ライフサイエンスコーパス: linkage mapping

1 f resulting progeny were analyzed by genetic linkage mapping.

2 deep shotgun sequencing and high-resolution linkage mapping.

3 agments that was not resolved by the genetic linkage mapping.

4 16 origin of clones was confirmed by genetic linkage mapping.

5 the critical region through YAC content and linkage mapping.

6 cannabinoid synthase genes and were used in linkage mapping.

7 and dry weight accumulation under low P via linkage mapping.

8 nd conducted both single- and combined-cross linkage mapping.

9 re rapid and cost-effective than traditional linkage mapping.

10 assisted bulk segregant analysis followed by linkage mapping.

11 lucidate regulatory networks and can improve linkage mapping.

12 eviously on the basis of comparative genetic linkage mapping.

13 d from varieties AU9 and SunUp were used for linkage mapping.

14 orin-2 (Aqp2) in cph mutants through genetic linkage mapping.

15 an average of 8.2 AFLP markers eligible for linkage mapping.

16 e use of positional cloning, which relies on linkage mapping.

17 tified, which were subsequently validated by linkage mapping.

18 biased estimation and reduced efficiency in linkage mapping.

19 characterized the rc phenotype and initiated linkage mapping.

20 nd suggests a new mathematical framework for linkage mapping.

21 e sibling-pair cohort was subjected to finer linkage mapping.

22 Guided by findings in linkage mapping, a genome-wide association study of plan

23 of population size and number of markers on linkage mapping accuracy.

24 The robustness of parametric linkage mapping against model misspecification is consid

25 Linkage mapping analyses indicated very little genetic i

26 Using genome-wide linkage mapping and a positional candidate approach in a

27 Using genome-wide linkage mapping and a positional candidate approach, we

28 e a source of powerful molecular markers for linkage mapping and biodiversity studies.

29 Through linkage mapping and complementation testing, we identifi

30 ing, but also complementarity to traditional linkage mapping and cytogenetic methods.

31 Linkage mapping and genome-wide association studies of A

32 ith, recombination mapping, in terms of both linkage mapping and linkage disequilibrium mapping.

33 associated DNA (RAD) genotyping, traditional linkage mapping and multivariate image analysis to study

34 nd tetrasomic has important implications for linkage mapping and population genetics and hence breedi

35 pective on the challenges of moving from the linkage mapping and positional cloning studies on which

36 r high-throughput genotyping as required for linkage mapping and profiling genetic variation in natur

37 Here, we used linkage mapping and quantitative trait locus (QTL) mappi

38 rican families with the RP10 form of adRP by linkage mapping and used these families to reduce the li

39 Linkage mapping and whole-exome sequencing identified ho

40 Through genetic linkage mapping and whole-exome sequencing, we identifie

41 rom 55 family members (UM:H389) was used for linkage, mapping, and mutation analysis.

42 able for genome-wide high-resolution genetic linkage mapping, by recurrent intermating among F2 indiv

43 n experiments, STS-based PCR assays, genetic linkage mapping, cDNA localization, and FISH data.

44 Using a unique property of multiparental linkage mapping designs, for each QTL we highlight a rel

45 Chromosome assignment of markers based on linkage mapping differed from sequence alignment with th

46 nd ataxia, where either clinical features or linkage mapping excluded known PME loci.

47 Through association analysis, linkage mapping, expression analysis, and mutagenesis, w

48 bridization, and all the markers assigned by linkage mapping fall within a 1.6-cM interval.

49 Linkage mapping finds a significant interaction effect f

50 We used a combination of linkage mapping, genome-wide association studies (GWAS),

51 Traditionally, linkage mapping has been the most commonly employed meth

52 Dense linkage mapping has highlighted the presence of 2 loci o

53 Genetic linkage mapping has identified more than 100 plant resis

54 Linkage mapping has previously shown convergent red wing

55 Genotyping, as applied to linkage mapping, human identification, or mapping of gen

56 ide association and targeted high-resolution linkage mapping identified ZmCCT, a homologue of the ric

57 Genome-wide linkage mapping identifies a single chromosome region at

58 Genome-wide linkage mapping identifies largely separate sets of quan

59 These results demonstrate the utility of linkage mapping in a human helminth parasite, while crys

60 P (adRP) was placed on chromosome 17p13.3 by linkage mapping in a large South African adRP family.

61 Using genome-wide linkage mapping in marine-freshwater F2 genetic crosses,

62 ncertainty about linkage phases of founders, linkage mapping in nonmodel, outcrossing systems using m

63 Statistical analyses for linkage mapping in polyploid species can be difficult du

64 t covers existing statistical approaches for linkage mapping in polyploids that are predominantly mul

65 Here, we report the use of linkage mapping in synthetic F2 populations and compleme

66 Family-nested QTL were identified by joint-linkage mapping in the NAM panel.

67 Linkage mapping in two species groups, gene-expression a

68 Linkage mapping indicates that the modifying gene is ver

69 show that association mapping combined with linkage mapping is a powerful method to discover importa

70 High-density genetic linkage mapping is a valuable and effective method for e

71 der of genes in genomes for which gene-based linkage mapping is impractical.

72 studies of rare diseases, the resolution of linkage mapping is limited by the number of available me

73 Moreover, linkage mapping is one of the best ways to detect errors

74 The goal of linkage mapping is to find the true order of loci from a

75 s of the crossover events and the multipoint linkage mapping localized the disease locus to an 8.8-cM

76 ing nullisomic deletion mapping with meiotic linkage mapping, loci known to be located on a particula

77 Linkage mapping methods have identified major-effect eQT

78 ial value of recently developed high-density linkage mapping methods in the analysis of complex disea

79 This study describes the physical and linkage mapping of 42 gene-associated markers developed

80 Exclusion linkage mapping of chromosome 16 was performed in a sepa

81 Linkage mapping of complex diseases is often followed by

82 AP-O-MAT is a web-based server for automated linkage mapping of human polymorphic DNA markers.

83 We then performed genetic linkage mapping of male-specific traits important for re

84 Linkage mapping of methylation states assessed from whol

85 ased association mapping and of family based linkage mapping of quantitative traits in humans.

86 ws the challenges we face in moving from the linkage mapping of susceptibility genes for type 2 diabe

87 Reported herein is linkage mapping of the H locus to a 3.27 Mb region of ch

88 otide polymorphism (SNP) assays designed for linkage mapping of the human genome.

89 We further report linkage mapping of the primary cea locus to a 3.9-cM reg

90 Genetic linkage mapping of two crosses showed dominance of male

91 ustrate an approach to combined physical and linkage mapping of type 1 anchor (gene) loci in the dog

92 ntified by whole-genome sequencing following linkage mapping or by whole-exome sequencing.

93 linkage mapping set, the Illumina BeadArray linkage mapping panel (version 3) and the Affymetrix Gen

94 is, we have genotyped the Illumina BeadArray linkage mapping panel (version 4) in a data set of 730 m

95 Linkage mapping placed Pafaha-ps1 and Pafaha-ps2 to dist

96 By integrating linkage mapping, polyploid phylogeny and sex-determining

97 ii and M. cardinalis was explored in a large linkage mapping population of F2 plants n = 465 to provi

98 The implications of this model for linkage mapping, population genetic studies, and polyplo

99 Historically, linkage mapping populations have consisted of large, ran

100 re incorporated in our new, freely available linkage-mapping program MULTIGENE 1.0 for the PC environ

101 y found specific polymorphic markers for our linkage mapping project.

102 t, a combination of correlation analysis and linkage mapping provides the potential to identify and s

103 We selected 7,734 SNPs for linkage mapping, resulting in 27 linkage groups with a m

104 The comparative linkage mapping results indicate that the q arm of human

105 Joint-linkage mapping revealed that the genetic architecture o

106 Linkage mapping revealed that two point mutations are re

107 nt microsatellite markers from the ABI Prism linkage mapping set v.2 on an ABI 377 sequencer/genotype

108 For the microsatellites, the ABI Prism Linkage Mapping Set version 2, with 402 microsatellite m

109 ted relatives per family using the ABI Prism linkage mapping set which includes 350 polymorphic marke

110 plied Biosystems high-density microsatellite linkage mapping set, the Illumina BeadArray linkage mapp

111 n an Applied Biosystems model 377 (ABI PRISM Linkage Mapping Sets; Perkin Elmer Applied Biosystems),

112 Linkage mapping showed that body weight (BW) loci on pro

113 Genome-wide linkage mapping shows that pelvic reduction is controlle

114 Here we present a linkage mapping software Lep-MAP3, capable of mapping hi

115 Linkage mapping studies in model organisms have typicall

116 duced and form a unique resource for genetic linkage mapping studies in the horse.

117 e results demonstrate the benefits for horse linkage mapping studies of genotyping on these unique fu

118 ted genetic maps can have adverse effects on linkage mapping studies.

119 bined fluorescence in situ hybridization and linkage mapping, the gene order on CFA9 is similar to th

120 By linkage mapping, the transgene integration site was loca

121 the utility of these data in high-resolution linkage mapping through power simulations and statistica

122 ptible Wistar-Furth (WF) rats as a panel for linkage mapping to genetically identify mammary carcinom

123 We use quantitative behavioral assays and linkage mapping to identify a genetic locus (nict-1) tha

124 Finer linkage mapping using a high density of microsatellite m

125 dominant transmission, and performed genetic linkage mapping using both parametric and non-parametric

126 Here we also report linkage mapping using the 690 K array, which allowed map

127 I apply the method to do qualitative trait linkage mapping using the nonparametric sharing statisti

128 the feasibility and efficacy of this form of linkage-mapping, using congenital hyperinsulinism (HI),

129 Linkage mapping was performed in 10 families.

130 Linkage mapping was performed using single-nucleotide po

131 Through linkage mapping we assign these variants to a particular

132 In this study, segregation analysis and linkage mapping were performed to localize an amphibian

133 Here, we use comparative linkage mapping with gene-based markers to reconstruct c

134 We conducted classical linkage mapping with microsatellites in a large multigen

135 Linkage mapping with reference populations failed to rev