ライフサイエンスコーパス: inbred line

1 sava and comparative analyses with a partial inbred line.

2 sing genetically modified substrains of this inbred line.

3 root tip metaphase chromosomes from the B73 inbred line.

4 other flavonols were identified in these two inbred lines.

5 of sequence variants among these widely used inbred lines.

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

7 ion differences are inherited by recombinant inbred lines.

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

9 panel of Drosophila melanogaster recombinant inbred lines.

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

11 nt inbred line families derived from diverse inbred lines.

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

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

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

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

16 ation in populations generated from multiple inbred lines.

17 evant traits in D. melanogaster wild-derived inbred lines.

18 e tested show +/- polymorphisms among modern inbred lines.

19 1500 outcrossed mice originating from eight inbred lines.

20 ollinearity reported between different maize inbred lines.

21 assays and DNA sequencing in different maize inbred lines.

22 W23 were examined for NUMT variation within inbred lines.

23 also has elevated maternal care relative to inbred lines.

24 of which were polymorphic among a sample of inbred lines.

25 generating populations of highly recombinant inbred lines.

26 on the qualities of the final population of inbred lines.

27 le nucleotide polymorphisms) between the two inbred lines.

28 f wild teosintes, maize landraces, and maize inbred lines.

29 aluated on a population of wheat recombinant inbred lines.

30 neration of genetic variability, even within inbred lines.

31 markers on 95 single-chromosome recombinant inbred lines.

32 e applicable only to genetic crosses between inbred lines.

33 outbred broiler sires to dams of two highly inbred lines.

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

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

36 numerous previously non-transformable maize inbred lines.

37 gene variants present in the many available inbred lines.

38 ompared with B73 and Tx601 maize susceptible inbred lines.

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

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

41 leotide diversity was only slightly lower in inbred lines ( = 0.0094) than wild populations ( = 0.012

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

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

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

45 Inbred lines A188 and B73 were cultivated under sufficie

46 applied to chromosome spreads of ten diverse inbred lines: A188, A632, B37, B73, BMS, KYS, Mo17, Oh43

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

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

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

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

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

52 behavior in a population of 41 wild-derived inbred lines and asked to what extent different larval-r

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

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

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

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

57 two sets of Arabidopsis thaliana recombinant inbred lines and have identified 14 QVE (quantitative vi

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

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

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

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

62 ionally silent and methylated states in some inbred lines and unmethylated, expressed states in other

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

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

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

66 mal clusters in a population of wild-derived inbred lines, and asked whether polymorphisms in these g

67 For those organisms where recombinant inbred lines are available for mapping, the "distant pai

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

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

70 ce analyses of the "gene space" of the maize inbred line B73 genome, coupled with wet lab validation,

71 utagenized population derived from the maize inbred line B73.

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

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

74 ys were hybridized with RNA samples from the inbred lines B73 and Mo17 and from near-isogenic derivat

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

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

77 d from endosperm tissues of maize (Zea mays) inbred lines B73 and Mo17 and their reciprocal hybrids a

78 Hybrids between the maize inbred lines B73 and Mo17 exhibit heterosis regardless o

79 The maize inbred lines B73 and Mo17 produce a heterotic F1 hybrid.

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

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

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

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

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

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

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

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

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

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

90 restoring allele traceable to either of two inbred lines, C103 and Oh40B.

91 rified BGAF to homogeneity from a maize null inbred line called H95.

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

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

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

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

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

97 for quantitative trait loci (QTL) mapping in inbred line crosses.

98 te high and low LD populations from multiple inbred line crosses: the first included many small full-

99 Ler, but not of FRL2-Col, into a recombinant inbred line derived from these plants restores both FRI-

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

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

102 Recombinant inbred lines derived from an advanced intercross, in whi

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

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

105 Twenty inbred lines derived from nature were measured for their

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

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

108 istribution with power-law scaled tails, the inbred lines derived from the wild stock were dramatical

109 Most frequently, recombinant inbred lines derived from two isogenic parents are used.

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

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

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

113 QTL mapping with recombinant inbred lines detected 12 major QTL for 11 of the 13 edit

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

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

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

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

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

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

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

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

122 1-2 (ddm1-2)-derived epigenetic recombinant inbred lines (epiRILs) in Arabidopsis thaliana is well s

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

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

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

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

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

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

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

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

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

132 We derived inbred lines from ancestral and evolved populations and

133 ral accession and populations of recombinant inbred lines from over 800 separate experiments, represe

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

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

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

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

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

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

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

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

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

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

144 lianthus annuus L.) cultivars (elite oilseed inbred lines) has been shaped by domestication and breed

145 phenomenon whereby the progeny of particular inbred lines have enhanced agronomic performance relativ

146 models to analyze data from eight segmental inbred lines in a B73 background and their crosses to th

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

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

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

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

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

152 been developed using intermated recombinant inbred lines (IRILs) from the intermated B73xMo17 (IBM)

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

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

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

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

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

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

159 41 genes in one or more of three recombinant inbred line mapping populations, thus providing a pictur

160 n of the bz genomic regions of two different inbred lines, McC and B73.

161 ethod to a maize RIL population derived from inbred lines Mo17 and B73 and developed by selfing sugge

162 sis using map-based cloning with recombinant inbred lines, natural variation transcriptomic analysis,

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

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

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

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

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

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

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

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

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

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

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

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

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

176 eactivity) in a population of 98 recombinant inbred lines of Drosophila melanogaster and mapped four

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

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

179 om both wild populations and four moderately inbred lines of Drosophila simulans.

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

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

182 of shoot apical meristems isolated from two inbred lines of maize using laser capture microdissectio

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

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

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

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

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

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

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

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

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

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

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

194 None of the tested inbred lines other than B73 showed the strong hybridizat

195 To develop inbred lines, parents are crossed to generate segregatin

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

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

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

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

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

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

202 pulation, an advanced intercross recombinant inbred line population derived from a cross between the

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

204 time gene SNPs in an independent recombinant inbred line population derived from the intercrossing of

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

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

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

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

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

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

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

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

213 nt microarray experiments from a recombinant inbred line population.

214 ss population and a conventional recombinant inbred line population.

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

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

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

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

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

220 Intercrosses between inbred lines provide a traditional approach to analysis

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

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

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

224 0 and 280,000 454 ESTs from the B73 and Mo17 inbred lines, respectively.

225 previous Ler x Col and Cvi x Ler recombinant inbred line (RIL) mapping studies, no additive QTL overl

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

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

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

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

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

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

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

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

234 merated between two parents of a recombinant inbred line (RIL) population segregating for several imp

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

236 2B) to oil quality traits in two recombinant inbred line (RIL) populations.

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

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

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

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

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

242 ir allometric relationship using recombinant inbred lines (RILs) derived from a natural population in

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

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

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

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

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

248 TL) influencing recombination in recombinant inbred lines (RILs) is proposed that relies upon the fac

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

265 s developed based on experimental crosses of inbred line species in backcross populations.

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

267 LD decayed more slowly in inbred lines than wild populations (mean LD declined to

268 00 years has produced elite maize (Zea mays) inbred lines that combine to produce high-yielding hybri

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

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

271 the maize chromomethylase ZMET2 in multiple inbred lines to determine whether epigenetic changes con

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 Marker data on 42 two-row spring barley inbred lines were used to simulate high and low LD popul

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 ctive capabilities of the model with a maize inbred line, Wisconsin 22, and found it to be accurate i

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