戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 e sibling-pair cohort was subjected to finer linkage mapping.
2 f resulting progeny were analyzed by genetic linkage mapping.
3 tified, which were subsequently validated by linkage mapping.
4 agments that was not resolved by the genetic linkage mapping.
5 16 origin of clones was confirmed by genetic linkage mapping.
6  the critical region through YAC content and linkage mapping.
7  deep shotgun sequencing and high-resolution linkage mapping.
8  cannabinoid synthase genes and were used in linkage mapping.
9  and dry weight accumulation under low P via linkage mapping.
10 nd conducted both single- and combined-cross linkage mapping.
11 re rapid and cost-effective than traditional linkage mapping.
12 assisted bulk segregant analysis followed by linkage mapping.
13 lucidate regulatory networks and can improve linkage mapping.
14 eviously on the basis of comparative genetic linkage mapping.
15 d from varieties AU9 and SunUp were used for linkage mapping.
16 orin-2 (Aqp2) in cph mutants through genetic linkage mapping.
17  an average of 8.2 AFLP markers eligible for linkage mapping.
18 e use of positional cloning, which relies on linkage mapping.
19  biased estimation and reduced efficiency in linkage mapping.
20 characterized the rc phenotype and initiated linkage mapping.
21 nd suggests a new mathematical framework for 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 n kinase (Strn-Mlck), which we validate with linkage mapping and transgenic manipulation of gene expr
39 rican families with the RP10 form of adRP by linkage mapping and used these families to reduce the li
40                                              Linkage mapping and whole-exome sequencing identified ho
41                              Through genetic linkage mapping and whole-exome sequencing, we identifie
42 sed genome-wide association studies (mGWAS), linkage mapping, and heterologous expression assays, we
43 rom 55 family members (UM:H389) was used for linkage, mapping, and mutation analysis.
44                                              Linkage mapping associating dicamba injury with genotype
45 the genotype-phenotype association (based on linkage mapping, association mapping or a candidate gene
46 ds of unique recombinant progeny for genetic linkage mapping, bulk segregant analysis, and high-throu
47 able for genome-wide high-resolution genetic linkage mapping, by recurrent intermating among F2 indiv
48 n experiments, STS-based PCR assays, genetic linkage mapping, cDNA localization, and FISH data.
49     Using a unique property of multiparental linkage mapping designs, for each QTL we highlight a rel
50    Chromosome assignment of markers based on linkage mapping differed from sequence alignment with th
51                                   We perform linkage mapping, estimates of genome-wide and per-chromo
52 nd ataxia, where either clinical features or linkage mapping excluded known PME loci.
53                Through association analysis, linkage mapping, expression analysis, and mutagenesis, w
54 bridization, and all the markers assigned by linkage mapping fall within a 1.6-cM interval.
55                                              Linkage mapping finds a significant interaction effect f
56  in the presence of (E)-B-ocimene; combining linkage mapping, gene expression, and functional analyse
57                     We used a combination of linkage mapping, genome-wide association studies (GWAS),
58                               Traditionally, linkage mapping has been the most commonly employed meth
59                                        Dense linkage mapping has highlighted the presence of 2 loci o
60                                      Genetic linkage mapping has identified more than 100 plant resis
61                                              Linkage mapping has previously shown convergent red wing
62                    Genotyping, as applied to linkage mapping, human identification, or mapping of gen
63 ide association and targeted high-resolution linkage mapping identified ZmCCT, a homologue of the ric
64                                  Genome-wide linkage mapping identifies a single chromosome region at
65                                  Genome-wide linkage mapping identifies largely separate sets of quan
66     These results demonstrate the utility of linkage mapping in a human helminth parasite, while crys
67 P (adRP) was placed on chromosome 17p13.3 by linkage mapping in a large South African adRP family.
68                            Using genome-wide linkage mapping in marine-freshwater F2 genetic crosses,
69 ncertainty about linkage phases of founders, linkage mapping in nonmodel, outcrossing systems using m
70                     Statistical analyses for linkage mapping in polyploid species can be difficult du
71 t covers existing statistical approaches for linkage mapping in polyploids that are predominantly mul
72                   Here, we report the use of linkage mapping in synthetic F2 populations and compleme
73                                  Large-scale linkage mapping in the budding yeast Saccharomyces cerev
74   Family-nested QTL were identified by joint-linkage mapping in the NAM panel.
75                                              Linkage mapping in two species groups, gene-expression a
76 n this chromosome-wide reproductive barrier, linkage mapping indicates that cis-regulatory variation
77                                              Linkage mapping indicates that the modifying gene is ver
78  show that association mapping combined with linkage mapping is a powerful method to discover importa
79                         High-density genetic linkage mapping is a valuable and effective method for e
80 der of genes in genomes for which gene-based linkage mapping is impractical.
81  studies of rare diseases, the resolution of linkage mapping is limited by the number of available me
82                                    Moreover, linkage mapping is one of the best ways to detect errors
83                                  The goal of linkage mapping is to find the true order of loci from a
84 s of the crossover events and the multipoint linkage mapping localized the disease locus to an 8.8-cM
85 ing nullisomic deletion mapping with meiotic linkage mapping, loci known to be located on a particula
86                                              Linkage mapping methods have identified major-effect eQT
87 ial value of recently developed high-density linkage mapping methods in the analysis of complex disea
88        This study describes the physical and linkage mapping of 42 gene-associated markers developed
89                                    Exclusion linkage mapping of chromosome 16 was performed in a sepa
90                                              Linkage mapping of complex diseases is often followed by
91 AP-O-MAT is a web-based server for automated linkage mapping of human polymorphic DNA markers.
92                    We then performed genetic linkage mapping of male-specific traits important for re
93                                              Linkage mapping of methylation states assessed from whol
94                                              Linkage mapping of progeny surviving >15 mg/kg CQ identi
95 ased association mapping and of family based linkage mapping of quantitative traits in humans.
96 ws the challenges we face in moving from the linkage mapping of susceptibility genes for type 2 diabe
97                           Reported herein is linkage mapping of the H locus to a 3.27 Mb region of ch
98 otide polymorphism (SNP) assays designed for linkage mapping of the human genome.
99                                  We combined linkage mapping of the loci that control cyanogenesis (A
100                            We further report linkage mapping of the primary cea locus to a 3.9-cM reg
101                                      Genetic linkage mapping of two crosses showed dominance of male
102 ustrate an approach to combined physical and linkage mapping of type 1 anchor (gene) loci in the dog
103 bleomycin-response differences by performing linkage mapping on recombinants derived from a cross bet
104 ntified by whole-genome sequencing following linkage mapping or by whole-exome sequencing.
105  linkage mapping set, the Illumina BeadArray linkage mapping panel (version 3) and the Affymetrix Gen
106 is, we have genotyped the Illumina BeadArray linkage mapping panel (version 4) in a data set of 730 m
107                                              Linkage mapping placed Pafaha-ps1 and Pafaha-ps2 to dist
108                               By integrating linkage mapping, polyploid phylogeny and sex-determining
109 ii and M. cardinalis was explored in a large linkage mapping population of F2 plants n = 465 to provi
110           The implications of this model for linkage mapping, population genetic studies, and polyplo
111                                Historically, linkage mapping populations have consisted of large, ran
112 re incorporated in our new, freely available linkage-mapping program MULTIGENE 1.0 for the PC environ
113 y found specific polymorphic markers for our linkage mapping project.
114 t, a combination of correlation analysis and linkage mapping provides the potential to identify and s
115                   We selected 7,734 SNPs for linkage mapping, resulting in 27 linkage groups with a m
116                              The comparative linkage mapping results indicate that the q arm of human
117                                        Joint-linkage mapping revealed that the genetic architecture o
118                                              Linkage mapping revealed that two point mutations are re
119                                 High-density linkage mapping revealed three major-effect QTL distribu
120 nt microsatellite markers from the ABI Prism linkage mapping set v.2 on an ABI 377 sequencer/genotype
121       For the microsatellites, the ABI Prism Linkage Mapping Set version 2, with 402 microsatellite m
122 ted relatives per family using the ABI Prism linkage mapping set which includes 350 polymorphic marke
123 plied Biosystems high-density microsatellite linkage mapping set, the Illumina BeadArray linkage mapp
124 n an Applied Biosystems model 377 (ABI PRISM Linkage Mapping Sets; Perkin Elmer Applied Biosystems),
125                                              Linkage mapping showed that body weight (BW) loci on pro
126                                  Genome-wide linkage mapping shows that pelvic reduction is controlle
127                            Here we present a linkage mapping software Lep-MAP3, capable of mapping hi
128                                              Linkage mapping studies in model organisms have typicall
129 duced and form a unique resource for genetic linkage mapping studies in the horse.
130 e results demonstrate the benefits for horse linkage mapping studies of genotyping on these unique fu
131 ted genetic maps can have adverse effects on linkage mapping studies.
132 bined fluorescence in situ hybridization and linkage mapping, the gene order on CFA9 is similar to th
133                                           By linkage mapping, the transgene integration site was loca
134 the utility of these data in high-resolution linkage mapping through power simulations and statistica
135 d by genomic approaches ranging from genetic linkage mapping to analysis of gene regulation.
136 hromosomes and use sequencing, Hi-C(3,4) and linkage mapping to assemble a chromosome-scale genome re
137 ptible Wistar-Furth (WF) rats as a panel for linkage mapping to genetically identify mammary carcinom
138    We use quantitative behavioral assays and linkage mapping to identify a genetic locus (nict-1) tha
139                                        Finer linkage mapping using a high density of microsatellite m
140 dominant transmission, and performed genetic linkage mapping using both parametric and non-parametric
141                          Here we also report linkage mapping using the 690 K array, which allowed map
142   I apply the method to do qualitative trait linkage mapping using the nonparametric sharing statisti
143 the feasibility and efficacy of this form of linkage-mapping, using congenital hyperinsulinism (HI),
144                                              Linkage mapping was performed in 10 families.
145                                              Linkage mapping was performed using single-nucleotide po
146                                      Through linkage mapping we assign these variants to a particular
147                            Using large-scale linkage mapping, we discovered a novel defense factor, w
148 tal and phenotypic association analyses with linkage mapping, we identified genes linking environment
149            Combining population genetics and linkage mapping, we identify a number of regions/genes p
150      In this study, segregation analysis and linkage mapping were performed to localize an amphibian
151 ying the genetic basis of trait variation is linkage mapping, which identifies quantitative trait loc
152                     Here, we use comparative linkage mapping with gene-based markers to reconstruct c
153                            Here, we combined linkage mapping with genome scans to identify High Phosp
154                       We conducted classical linkage mapping with microsatellites in a large multigen
155                                              Linkage mapping with reference populations failed to rev
156                                              Linkage mapping yielded candidate loci on chromosomes II

 
Page Top