ライフサイエンスコーパス: inbred

1 ales and females: CD1 (outbred) and C57BL/6 (inbred).

2 pression of the drl2-Mo17 allele in the Mo17 inbred.

3 Although the index animal was partly inbred, 58% of the genome was haplotype-phased by FALCON

4 report that non-GT cells of self-pollinated inbred A. annua plants can express the artemisinin biosy

5 n are localized in non-GT cells of leaves of inbred A. annua plants.

6 pathway genes in GT-free leaves and calli of inbred A. annua plants.

7 cted parental haplotypes, which revealed the inbred ancestry of infections and non-Mendelian inherita

8 are expressed in at least one tissue of one inbred and an additional ~10 000 "silent" genes that are

9 Both the C57BL/6 inbred and BALB/cBy congenic UBC-GFP lines are commercia

10 ders of the known pedigree may themselves be inbred and compute the appropriate inbreeding-adjusted k

11 of germination under anaerobic conditions in inbred and hybrid rice varieties.

12 ity, and its domestication has produced many inbred and outbred lines that are used for different pur

13 and severity of silicosis was determined in inbred and outbred mice.

14 We discovered that both inbred and outbred rats could shorten the duration of SW

15 uma.SIGNIFICANCE STATEMENT Our evidence that inbred and outbred rats learn to control the duration of

16 Finally, NAT pairs in 368 diverse maize inbreds and 19 segregating populations were specifically

17 n hybrids through the crossing of 593 unique inbreds and 496 unique testers across multiple environme

18 anscriptome data of diverse Zea mays (maize) inbreds and hybrids, including 401 samples from five dif

19 , and 24-nt sRNAs varies very little between inbreds and hybrids, suggesting that hybridization affec

20 ed with their frequency of dispersion across inbreds and on average have significantly fewer co-expre

21 e of a list of potential breeding crosses of inbreds and testers based on their historical yield data

22 Here, two genomes for Mo17 (a modern maize inbred) and mexicana are assembled using a meta-assembly

23 and between plant genetic groups (teosinte, inbred, and modern hybrid).

24 Inbred animals were historically chosen for genome analy

25 opulation sequence data from 488 recombinant inbred Arabidopsis thaliana genomes, we identified 6502

26 matography analyses demonstrate that the two inbreds are highly differentiated in their metabolite pr

27 d trait is robust as it improves yield in an inbred as well as in a panel of hybrids, at several loca

28 hibited substantially more variation between inbreds as compared with observed variation for gene exp

29 omosomally anchored the nuclear genome of an inbred B. pendula individual.

30 n annotated in the reference genome of maize inbred B73.

31 ntal gradient from four maize genotypes (the inbreds B73 and Mo17, and the reciprocal hybrids B73 x M

32 (oligos) specific to chromosome 10 of maize inbreds B73 and Mo17, respectively, are synthesized and

33 ion of gene expression between the two maize inbreds B73 and Mo17.

34 tissues or developmental stages of two maize inbreds, B73 and Mo17, as well as their F(1) hybrid.

35 Mutator (Mu) insertional library in the B73 inbred background designated BonnMu A total of 1,152 Mu-

36 ity, and phenotypic severity is dependent on inbred background.

37 d analyzed the Lgn-R phenotype in additional inbred backgrounds.

38 ection into male and female immune-competent inbred BALB/c mice.

39 Rats of the inbred BD strains postnatally exposed to the carcinogen

40 uency spectrum at equilibrium, given a fully inbred breeding design.

41 eding strategy between outbred CD-1 mice and inbred C57-based Cre lines that can be used to study cel

42 Interestingly, ~25% of inbred C57BL/6 mice fail to respond to aggression traini

43 d qMotor in SOD1(G93A) transgenic mice in an inbred C57BL/6J background, hereafter called iSOD1(G93A)

44 s (CC) mouse strains, as well as the classic inbred C57BL/6J, C3H/HeJ, and BALB/cJ strains, for scree

45 ring loss disrupts high-frequency hearing in inbred CD-1 mice.

46 We challenged birds sampled from a highly inbred chicken line (line 6(3)) that is relatively resis

47 g ASE in F1 reciprocal crosses of two highly inbred chicken lines (Fayoumi and Leghorn).

48 tion using next generation sequencing on the inbred chicken lines with the assistance of CNVnator.

49 Two highly inbred chicken lines, 6(3) (MD-resistant) and 7(2) (MD-s

50 The A619 inbred contains a nonfunctional Ven1 allele, leading to

51 Our results suggest that inbred cooperative societies are rare in nature partly b

52 The inbreds could be vital sources of beneficial alleles for

53 transgenic hybrid breeding strategy crossing inbred Drd1-Cre and Drd2-Cre transgenic mice with outbre

54 n changed in a population of fully sequenced inbred Drosophila melanogaster strains when flies develo

55 ple stages of metazoan development, using 80 inbred Drosophila wild isolates, identifying thousands o

56 and populations include inbred, recombinant inbred, F1 hybrid, transgenic, targeted mutants, chromos

57 QTL) analysis of an intra-Andean recombinant inbred family derived from a landrace and a wild accessi

58 tribute to differential resistance to NDV in inbred Fayoumi and Leghorn lines.

59 The inbred Fischer 344 rat is being evaluated for testing no

60 with single-cell mRNA sequencing of the same inbred fly strain to map transposon expression in the Dr

61 We evaluated evidence in the B73 Zea mays inbred for differences in the activity of the UPR betwee

62 7a7Bay/Bay mice on the C57BL/6 and C57BL/6NJ inbred genetic backgrounds, respectively.

63 inbred mouse strains and mutations placed on inbred genetic backgrounds.

64 An assembly of the single-haplotype inbred genome of cowpea IT97K-499-35 was developed by ex

65 architectures (RSAs) of two maize (Zea mays) inbred genotypes and their hybrid as they grew in comple

66 n profiling for a diverse panel of 263 maize inbred genotypes.

67 cies, and then further grouped into distinct inbred genotypes.

68 been constructed in crop species, and their inbred germplasm and associated phenotypic and genotypic

69 Four of the inbreds had significant positive general combining abili

70 itutions between restoring and non-restoring inbreds, however only one substitution, F187Y, was withi

71 ygosity found in the genomes of particularly inbred individuals and of domestic animals can skew esti

72 Inbreeding depression occurs when inbred individuals experience reduced fitness as a resul

73 s of realized inbreeding, we discovered that inbred individuals had lower survival probabilities and

74 However, as adults, inbred individuals provide less care, reducing the amoun

75 ygosity of putatively deleterious alleles in inbred individuals.

76 tation process and on the possible basis for inbred instability in maize.

77 studies have been largely carried out using inbred isogenic mouse strains, in which there is no (or

78 tes to immune system maturation by releasing inbred laboratory mice into an outdoor enclosure.

79 t individual female Drosophila from a highly inbred laboratory strain exhibit idiosyncratic odor pref

80 Rats (inbred: LEW, WKY, F344/ICO and F344/DU, outbred: Crl:SD)

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

101 ines from an independently derived backcross inbred line population.

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

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

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

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

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

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

108 ntrogressed into a disease-susceptible maize inbred line.

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

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

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

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

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

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

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

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

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

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

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

120 146 maize genotypes comprising of landraces, inbred lines and commercial hybrids.

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

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

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

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

125 Other inbred lines are known to transcribe significantly diffe

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

174 limited variations in their boundaries among inbred lines.

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

176 scriptome-wide association studies using 505 inbred lines.

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

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

179 support a global selective sweep of a highly inbred livestock pathogen that originated within Europea

180 le of balancing selection in maintaining the inbred load and linked genetic diversity.

181 he butterfly Bicyclus anynana carries a high inbred load for male fertility and viability.

182 nes, dRemp is highly mobile in the Corn Belt inbred M14, identified earlier by breeders as being high

183 on, comparative optical mapping of two other inbred maize lines revealed a prevalence of deletions in

184 more than 2.5-fold across a diverse group of inbred maize lines were resolved.

185 that microbial co-occurrence patterns of the inbred maize lines' rhizosphere were significantly more

186 PR-Cas9 editing of a waxy allele in 12 elite inbred maize lines, a process that was more than a year

187 n evolutionary transect (two teosinte, three inbred maize lines, and five modern maize hybrids) grown

188 We employed a SEFL paradigm in inbred male and female C57BL/6 mice that combines acute

189 use computational analysis of 13 recombinant inbred mapping populations to assess crossover and gene

190 inbreeding coefficient were used to prohibit inbred marriages and prohibit breeding of some pairs of

191 show that B cells and serum antibodies from inbred mice demonstrate a reproducible ID hierarchy to t

192 For over a century, inbred mice have been used in many areas of genetics res

193 er liver or brain tissues of BXD recombinant inbred mice in the GeneNetwork database.

194 alizability of any genetic research study in inbred mice is dependent upon all individual mice being

195 Inbred mice that lack the gene encoding nitric oxide syn

196 ss-enhanced fear learning (SEFL) paradigm in inbred mice that produces PTSD-like characteristics in a

197 he breeding designs of companies that supply inbred mice to researchers.

198 Treatment of obese inbred mice with RvE1, the downstream immunoresolvant me

199 ed the development of animal models, such as inbred mice, to define mechanisms of immunity.

200 design IMPLICON for ICRs in adult tissues of inbred mice, validating it in hybrid mice from reciproca

201 occurring genetic variation in wild-derived inbred mice, which enables the identification of DNA seq

202 riety of tissues across genetically distinct inbred mice.

203 in an inbred strain but fully lethal in non-inbred mice.

204 tes that cause different disease symptoms in inbred mice.

205 kinetics, plaque size, and pathogenicity in inbred mice.

206 lled system of administered immunizations to inbred mice.

207 rized mouse AD models into three groups: (i) inbred models, (ii) genetically engineered mice in which

208 Genetic differences between inbred mouse models and the outbred human population and

209 dress this issue; discuss the limitations of inbred mouse models of monocyte-macrophage homeostasis;

210 mRNA) sequencing datasets from a recombinant inbred mouse panel.

211 Here, we exploited robust inbred mouse strain differences in Pavlovian fear extinc

212 mouse strain, and the mtDNA from a different inbred mouse strain to examine the genome-wide nuclear D

213 mice, that contain the nuclear DNA from one inbred mouse strain, and the mtDNA from a different inbr

214 +) T cells compared to a resistant classical inbred mouse strain.

215 translational studies utilize only a single inbred mouse strain.

216 dogenes in the mouse reference genome and 18 inbred mouse strains (available via the mouse.pseudogene

217 ZIKV exposure in four genetically divergent inbred mouse strains (C57BL/6J, 129S1/SvImJ, FVB/NJ, and

218 audi chabaudi AS in early gestation, several inbred mouse strains abort at midgestation.

219 We surveyed 120 inbred mouse strains and found that the frequency of adu

220 hese assays are ubiquitously performed using inbred mouse strains and mutations placed on inbred gene

221 ng inflammation and toxicity across multiple inbred mouse strains and to use genome-wide association

222 st several days of infection.IMPORTANCE Most inbred mouse strains are relatively resistant to orthopo

223 The very closely related inbred mouse strains BALB/cJ and BALB/cByJ differ substa

224 , a powerful genetic resource of recombinant inbred mouse strains derived from eight diverse founder

225 We used a family of recombinant inbred mouse strains for interval mapping and to examine

226 rformed quantitative trait locus analysis in inbred mouse strains that carry the same hypomorphic all

227 aborative Cross (CC), a panel of recombinant inbred mouse strains that exhibit a range of disease man

228 transcription factors between crosses of two inbred mouse strains to elucidate the regulatory mechani

229 ing cis-regulatory variation in wild-derived inbred mouse strains to explore the mechanisms underlyin

230 tinal ganglion cell (RGC) function in common inbred mouse strains using the pattern electroretinogram

231 RORgamma(+) Treg proportions varied between inbred mouse strains, a trait transmitted by the mother

232 nitor differentiation from the marrow of two inbred mouse strains, C3H/HeJ (C3H) and C57BL6J (B6).

233 e genomic DNA methylation by intercrossing 2 inbred mouse strains, C57BL/6N and C3H/HeN, and analyzin

234 ough urinary Mup protein levels vary between inbred mouse strains, this difference is most pronounced

235 ze in vitro differentiated Th1 cells from 16 inbred mouse strains.

236 this finding was replicated in a study of 98 inbred mouse strains.

237 iet (HCD), we quantified food-intake in four inbred mouse strains: C57Bl/6J (B6), NOD/LtJ (NOD), 129S

238 ions of germinating seeds from two different inbreds of maize (Zea mays) seeds, B73 and Mo17.

239 maize hybrids generated by crossing founder inbreds of nested association mapping populations for fl

240 growth using maize overexpression (OE; B104 inbred) or knockout (KO; W22 inbred) lines.

241 individuals from three genetic backgrounds (inbred - outbred) into a novel environment at three foun

242 p between Wolbachia and mtDNA, using a large inbred panel of Drosophila simulans.

243 en 18 diverse inbred lines and the recurrent inbred parent B73, referred to as the nested NILs (nNILs

244 of residual heterozygosity identified in the inbred parental parent (M6).

245 ys) samples spanning five tissues from eight inbred parents and 12 hybrid genotypes, covering a spect

246 rved between the genetic distance of the two inbred parents and the number of SPE genes identified.

247 core genes conserved across the 62 profiled inbreds, PAVs have lower expression abundances which are

248 dulating (nod-) and nodulating (nod+) sister inbred peanut lines, E4/E5 and E7/E6, and their nod+ par

249 ecular findings of Hereditary Myotonia in an inbred pedigree.

250 ceptible) were used to develop a recombinant inbred population with future goals of identifying genom

251 Finally, inbred populations with a high prevalence of obesity pro

252 Here, we used inbred rat models of kidney damage associated with eleva

253 We hypothesized that inbred rat strains possessing stress hyper-reactive-, de

254 ear equivalent to those found in outbred and inbred rat strains, except for lower incidence and short

255 lepsy and are used to model this disorder in inbred rats.

256 Strain types and populations include inbred, recombinant inbred, F1 hybrid, transgenic, targe

257 Here, we determined whether BXD recombinant inbred (RI) mice strains are more suitable than C57BL/6J

258 The highly resistant recombinant inbred RIL 46 and moderately resistant RIL 48 were selec

259 ting IBD-based methods are limited to highly inbred samples, or lack robustness to genotype error and

260 nging to understand the persistence of these inbred societies in nature.

261 that offsets inbreeding depression, allowing inbred societies to evolve.

262 nes in additional inbred lines, arising from inbred-specific DNA methylation patterns.

263 Furthermore, use of an inbred strain allows for investigation into epigenetic m

264 mouse was initially generated in the C57BL/6 inbred strain and has been backcrossed into the BALB/cBy

265 However, ground state pluripotency in some inbred strain backgrounds is unstable in the absence of

266 defects, which are partially penetrant in an inbred strain but fully lethal in non-inbred mice.

267 identical to that of any other CC strain or inbred strain for which prior data are available, indica

268 sting using multiple genotypes revealed that inbred strain siblings do not cooccupy at higher rates t

269 The castaneous (CAST) mouse, a wild-derived inbred strain, is highly susceptible to orthopoxvirus in

270 mice from an advanced intercross between two inbred strains (LG/J and SM/J); this GWAS identified 23

271 cly available genome sequences of 36 popular inbred strains and provide lists for each strain of prot

272 heritable trait by using female rats of six inbred strains and six F1 hybrids.

273 Genetically diverse inbred strains are frequently used in quantitative trait

274 enetic studies involving a cross between two inbred strains are usually followed by congenic mapping

275 he hybrid mouse diversity panel (HMDP) of 83 inbred strains as a surrogate for human natural immune v

276 ted the hypothesis that genetic variation in inbred strains of mice influences the innate variability

277 r this study, we collected microbiota from 2 inbred strains of mice which differ in adiposity and glu

278 ity and mosaic regularity across recombinant inbred strains of mice, finding that, although both trai

279 Diversity Panel data, which consisted of 100 inbred strains of mice, we identified 97 DMCs that were

280 under genetic regulation and differs between inbred strains of mice.

281 Female mice of 28 inbred strains received this vaccine at 6, 8, and 12 wee

282 Mouse inbred strains remain essential in science.

283 However, comparison of five common inbred strains revealed a disparity in precursor-product

284 ences from individuals of four commonly used inbred strains that were procured from either the colony

285 fter assigning female mice from 29 different inbred strains to normal chow or lithium diet (40 mmol/k

286 449 male mice from 33 inbred strains underwent MCAO for 6 hours (215 mice) or

287 th the use of a panel of MHC-III recombinant inbred strains, we found that the 33-kb Ltab-Ncr3 haplot

288 sequenced classical and high-priority mouse inbred strains.

289 s of innate immune genes to NDV infection in inbred sublines of the Fayoumi and Leghorn breeds known

290 ry rats and possibly to those that have been inbred to model absence epilepsy.SIGNIFICANCE STATEMENT

291 As inbred trisomic mice also exhibit variable phenotypes, w

292 x favorable homeoallelic interactions within inbred varieties.

293 boratory outbred BN, outbred Long-Evans, and inbred WAG/Rij rats (i.e., a model of absence epilepsy).

294 s, Sprague Dawley and Long-Evans, and/or the inbred WAG/Rij strain (a rat model of heritable human ab

295 bred BN rats than the outbred Long-Evans and inbred WAG/Rij strains.

296 10 296 310 SNPs available from the parental inbreds, we explored the patterns of genomic relationshi

297 Genetic analysis of a recombinant inbred wheat population inoculated separately with three

298 ilar to the distribution in the B73 parental inbred, whereas that of Mo17 x B73 resembles the Mo17 pa

299 in 4Co63, but not at all in B73 or Mo17, two inbreds widely represented in Corn Belt hybrids.

300 se transcript pairs (NAT pairs) in two maize inbreds with different sensitivity to drought, as well a