0.7 million SNPs were i

246 munity consisting of two sets of recombinant inbred lines (RILs), each derived from an advanced gener

247 , as well as in two derivative recombination inbred lines (RILs).

248 ments from seedlings in a variety of Pioneer inbred lines, routinely recovering healthy, fertile T0 p

249 rawberries (Fragaria vesca f. semperflorens) inbred lines-Ruegen F7-4 (a red-fruited genotype) and YW

250 anisms of differential infection of Zea mays inbred line SDp2 by Wheat streak mosaic virus (WSMV) iso

251 tential hybrids derived from 210 recombinant inbred lines, selection of the top 10 hybrids predicted

252 These inbred lines share common ancestry, and only 13% of thei

253 duction fixes recombinant haploid genomes in inbred lines, shaving years off the breeding process.

254 Inbred lines showed higher signed FA variances (16 and 3

255 lly expressed genes between the two parental inbred lines significantly exceeded those of parent vers

256 d the number of active genes in the parental inbred lines significantly independent of treatment.

257 lone establishes systemic infection in maize inbred lines, sorghum (Sorghum bicolor), and green foxta

258 Highly recombinant populations derived from inbred lines, such as advanced intercross lines and hete

259 e segment substitution lines and backcrossed inbred lines suggested that NOMT is the underlying cause

260 number of recombinant events in recombinant inbred lines suggests that for a biparental population w

261 00 years has produced elite maize (Zea mays) inbred lines that combine to produce high-yielding hybri

262 ryos under investigation were from a pair of inbred lines that had been artificially selected for egg

263 In 368 maize inbred lines, the circRNA-hosting genes were enriched fo

264 ed mass features were present in >90% of the inbred lines, the majority were found in <50% of the sam

265 ng of seedling RNA from 503 maize (Zea mays) inbred lines to characterize the maize pan-genome, we id

266 creened a panel of sorghum (Sorghum bicolor) inbred lines to identify and characterize sorghum tolera

267 We used maize (Zea mays) recombinant inbred lines to map a quantitative trait locus (QTL) for

268 We used genetically distinct maize inbred lines to perform two crossing experiments.

269 tically variable transcripts in wild-derived inbred lines to predict coregulated transcriptional netw

270 c distance estimators between pairs of maize inbred lines to predict genotypic variation for quantita

271 he dek phenotypes were introgressed into two inbred lines to take advantage of maize haplotype variat

272 sed transgressive segregation in recombinant inbred lines to test if this apparent species-wide (nonh

273 opulations created by crossing two temperate inbred lines to two photoperiod-sensitive tropical inbre

274 on tests on the maize-282-diverse-panel (282 inbred lines) under normal (25 degrees C) and chilling (

275 e inferred in silico based on their parental inbred lines using single nucleotide polymorphisms (SNPs

276 y 313.4-Mb genome sequence of a bottle gourd inbred line, USVL1VR-Ls, with a scaffold N50 of 8.7 Mb a

277 Progeny from crosses between various inbred lines vary in the extent of vigor observed.

278 Here, a set of 289 diverse maize inbred lines was genotyped with 56,110 SNPs and assayed

279 because genetic variation among wild-derived inbred lines was much lower than predicted from a neutra

280 -induced volatiles among 26 maize (Zea mays) inbred lines, we conducted a nested association mapping

281 conditions in three Brachypodium distachyon inbred lines, we describe the identification and the mai

282 rom our analysis of a diverse panel of maize inbred lines, we discovered high positive genetic correl

283 Exploiting wild accessions and recombinant inbred lines, we reveal extensive phenotypic variation i

284 from ear, tassel, and leaf of the B73 public inbred line were constructed at four developmental stage

285 expected heterozygosity (He) in these highly inbred lines were 0.291 and 0.359, respectively, which i

286 INERA and 41 exotic (temperate and tropical) inbred lines were characterized using 1057 SNP markers t

287 ve tissues from 27 genetically diverse maize inbred lines were deeply sequenced to identify genes exh

288 genome resequencing data from 61 additional inbred lines were enriched in organ-specific and stress-

289 closely examined beta-costic acid-deficient inbred lines were found to harbor Zmtps21 pseudogenes la

290 ed differentially to stress between parental inbred lines were identified.

291 s of DNA methylation for 20 maize (Zea mays) inbred lines were used to discover differentially methyl

292 f 15.78 megabases) of the maize small-kernel inbred line, which is derived from a tropical landrace.

293 l root length' (TRL) were predicted for 2431 inbred lines, which had previously been genotyped by seq

294 using mixed sequence data of two Drosophila inbred lines, which was a novel validation approach for

295 There was genetic diversity among INERA inbred lines, which were genetically less closely relate

296 ny times in parallel, to create a new set of inbred lines whose genomes are random mosaics of the gen

297 F(1) individuals derived from these inbred lines will be hemizygous for each of these non-al

298 ng of 200 Drosophila Genetic Reference Panel inbred lines with complete genome sequences and for whic

299 encapsulation ability of crickets from eight inbred lines with that of crickets from the outbred foun

300 istory in a set of Brassica rapa recombinant inbred lines within and across field and greenhouse envi