| genome-wide association study (GWAS) |
was conducted to |
map genetic variants associated with virulence to Pm1a |
Blumeria graminis |
| causal locus |
was narrowed down to |
348-kb region between markers S21 and S52 |
Zea mays |
| HORVU5Hr1G089230 |
is |
candidate for CER-ZA |
Hordeum vulgare |
| HORVU4Hr1G063420 |
was previously identified as |
gene underlying the cer-zh.54 mutation |
Hordeum vulgare |
| regulator BSA |
identified |
QTL for flower color at beginning of Scaffold 16 |
Amaranthus hypochondriacus |
| F2 population |
was genotyped using |
GBS (genotyping-by-sequencing) |
Capsicum annuum |
| QTL analysis of F2 population |
revealed |
57 QTLs controlling flavonoid content |
Capsicum annuum |
| two BSAs from different initial crosses |
were conducted to |
study genetic basis of tissue color and its regulation |
Amaranthus hypochondriacus |
| genome-wide association study (GWAS) |
analyzed |
216 (BGT, GCN5, HAC3, HAG01, HAG1, HAT1, AT3G54610) isolates from six countries |
Blumeria graminis f. sp. tritici |
| QTL-seq |
is |
BSA-seq |
|
| Mu insertion |
co-segregates with |
dek58 phenotype |
Zea mays |
| crumpled kernel mutant (crk2) |
was introgressed into |
inbred line ZI819 background |
Zea mays |
| genome-wide association study (GWAS) |
was conducted in |
216 (BGT, GCN5, HAC3, HAG01, HAG1, HAT1, AT3G54610) isolates from six countries |
Blumeria graminis |
| lincRNA identified as potentially related to a trait |
was identified if SNP was found either within |
lincRNA locus |
Glycine max |
| PCR-amplified genomic DNA |
was sequenced to identify |
the mutation |
Arabidopsis thaliana |
| af |
has only two recombination events between |
PsCam023334_13180_1532 |
Pisum sativum |
| NILs (F6) |
were constructed to differ at |
QTL marker alleles |
Capsicum annuum |
| af |
has ten recombination events between |
PsCam000001_1_322 |
Pisum sativum |
| variation in C4 traits within a single species |
is not known to be sufficient for |
breeding and molecular trait mapping |
|
| interaction between lincRNA and neighboring protein-coding gene |
is also possible |
in contributing to trait |
Glycine max |
| 18X-551 S2 family linkage map |
includes |
423 individuals and 1019 markers across 23 linkage groups |
Salix purpurea |
| genetic markers |
are |
DNA sequences with known chromosomal positions |
|
| af |
is genetically closer to |
PsCam023334_13180_1532 |
Pisum sativum |
| debino1 mutation |
is mapped to |
upper arm of Chromosome 6 |
Medicago truncatula |
| parallel approach |
identified |
close linkage between af and PsCam002050 |
Pisum sativum |
| simple sequence repeat (SSR) |
is also known as |
microsatellites |
|
| genome-wide association study (GWAS) |
led to the discovery of |
second locus that also conditions (BGT, GCN5, HAC3, HAG01, HAG1, HAT1, AT3G54610) virulence to wheat resistance gene Pm1a |
Blumeria graminis; Triticum aestivum |
| Genotyping the recombinant lines from (GABA-T, HER1, POP2, AT3G22200) (POP4, AT2G43190) (AtPOP5, EMB1687, POP5, AT1G04635) and BxP at the af locus |
confirmed the co-segregation of |
PsPALM1a, PsPALM1b and PsNAOD1 with Af |
Pisum sativum |
| handful of SNPs |
remain significantly associated with |
circularity, oPC1, iPC3, and iPC2 |
Vitis spp. |
| ~70-kb region between F26G16-a and T5I8-d markers |
contains |
20 annotated genes |
Arabidopsis thaliana |
| comparison of allele frequencies between bulks |
identified |
large QTL on Scaffold 16 |
Amaranthus hypochondriacus |
| GWAS of low water potential-induced Pro accumulation coupled with phenotyping of transfer DNA (T-DNA) insertion mutants and overexpression lines |
was conducted |
to evaluate heuristic methods for scoring and prioritizing candidate genes for subsequent validation |
Arabidopsis thaliana |
| several loci typically found in vicinity of trait associated SNP |
makes it usually not immediately obvious which one may contribute to |
trait |
Glycine max |
| data from Castelporziano and Rht18 analysis |
support |
hypothesis that Rht14 and Rht18 are allelic |
|
| P23F12 mutation |
maps to |
chromosome 9 |
Solanum lycopersicum |
| (AtSAMS3, MAT4, MTO3, SAMS3, AT3G17390) locus |
was narrowed to a region between |
bacterial artificial chromosome clones K14A17 and (ATMAPK6, ATMPK6, MAPK6, MPK6, AT2G43790) on chromosome 3 |
Arabidopsis thaliana |
| genome-wide association (GWAS) |
localizes associations to |
much smaller genomic regions |
Arabidopsis thaliana |
| Ceratadon purpureus |
is the subject of |
genetic mapping project |
Ceratadon purpureus |
| high heritability of our traits |
suggests that |
further development of genotyping resources and sufficiently powered GWAS studies may resolve loci regulating leaf shape |
Vitis spp. |
| mean genic and genic plus promoter P values |
effective in finding |
promising candidate genes |
Arabidopsis thaliana |
| GWAS analysis of tissue cadmium content |
found |
single strong genome-wide association (GWAS) peak |
|
| (AtSAMS3, MAT4, MTO3, SAMS3, AT3G17390) mutant |
was crossed with |
wild-type L er |
Arabidopsis thaliana |
| F1 plants from the cross |
were self-fertilized to produce |
F2 seeds |
Arabidopsis thaliana |
| neutral mutant |
is crossed with |
spontaneous mutant |
Oryza sativa |
| F2 populations derived from 3t mutant and neutral mutant EMS-ZH11 |
shared almost the same genetic background as |
ZH11 |
Oryza sativa |
| 20 linkage groups |
correspond to |
20 chromosomes |
Glycine max |
| 1189 SNPs with unique linkage map positions |
versus |
16650 total SNPs mapped |
Pennisetum glaucum |
| analyses of genotypic data from numerous RIL populations |
showed that all polymorphic SNPs were clustered into |
20 linkage groups |
Glycine max |
| six of the lincRNAs |
overlapped |
trait-associated SNPs |
Glycine max |
| GWA analysis |
identified |
2,382 genes associated with lesion size |
Arabidopsis thaliana |
| genome-wide association study (GWAS) |
was performed for |
our traits |
Vitis spp. |
| quantitative trait locus (QTL) mapping and genome-wide association (GWAS) |
cannot by themselves prove |
causality |
|
| thioredoxin genes |
contained in |
regions 15 and 47 |
Arabidopsis thaliana |
| (ACC2, AT1G36180) and suppressor |
show perfect linkage |
genetic distance less than 1 centimorgan |
Arabidopsis thaliana |
| 110 plants of interest |
were genotyped using PCR primers for |
(EMB3137, uS13c, AT5G14320) (ATOEP80, EMB213, OEP80, TOC75-V, AT5G19620) and (ATTOC34, OEP34, TOC34, AT5G05000) |
Arabidopsis thaliana |
| straightforward methods of sorting and ranking SNP data |
can increase |
the information that can be extracted from GWAS |
|
| nonsignificant single-nucleotide polymorphisms in gene body or promoter |
penalize mean genic and genic plus promoter P values |
mean genic and genic plus promoter P values |
Arabidopsis thaliana |
| distribution of genome-wide association (GWAS) signal among many genomic regions |
would seem to differ from |
GWAS results for secondary metabolites and amino acids |
|
| genome-wide association (GWAS) |
generally combines |
phenotype and single-nucleotide polymorphism (SNP) data from 100 or more accessions |
Arabidopsis thaliana |
| strong phenotype-SNP associations |
have been found for |
candidate genes identified a priori from molecular genetic studies |
Arabidopsis thaliana |
| chy1-10 mutant |
was crossed with |
wild-type plants of the L er ecotype |
Arabidopsis thaliana |
| 33 simple sequence repeat (SSR) markers |
narrowed male sterility gene to |
candidate region between NAU3442 and CGR6339 |
Gossypium hirsutum |
| segregation analysis |
allowed mapping of |
genes |
Oryza sativa |
| 23 lincRNA candidates |
have been identified |
as potentially trait-related |
Glycine max |
| QTL studies |
typically use |
two or at most several parental accessions |
Arabidopsis thaliana |
| GWA analysis |
identified |
4,110 genes associated with lesion greenness |
Arabidopsis thaliana |
| association signal around true causal polymorphisms |
could vary in strength and genomic pattern for |
a large number of reasons including effect size, mutation age, recombination pattern, and linkage disequilibrium |
|
| interaction between genes |
can influence |
strength of association detected in genome-wide association (GWAS) |
|
| GWA analysis |
identified |
1,933 genes associated with lesion eccentricity |
Arabidopsis thaliana |
| genomic DNA corresponding to candidate genes |
was PCR-amplified from |
mutant and wild-type plants |
Arabidopsis thaliana |
| genome-wide association (GWAS) |
identifies |
loci with allele frequency correlations to phenotypic variation or environment |
Arabidopsis thaliana |
| The absence of segregation for incompatibility |
confirmed that |
sulki1 mutants are allelic to Cas9-r8 |
Arabidopsis thaliana |
| GWAS mapping |
was performed using |
288 Arabidopsis accessions distributed worldwide |
Arabidopsis thaliana |
| genome-wide association studies |
have been successful in |
uncovering genetic basis of trait variation and linking causal loci to phenotypic traits |
|
| GWAS applied to association panel accounting for kinship |
screened |
10 genomic regions captured within 11 QTLs |
Zea mays |
| GWAS |
is |
a relatively new approach |
|
| remaining intergenic trait-associated variants |
can potentially be assigned to |
lincRNAs |
Glycine max |
| 316 single-nucleotide polymorphisms identified as associated with agronomic traits |
were used in |
analysis |
Glycine max |
| map location of Rht24 |
overlapped |
Rht18 region on chromosome 6A that included GA2oxA9 |
|
| F2 segregating population derived from 3t mutant and Zhenshan 97 (ZS97) |
was constructed from |
3t mutant and indica cultivar Zhenshan 97 (ZS97) |
Oryza sativa |
| genes showing chromosomal locations corresponding to known disease resistance QTLs |
are identified by |
bioinformatics analysis |
Oryza sativa |
| CER-ZA |
is likely |
HORVU5Hr1G089230 |
Hordeum vulgare |
| molecular markers |
are used for |
construction of genetic linkage maps |
|
| 48 SNPs in BARCSoySNP6K assay |
have genetic location not inferred because |
physical positions in Wm82a2v1 soybean assembly not determined |
Glycine max |
| Phenotyping and genotyping of Thellungiella ecotype collections |
will provide essential resource for |
gene identification by QTL analysis and mutant mapping |
|
| genomic DNA extracted from seedlings |
was used for |
PCR-based mapping |
Arabidopsis thaliana |
| ced2 mutation |
is mapped to |
128-kb interval on chromosome 3 |
Arabidopsis thaliana |
| F20D10 primer |
is used for |
mapping |
Arabidopsis thaliana |
| 3231 markers with unique genotypic profiles |
versus |
2077 markers that co-segregated with one of the 3231 SNPs |
Glycine max |
| markers with significant segregation distortion |
were discarded from |
mapping data |
|
| all polymorphic SNPs clustered into 20 linkage groups |
suggests that SNPs well cover |
soybean genome |
Glycine max |
| RIL population from cross between tomato and S. pimpinellifolium |
was profiled using |
genome wide SNP analysis |
Solanum lycopersicum; Solanum pimpinellifolium |
| genotypes of F2 individuals |
cosegregated with |
tiller number |
Oryza sativa |
| limited number of recombination events (REs) |
suggests that |
for a biparental population with a limited number of recombinant inbred lines (RILs), it is unnecessary to genotype the RILs with too many markers |
|
| Solanum lycopersicum cv M82 |
crossed with |
Solanum pennellii |
Solanum lycopersicum; Solanum pennellii |
| SSLP and CAPS markers |
were employed to |
localize fsh mutation on chromosome 1 |
Arabidopsis thaliana |
| 12K SNP array analysis of RP6Ht3 |
revealed segments differing from RP6 on |
chromosomes 2, 3, 4 and 8 |
Zea mays |
| 69 QTLs for plasticity traits across the two populations |
about 78% were detected only when using |
the plasticity index |
|
| Medea Ap9d |
was null for |
Sr13 |
Triticum aestivum |
| Srdp2 |
is not |
allele of Sr13 |
Triticum aestivum |
| CAT-A1 |
was derived from |
Camadi Abdu tipo #103 (PI 192168) |
Triticum turgidum |
| 22 additional durum wheats |
were added to |
analysis for validation of rwgsnp38, rwgsnp39 and rwgsnp40 |
Triticum turgidum |
| low limit of detection (LOD) scores for some QTL |
are reflective of |
whole genome average interval mapping (WGAIM) method |
Hordeum vulgare |
| WGAIM method |
detects and quantifies |
smaller effect QTL |
Hordeum vulgare |
| many QTL |
were transient and only appeared at |
individual time points |
Hordeum vulgare |
| QTL on chromosome 1H |
was not detected for |
any of PSA-related traits |
Hordeum vulgare |
| genetic variation at regionally polymorphic causal loci |
might be insufficient within |
a given local population |
|
| putative centromeric regions |
were identified using |
recombination rate variation along eight LGs |
Marchantia polymorpha |
| recombinationally inactive regions |
were located close to |
middle or close to one end of pseudomolecules |
Marchantia polymorpha |
| substantial genome portions uncovered |
renders opaque to |
further genetic profiling |
|
| fsh mutation |
is localized between |
markers sup4.04 and PERL0029221 |
Arabidopsis thaliana |
| Marey maps |
indicated |
recombination rate variation along eight pseudomolecules deviated significantly from zero |
Marchantia polymorpha |
| statistical methods combining trait values and allelic variation in segregant populations |
characterize |
quantitative trait loci (QTLs) |
Zea mays |
| AP22 primer |
is used for |
mapping |
Arabidopsis thaliana |
| recombinationally active and inactive regions |
were used to identify |
putative centromeric regions |
Marchantia polymorpha |
| LG1, LG2, LG4, LG5, and LG6 |
showed |
one major extensive region with very low recombination rate |
Marchantia polymorpha |
| allele frequency |
is calculated between |
mutant pool and neutral mutant |
Oryza sativa |
| quantitative trait locus (QTL) mapping using 38 polymorphic markers in a BC2F2 population |
detected |
single association peak with LOD value of 44.02 at physical position 158.17 Mb |
Zea mays |
| QTL mapping |
is method for characterizing |
quantitative trait loci (QTLs) |
Zea mays |
| genome-wide association study of 84 traits using 809 accessions |
demonstrated that |
at least 23 loci with pleiotropic effects on different traits |
Glycine max |
| 2,862 SNPs in BARCSoySNP6K assay |
had genetic position inferred for |
SNPs not mapped in WP linkage map |
Glycine max |
| leaf length |
resulted in |
nine MTAs |
Zea mays |
| genes in the 2.1-Mb candidate interval |
possess |
pivotal variations |
Gossypium hirsutum; Gossypium barbadense |
| all three plants of CAT-A1 |
were positive for |
Sr13 |
Triticum turgidum |
| Two of the annotated genes (unknown function; ABC transporter G family member) |
making unlikely candidates for |
salt responsive leaf elongation QTL at vegetative growth |
Hordeum vulgare |
| genetic resources |
are used for |
quantitative trait analysis |
Arabidopsis thaliana |
| panels of genotypes |
provide |
high genetic resolution based on historical recombination events |
|
| neutral mutant EMS-9311 |
was selected for crossing with |
srl mutant |
Oryza sativa |
| OF2 |
was determined to be located on |
chromosome A09 between markers APSP63 and ANP41 |
Brassica napus |
| syl mutation locus |
defined by interval between |
markers nga 225 and nga 249 |
|
| ssd3-1 to ssd3-7 alleles |
are |
third complementation group |
Arabidopsis thaliana |
| Spr3 |
is narrowed down to |
4.6-kb region |
Oryza sativa |
| CsTW5.1 |
was overlapping to |
non-significant QTL of CsFW |
Arabidopsis thaliana |
| linkage analysis |
obtained |
thirteen linkage groups |
Ficus erecta |
| neutral mutant-bridging (NMB) method |
was developed for |
mapping the naturally mutated gene |
Oryza sativa |
| genotypes at peak SNP site on chromosome 12 |
were not cosegregated with |
phenotype of tiller number |
Oryza sativa |
| BARCSoySNP6K assay |
has been used to construct |
linkage maps |
Glycine max |
| genome-wide association study (GWAS) on grain (1,3;1,4)-β-glucan content |
confirmed |
QTL on 1H co-locating with HvCslF9 and HvGlbI |
Hordeum vulgare L. |
| 4-day-old etiolated F2 seedlings with enhanced ethylene response phenotype |
used for |
collection of leaf tissue and isolation of genomic DNA |
Arabidopsis thaliana |
| introgression line (IL) population |
contains |
introgressed segments from Solanum pennellii |
Solanum lycopersicum; Solanum pennellii |
| neutral mutant crossed with spontaneous mutant |
develops |
pseudo-near-isogenic F2 population |
Oryza sativa |
| next generation mapping |
used to identify |
mutated locus in each plant line |
Arabidopsis thaliana |
| neutral mutant crossed with spontaneous mutant |
develops |
F2 population |
Oryza sativa |
| bulked segregant analysis |
mapped |
(GIR1, AT5G06270) gene |
Arabidopsis thaliana |
| position of centromeres |
could be readily defined for |
LG1, LG2, LG3–LG6 |
Marchantia polymorpha |
| mapping to a single locus in F2 populations |
argues for |
single gene basis |
Zea mays |
| metabolic quantitative trait locus (mQTL) mapping |
is |
powerful tool for the identification of genetic determinants of plant metabolism |
|
| SNPs in BARCSoySNP6K assay |
are all linked to |
one of 20 linkage groups |
Glycine max |
| SNPs |
were grouped into |
12 linkage groups |
|
| large-scale genetic studies, including GWAS and linkage mapping |
can identify |
new genes and alleles that regulate the plant ionome |
Arabidopsis thaliana |
| maize studies |
benefit from |
advanced segregant populations |
Zea mays |
| two RIL sets used as a combined mapping panel |
can result in |
discrepancies among gene lists |
Zea mays |
| 14 pairs of paralogs in candidate intervals |
were initially found |
in candidate intervals |
Gossypium hirsutum |
| marker rwgsnp40 |
was developed to detect |
plants carrying haplotype R1 |
Triticum aestivum; Triticum turgidum |
| Rusty-14803, PI 387696 and Im-C2 |
had |
R2 haplotype |
Triticum turgidum; Triticum carthlicum |
| R4 haplotype |
differed from R2 by only |
1 bp at C2798A/T933K |
Triticum turgidum |
| observation of a given causal variant on different haplotypes in different geographic regions |
breaks down |
correlations in genotype between the causal variant and nearby non-causal variants |
|
| order of markers on linkage maps constructed with BARCSoySNP6K |
is consistent with |
order of markers on linkage maps constructed with SoySNP50K |
Glycine max |
| consensus map |
contains |
12 linkage groups |
|
| root mean squared error between maps |
had maximum of |
5.75 on LG 5 |
|
| QTL mapping using 720 BC2F2 plants |
found single association peak with LOD value of 168.77 at |
position 158.17 Mb on chromosome 8 |
Zea mays |
| genotyping-by-sequencing |
mapped |
genetic locus CaOr on chromosome 2 |
Capsicum annuum |
| genetic determinism of seed protein composition |
is likely mainly dependent on |
environment |
Medicago truncatula |
| monogenic line CAT-A1 |
was found to carry |
new haplotype, named R4 |
Triticum turgidum |
| all monogenic lines except CAT-B1 |
carried |
Sr13 haplotype |
Triticum turgidum; Triticum aestivum |
| regions with lowest and most extensive recombination suppression |
were identified as |
putative centromeres |
Marchantia polymorpha |
| linkage map |
corresponds to |
eight autosomes |
Marchantia polymorpha |
| low REs in plant genomes |
suggests that genotyping RIL populations of limited sizes with large number of markers is unnecessary |
high LD in RIL populations |
|
| two SNPs from PILA_30024 gene |
were located at |
position 59.81 cM of LG 7 |
|
| introgression line (IL) population |
covers |
full Solanum pennellii genome |
Solanum lycopersicum; Solanum pennellii |
| 0.3 cM genetic interval flanked by markers PZE-108096469 and PZE-108092843 |
flanks |
2.81 Mb region on chromosome 8 of (B73, CHL6, CNX, CNX1, SIR4, AT5G20990) reference genome |
Zea mays |
| all polymorphic InDels (28 pairs) |
exhibited linkage phenomenon with |
male sterility |
Gossypium hirsutum; Gossypium barbadense |
| multi-parental mapping populations |
overcome limitations of |
biparental mapping populations |
|
| locus L5 |
is located at |
chromosome 5 at approximately 16.5 Mb |
Arabidopsis thaliana |
| spatial correction |
was implemented for |
GWAS on raw phenotypic data according to a randomized split-plot block design |
Arabidopsis thaliana |
| SNP linkage map |
mapped |
genetic position of orange fruit color locus |
|
| genetic linkage groups |
had average marker density of |
1.5 cM/marker |
Triticum aestivum; Triticum carthlicum |
| CAT-A1 |
carried |
T2200C polymorphism |
Triticum turgidum |
| QTL on chromosome 1H for total.length.smooth (117.22–119.78 cM) under salt at 24 DAP |
shares flanking marker with |
QTL at 119.78 cM for mean.length.smooth under control conditions |
Hordeum vulgare |
| recombinant inbred lines |
is |
bi-parental mapping population |
|
| local populations |
are not without |
limitations |
|
| late TT and early TT plants from Tsu-0 × emb3126-1 crosses |
were genotyped using |
PCR primers revealing accession-specific DNA sequence polymorphisms |
Arabidopsis thaliana |
| GWA analysis |
identified |
4,383 genes associated with lesion yellowness |
Arabidopsis thaliana |
| GWA and eQTL mapping |
used |
covariate and kinship correction |
Zea mays |
| highly efficient populations for QTL mapping |
represent |
alternatives for characterizing other heat-response QTLs |
Solanum lycopersicum |
| many QTLs identified |
were |
condition-specific suggesting that, depending on the condition, the effect of QTLs significantly varied |
|
| previous QTL mapping studies on tomato response to high temperature |
were conducted on |
traits evaluated in a single HS condition |
|
| hotspots for both plasticity and protein band abundance |
identified on |
chromosome 1 (at approx. 50 Mb) and chromosome 2 |
Medicago truncatula |
| 1542 polymorphic SNP markers |
were used for |
genetic map construction |
Triticum aestivum; Triticum carthlicum |
| genetic linkage groups |
had total map length of |
2356.5 cM |
Triticum aestivum; Triticum carthlicum |
| false positives from markers rwgsnp38, -39 and -40 |
are easily detected by |
rwgsnp37.2 |
Triticum aestivum |
| QTL for num.leaves on chromosome 5H between 51.83 and 56.80 cM |
such as |
QTL specific to leaf number |
Hordeum vulgare |
| GWASs and QTL mapping |
are |
most common and effective methods used to analyze agronomically important plant characters |
|
| genetic interval 6.06–6.43 Mb on chromosome 7 |
encompasses |
seven distinct linkage disequilibrium (LD) blocks |
Oryza sativa |
| 14 pairs of paralogous genes |
were identified based on |
two mapping regions |
Gossypium hirsutum; Gossypium barbadense |
| resistant seedling CHC543-5 × susceptible seedling CHC544-5 |
generated |
F1 population 7650 |
Solanum chacoense |
| marker TG63 |
linked to |
Rpi-chc1 resistance |
Solanum chacoense |
| distribution of hotspots throughout genetic map |
reflects |
complex genetic determinism of seed protein composition |
Medicago truncatula |
| 1621 polymorphic markers |
were assigned to |
14 linkage groups representing 14 (A and B genomes) chromosomes |
Triticum aestivum; Triticum carthlicum |
| remaining three candidates underlying QTL |
included |
two expansin B2 genes and glucan endo-1,3-beta-glucosidase |
Hordeum vulgare |
| genome-wide association studies (GWAS) |
uncover collections of loci that are far from exhaustive |
loci associated with trait variation |
|
| isolation of induced mutations in (ATPAD4, PAD4, AT3G52430) after mutagenesis of syp121–1 syp122–1 |
overcame |
genetic linkage barrier |
Arabidopsis thaliana |
| L4204 marker |
is |
CAPS marker type |
Oryza sativa |
| L4359 marker |
is |
Indel marker type |
Oryza sativa |
| 200 plants selected from F2 population |
genotyped and phenotyped for |
linkage map construction and linkage analysis |
Oryza sativa L. |
| F6G17 primer |
is used for |
mapping |
Arabidopsis thaliana |
| neutral mutant EMS-9311 crossed with srl mutant |
developed |
another F2 population |
Oryza sativa |
| LD decay information |
was used to reduce redundancy between |
MTAs in linkage with each other |
Zea mays |
| several QTLs of the present study |
were consistent with |
their results, for flower, fruit number or fruit set (on chromosomes 2, 4, 5, 6, 7, 10 and 12) |
|
| polymorphic SNP markers |
were co-segregating |
co-segregating marker sets |
Triticum aestivum; Triticum carthlicum |
| R4 haplotype |
differed from R3 by only |
1 bp at G2517T/W839C |
Triticum turgidum |
| only 6 of 15 Camadi plants |
carried |
R4 haplotype |
Triticum turgidum |
| Camadi plants #1 and #3 |
were both positive for |
Sr13 marker rwgsnp37.2 |
Triticum turgidum |
| significant QTL for PSA.smooth.RGR |
is in close proximity |
33.43–33.62 cM |
Hordeum vulgare |
| both QTL |
each accounting for approximately |
5% of genetic variation |
Hordeum vulgare |
| Chromosome 3H |
detected |
QTL region specific to salinity response for leaf length-related traits |
Hordeum vulgare |
| Four traits (total.length.smooth, total.length.smooth.AGR, L4.length.smooth and num.leaves) |
were mapped between |
67.56 and 69.50 cM |
Hordeum vulgare |
| QTL specific to length of leaf 4 |
analyzed |
QTL with highest LOD score (6.5) on chromosome 3H |
Hordeum vulgare |
| linkage mapping populations |
can be used to |
identify quantitative trait loci (QTL) |
|
| rough mapping interval |
is screened for |
recombinants |
|
| discrete linkage disequilibrium blocks |
delimit |
R gene |
|
| DZ size |
was associated with loci on |
chromosome (Chr) 1 at around 175 Mb |
Zea mays |
| high proportion of population-specific QTLs for fruit- and plant-related traits under optimal growth conditions |
was observed in |
Pascual et al . ( 2016 ) |
|
| Δ(all index) strategy |
anchored male sterility locus to |
interval from 7 040 418 to 39 545 755 bp on chromosome D12 |
Gossypium hirsutum |
| candidate interval |
was narrowed down to |
approximately 15.9-Mb region between A12_1156 and A12_1305 |
Gossypium hirsutum; Gossypium barbadense |
| marker rwgsnp39 |
was developed to detect |
plants carrying haplotype R3 |
Triticum aestivum; Triticum turgidum |
| 25 common wheat cultivars/lines |
had both |
Rusty and PI 387696 alleles (A1A2) |
Triticum aestivum |
| Mundah allele |
having positive effect on |
shoot growth |
Hordeum vulgare |
| association genetics |
can be based on |
panels of genotypes |
|
| local populations |
fall in between |
simplified synthetic populations and diverse global populations |
|
| effects mapped in a given local population |
may be weakened in |
other populations |
|
| at the genetic level, heat-response QTLs |
were mostly |
population specific |
|
| polymorphic 9 SSRs and 18 InDels |
were used to genotype |
F2 individuals (940, p IV) of CCRI9106 × Hai7124 |
Gossypium hirsutum; Gossypium barbadense |
| genetic map |
spanned |
total genetic distance of 1450.28 cM |
Camellia sinensis |
| 164 genes |
identified from |
plasticity indices and protein abundance |
Medicago truncatula |
| QTL for L4.length.smooth under control at 21 DAP |
had negative effect |
with allele for increased leaf 4 length coming from Keel |
Hordeum vulgare |
| candidate genes |
making interesting targets for |
future studies into salt-specific growth responses |
Hordeum vulgare |
| VRN3 mapping to (ATFT1, ATFUT1, FT1, FUT1, MUR2, AT2G03220) sequence |
suggests |
(ATFT1, ATFUT1, FT1, FUT1, MUR2, AT2G03220) is the VRN3 gene |
temperate cereals |
| whole-genome sequencing-based bulked segregant analysis (BSA) |
was performed using |
F2 population of CCRI9106 × TM-1 |
Gossypium hirsutum |
| associations on chromosomes 4 and 5 |
were found only using |
environment-specific MTMM models |
Arabidopsis thaliana |
| resistance gene in CItr 14803 |
was located at |
Sr13 locus |
Triticum polonicum |
| greater number of QTL |
was detected under |
salinity compared with control conditions |
Hordeum vulgare |
| chromosome 7H, between 177.93 cM and 180.42 cM |
detected |
two adjacent QTL for PSA.smooth.RGR |
Hordeum vulgare |
| mapping populations |
have been used in |
Arabidopsis thaliana |
Arabidopsis thaliana |
| awn traits |
mapped to |
naturally-occurring alleles in Awn-1 (An-1) and LONG AND BARBED AWN1 (LABA1) genes |
Oryza sativa |
| genetic map |
consisted of |
12 748 SNP loci in 675 genetic bins covering 705.5 cM |
Ficus erecta |
| OF1 |
was fine-mapped to |
25-kb genomic region between markers CN4/CN27 and CN36/CN40 |
Brassica napus |
| 74 simple sequence repeats (SSRs) |
were included in |
linkage map construction |
Triticum aestivum; Triticum carthlicum |
| genetic mapping using offspring from an experimental cross |
interrogates only |
genetic variants present in the parents |
|
| (ELL1, FK, HYD2, AT3G52940) mutant |
crossed with |
Nanjing 6 (NJ6) |
Oryza sativa |
| dupw167 locus |
had 259 and 296 bp amplicons from CItr 14803 assigned as |
allele B |
Triticum polonicum; Triticum aestivum |
| Rusty-KL-B and Rusty-KL-C |
had |
R1 haplotype |
Triticum turgidum |
| all three genes |
were expressed in |
seedlings |
Hordeum vulgare |
| genetic bases of natural variation |
analyzed using |
association (LD) mapping |
Arabidopsis thaliana |
| Synthetic mapping populations |
are limited to |
genetic variation present in the parental lines |
|
| local populations |
are especially effective for |
using GWAS to quantify fitness effects of causal variants in different years or habitats |
|
| nine and eight loci |
located on all chromosomes except chromosome 4 |
chromosomes 1, 2, 3, and 5 |
Arabidopsis thaliana |
| SNP markers |
enabled mapping of |
25 QTLs |
Solanum lycopersicum |
| quantitative trait locus (QTL) analysis |
performed on |
fertility phenotype |
Arabidopsis thaliana |
| cytochrome P450 superfamily protein |
making unlikely candidate for |
salt responsive leaf elongation QTL at vegetative growth |
Hordeum vulgare |
| marker |
is in strong linkage disequilibrium with |
causal variant |
|
| local populations |
suffer less from |
drawbacks of diverse natural populations and synthetic populations |
|
| fine mapping approaches to infer putatively causal variants within GWAS peaks |
achieved tighter resolution with |
a human mapping panel distributed more broadly and evenly across the globe |
|
| genotypic and phenotypic characterization |
reduces |
mapping interval |
|
| pQTLs |
from 1 to 479 genes were listed per |
QTL |
|
| association between QY max and SNPs on chromosome 5 |
was specific to |
salt stress |
Arabidopsis thaliana |
| significantly associated SNPs using Fv'/Fm' |
were distributed along |
the promoter region of (AT1G64270) and (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
Arabidopsis thaliana |
| marker dupw167 |
was |
co-dominant marker |
Triticum polonicum; Triticum aestivum |
| forward genetic approaches |
aim to associate |
mutations with traits of interest |
|
| broad mapping panels |
will yield |
higher predictive performance on average across populations |
|
| PI 387696 and newly derived near-isogenic line (NIL) Rusty-14803 |
were added to |
CNL13 sequence analysis |
Triticum turgidum; Triticum aestivum |
| sequencing results |
agreed with |
results from haplotyping |
Triticum turgidum |
| marker rwgsnp6 |
amplified |
Rusty allele (A1) in three durum and one common wheat cultivars/lines |
Triticum turgidum; Triticum aestivum |
| doubled haploid |
is |
bi-parental mapping population |
|
| GWA study |
identified |
MTAs |
Zea mays |
| approximately 15.9-Mb region between A12_1156 and A12_1305 |
contained |
138 genes |
Gossypium barbadense |
| MAGIC population |
is derived from |
intercross between four cherry and four large fruited tomato accessions |
Solanum lycopersicum |
| Ic 3 (Interval at centromeric region of chromosome 3) |
is defined by |
InDel3039 and SNP6 markers |
Hordeum vulgare |
| Rusty-14803, PI 387696 and Leeds |
all carried |
R2 haplotype |
Triticum aestivum; Triticum turgidum |
| QTL for L4.length.smooth under control at 21 DAP |
was also mapped to |
33.43 cM on chromosome 2H |
Hordeum vulgare |
| QTL for total.length.smooth on chromosome 2HL at 9.13 cM |
such as |
QTL specific to leaf length |
Hordeum vulgare |
| residual phenotype |
can be used in |
genome-wide association studies (GWAS) |
|
| genes known to alter brace roots |
are candidates for |
QTL studies |
Zea mays; Sorghum bicolor |
| studies of local populations individually |
may be |
more powerful and accurate alternative |
|
| Marchantia polymorpha linkage map |
compares well with |
linkage map of Physcomitrella patens |
Marchantia polymorpha; Physcomitrella patens |
| 3600 markers |
will be enough to |
tag each recombinant in the population |
Glycine max |
| Punnuri et al. GBS study in pearl millet |
mapped |
16650 SNPs |
Pennisetum glaucum |
| quantitative trait loci approach on recombinant inbred line progeny of Bay-0 and Shahdara cross |
identified |
six distinct quantitative trait loci |
Arabidopsis thaliana |
| L4121 marker |
is |
Indel marker type |
Oryza sativa |
| L4315 marker |
is |
CAPS marker type |
Oryza sativa |
| homozygous for Wuyujing-7 chromosomal segment plants |
selected as |
controls |
Oryza sativa L. |
| Md-PG1 |
has been genetically mapped by |
single nucleotide polymorphism (SNP) |
Malus domestica |
| two larger F2 populations, CCRI9106 × Hai7124 (p V) and CCRI9106 × 3-79 (p VI) |
were constructed to fine map |
sterility gene on chromosome A12 |
Gossypium hirsutum; Gossypium barbadense |
| genotyped panel |
can be repeatedly phenotyped to |
map new genes |
|
| male sterility genes |
were mapped on |
homologous chromosomes A12 and D12 |
Gossypium hirsutum |
| KASPSr13 marker |
co-segregated with |
Sr13 markers BE403950 and CK20734 |
Triticum aestivum; Triticum carthlicum |
| of 15 Camadi plants |
only six were positive for |
Sr13 |
Triticum turgidum |
| two adjacent QTL for PSA.smooth.RGR |
detected for |
22–23, 23–24 and 21–24 DAP |
Hordeum vulgare |
| linkage mapping populations |
can be used to |
produce linkage maps |
|
| different environmental effects across populations (GxE) |
can cause |
effects mapped in a given local population may not be portable to others |
|
| genetic map of Sq-1×Sorbo |
was constructed using |
78 markers and JoinMap4 software |
Arabidopsis thaliana |
| QTLs CsFW1.1, CsTW1.1, and CsDW1.1 |
explained |
9%, 10.2%, and 9.8% of total variance of their traits |
Arabidopsis thaliana |
| SNP or InDel markers |
distinguish |
parental genotypes |
Hordeum vulgare |
| several transcription factors and an auxin-related gene |
require |
further fine mapping |
Hordeum vulgare |
| mapping approaches |
identify |
causal polymorphism |
Arabidopsis thaliana |
| complicating factors |
are reduced but not eliminated in |
local populations |
|
| differences in epistatic effects (GxG) when genetic backgrounds vary among populations |
can cause |
effects mapped in a given local population may not be portable to others |
|
| (CYP707A3, AT5G45340) |
is located in |
genomic region between At5g-102 and nga129 |
Arabidopsis thaliana |
| genomic DNA |
used as template for |
PCR-based mapping |
Arabidopsis thaliana |
| L4168 marker |
is |
Indel marker type |
Oryza sativa |
| small 158-plant F2 population |
genotyped using |
markers RM5503 and L4160 |
Oryza sativa L. |
| mapping population of backcross inbred lines (BILs) |
is characterized by |
minimal segregation in days to heading (DTH) |
|
| fine mapping of QTL causal genes |
requires |
lengthy and involved process |
Zea mays |
| plasticity index phenotype |
was used to identify |
reliable QTLs involved in heat response |
|
| highest concentration of SNPs significantly associated with Fv'/Fm' |
was found between |
(OTP71, AT1G64310) and (AT1G64320) |
Arabidopsis thaliana |
| dupw167 and stem rust data combined |
showed |
53 AASS, 2 AARS, 80 ABRS and 45 BBRR plants |
Triticum polonicum; Triticum aestivum |
| quantitative trait loci (QTL) mapping |
has been widely applied in |
plant genomics |
|
| map-based cloning of causal mutations |
links |
specific mutations to traits of interest |
|
| genome wide association mapping |
is expected to work well for |
traits controlled by hard sweeps |
|
| GWAS within more than one local population |
could avoid |
insufficient genetic variation pitfall |
|
| slower LD decay in two-way RILs |
may reduce |
mapping definition of the panel |
Zea mays |
| QTL mapping |
mapped |
QTLs for 11 traits |
|
| 10 genes |
common to |
three environments |
Medicago truncatula |
| homozygous recombinants |
delimited Spr3 locus to region between |
markers L4355 and L4264 |
Oryza sativa |
| L4264 marker |
is |
CAPS marker type |
Oryza sativa |
| (AtKAT1, KAT1, AT5G46240) |
is located in |
genomic region between At5g-102 and nga129 |
Arabidopsis thaliana |
| 200 BC3 F2 plants |
was used to produce |
high-resolution linkage map of Spr3 region |
Oryza sativa |
| heterozygous plants from BC3F2 population |
used to construct |
F2 population |
Oryza sativa L. |
| homozygous for CG-14 chromosomal segment plants |
selected as |
controls |
Oryza sativa L. |
| seven markers |
mapping in upper arm of chromosome 1 showed distortion from expected 1:1 segregation of homozygous genotypes |
homozygous genotypes |
Arabidopsis thaliana |
| inability to form a linkage map |
was caused by |
chromosomal abnormalities |
Atriplex rosea; Atriplex prostrata |
| 21 BC 4 F 2 recombinants |
narrowed down the location of |
qLA4-1 QTL |
|
| nine MTAs for LER |
included one located on |
chromosome (Chr) 2 |
Zea mays |
| Rpi-chc1.2 and Rpi-chc1.1 |
show perfect repulsion |
in recombinant population 6750 |
Solanum chacoense |
| any line carrying Sr13 |
should be positive for |
98 bp band amplified by rwgsnp37.2 |
Triticum aestivum; Triticum turgidum |
| eight tetraploid lines |
carried |
Sr13 |
Triticum turgidum |
| growth models |
highlight importance of applying |
to QTL analysis |
Hordeum vulgare |
| Ppd-H1 specific marker |
confirmed |
Ppd-H1 segregating within Mundah × Keel RIL population |
Hordeum vulgare |
| bi-parental (recombinant inbred lines, RILs; introgression lines, ILs; F 2 ) populations |
is example of |
specialized genetic resources/genetic stocks |
|
| Synthetic mapping populations |
can eliminate |
rare variants and geographic population structure |
|
| Spr3 locus |
was mapped on region between |
markers L4213 and L4218 |
Oryza sativa |
| L4316 marker |
is |
CAPS marker type |
Oryza sativa |
| exploring the range of genetic variation for herbivore-induced plant volatiles (HIPV) |
is |
prerequisite |
|
| halophytic plants |
lack |
genetic tools including molecular markers for positional cloning |
|
| Association mapping (AM) |
is adopted as method complementary to |
traditional bi-parental linkage mapping |
|
| inter-mutant crosses among approximately 100 suppressor mutants |
placed mutants in |
complementation groups |
Arabidopsis thaliana |
| BrSIO3 |
accounted for |
14.5% of the variance |
Brassica rapa |
| matrixin proteins ( (AT2G45040) in BrSIO1 and (AT1-MMP, AT4G16640) in BrSIO2) |
are |
candidate responsible genes |
Arabidopsis thaliana |
| RADseq |
is |
a powerful method for genetic marker discovery and genetic map construction for pear |
|
| Most studies linking genetic markers and parameters of an ecophysiological model |
were carried out after |
measuring parameters on a mapping population |
|
| (ATCAL4, CML12, TCH3, AT2G41100) |
is located within |
2 Mb region of nga168 |
Arabidopsis thaliana |
| recombinants between markers and Spr3 locus |
number indicated under |
high-resolution linkage map |
Oryza sativa |
| putative GID1 GA receptor sequence in barley |
corresponds to |
Gse1 locus |
Hordeum vulgare |
| L4259 marker |
is |
Indel marker type |
Oryza sativa |
| Md-PG1 SNP functional marker |
was applied to |
Fuji (Fj) × Mondial Gala (MG) population |
|
| GM 862 crossed with wild-type Landsberg erecta (Ler) |
generated |
F1 plants heterozygous for polymorphic markers between Col and Ler |
Arabidopsis thaliana |
| complementation tests with syp121–1 syp122–1 ssd mutants with similar phenotype |
led to identification of |
15 new (ATICS1, EDS16, ICS1, SID2, AT1G74710) mutants |
Arabidopsis thaliana |
| fine-mappings |
were performed using |
Cereon Col/L er marker information |
Arabidopsis thaliana |
| L4327 marker |
is |
Indel marker type |
Oryza sativa |
| newly available marker technologies |
allow |
characterization and positioning of loci that control herbivore-induced plant volatiles (HIPV) traits |
|
| only one pQTL common to the two populations |
denotes |
the polygenic nature of tomato heat response |
|
| high-quality and high-density single-nucleotide polymorphism (SNP) markers |
enable |
high-resolution mapping by genome-wide association studies (GWASs) |
|
| QTL on the short arm of chromosome 2H at 34.25 cM for PSA.smooth |
was detected for |
PSA.smooth at 24 and 28 DAP |
Hordeum vulgare |
| expression of cytochrome P450 superfamily protein |
only detectable in |
grains |
Hordeum vulgare |
| classical linkage analysis |
provides resolution to determine |
genetic variants shaping phenotypic diversity |
|
| QTLs CsFW1.2, CsDW1.2, (CsTW), and SrFW1.2 as well as SrDW1.2 |
showed |
same peak maxima |
Arabidopsis thaliana |
| S-b gene |
has been fine mapped |
S-b gene locus |
Oryza sativa |
| locus controlling number of spikelets per spike |
is mapped to |
distal 83% region of chromosome 1AL arm |
|
| 7.6-kb DNA sequences |
contains |
4.6-kb region |
Oryza sativa |
| minimal variations in rates of photosynthesis among parental varieties |
might be a consequence of |
limited information about QTLs for leaf photosynthesis |
Oryza sativa |
| Populations developed for genetic analysis |
focused on |
regions of chromosome 4 and 8 |
Oryza sativa |
| QTL close to the border of significance |
can appear in |
one population but might not appear in another |
Arabidopsis thaliana |
| S-c gene |
has been fine mapped |
S-c gene locus |
Oryza sativa |
| 105 COSII markers |
are common to |
at least four of the six mapping populations |
Solanum spp.; Solanum tuberosum |
| homeoalleles from different chromosomes |
might be |
detected by rwgsnp7 |
Triticum aestivum |
| several transcription factors and an auxin-related gene |
were found underlying |
genetic region |
Hordeum vulgare |
| many ethnicities |
have been vastly underrepresented in |
GWAS panels |
|
| locus for salt tolerance after SA |
was mapped to the same locus on chromosome 5 in |
Bur-0, Cal-0, Ll-1, and Zu-0 |
Arabidopsis thaliana |
| association mapping in diverse population |
provides |
higher mapping resolution |
Zea mays |
| majority of VTE core pathway enzyme-encoding genes |
are grouped within |
chromosomes 7, 8, and 9 |
Solanum lycopersicum |
| GWA study |
was conducted between |
SNPs and trait values |
Zea mays |
| associations on chromosome 1 |
were not identified using |
environment-independent MTMM model |
Arabidopsis thaliana |
| identified locus on chromosome 1 |
might play a role in regulating |
Fv'/Fm' under salt stress and influenced the interaction between genotype and environment |
Arabidopsis thaliana |
| F1 hybrid from Rusty × PI 387696 cross |
were developed from |
Rusty × PI 387696 cross |
Triticum aestivum; Triticum carthlicum |
| both marker loci barc104 and dupw167 |
are tightly linked to |
Sr13 |
Triticum polonicum; Triticum aestivum |
| dupw167 locus |
had 240 bp amplicon from Rusty assigned as |
allele A |
Triticum polonicum; Triticum aestivum |
| R4 haplotype |
differed from R1 by only |
2 bp at positions G1963C/G655R and G2272C/V758L |
Triticum turgidum |
| Camadi and CAT-A1 |
were assigned to |
haplotype R4 |
Triticum turgidum |
| several of the QTL for PSA.smooth.AGR and PSA.smooth.RGR |
had higher LOD scores than |
PSA.smooth QTL |
Hordeum vulgare |
| chromosomal region |
with no obvious |
candidate gene |
Hordeum vulgare |
| genetic bases of natural variation |
analyzed using |
classical linkage mapping |
Arabidopsis thaliana |
| Ms10 35 locus |
is positioned within |
~80kb region flanked by markers 762K and 843K |
Solanum lycopersicum |
| genes mapped to rice chromosomes |
could provide useful information for |
further studies on fine genetic mapping and cloning the full-length genes of rice that regulate the heat tolerance trait |
Oryza sativa |
| Chromosomes 1H and 2H |
mapped in |
two linkage groups each |
Hordeum vulgare |
| SNP distribution |
is shown in |
Fig. 2 |
|
| pear map generated in this study |
has |
35 common SSR markers with Fiesta map |
|
| L4265 marker |
is |
CAPS marker type |
Oryza sativa |
| 137 recombinants |
narrowed down |
Spr3 locus |
|
| eight markers |
were developed in |
target region flanked by L4359 and L4293 |
|
| F2 populations |
were generated for |
SSD genes |
Arabidopsis thaliana |
| Md-PG1 SNP functional marker |
segregated in |
Fuji (Fj) × Mondial Gala (MG) population |
|
| QTL analysis |
is useful for identifying |
genes involved in Cs+ and Sr2+ accumulation variation |
Arabidopsis thaliana |
| chromosome segment substitution lines (CSSLs) |
have been developed for |
genetic analysis |
Oryza sativa |
| precise locations of regions |
were determined |
|
Oryza sativa |
| inadequate understanding of factors contributing to differences in photosynthetic rate |
might be a consequence of |
limited information about QTLs for leaf photosynthesis |
Oryza sativa |
| potato diploid population F1840 |
is one of |
six mapping populations being anchored to COSII markers |
Solanum tuberosum |
| AtSAUR46 |
is located within |
2 Mb region of nga168 |
Arabidopsis thaliana |
| introgression mapping |
allowed |
drawing of a tentative structural-functional map of the 7AL-7AgL region |
Triticum turgidum |
| QTL 12 |
has PVE of |
14% |
|
| SSR marker map location |
was compared with |
previous pear and apple maps |
|
| CH02c02b, CH01d03, and CTG1064355 |
are located at |
55.3 cM, 19.6 cM, and 55.3 cM on LG4 in Barlett map |
|
| many SSR markers |
have been shown to have good transferability between |
apple and pear |
|
| quantitative trait loci (QTL) analysis |
was performed on |
recombinant inbred lines (RILs) |
Arabidopsis thaliana |
| extension 'kws' |
indicates that |
the probe was mapped in mapping populations different from Beetmap |
Beta vulgaris |
| segregation distortion |
does not significantly alter |
the map |
Solanum lycopersicum |
| three cultivars with different responses to cyclic water stress |
were selected in order to |
identify genomic regions controlling drought tolerance in wheat |
|
| genes underlying allelic variation |
needs to be |
expanded for breeding programs |
|
| ERECTA locus |
has been identified as |
major QTL for various traits including mineral concentrations |
Arabidopsis thaliana |
| Clipper and Sahara |
are |
parents of a mapping population |
Hordeum vulgare |
| marker pairs with inter-marker distance within 10 cM |
had average D' value of |
0.54±0.24 |
Triticum turgidum subsp. durum |
| genetic map produced from the 192 F2 progeny |
shows |
a 4.3 cM interval between markers 003G03 and 003A03 |
Medicago truncatula |
| F3 segregating population from F2 recombinants |
was used for |
fine mapping |
Hordeum vulgare |
| this study |
presents |
integration of genetic and physical maps |
Beta vulgaris |
| QTL analysis |
requires |
development and selection of DNA markers for linkage analysis |
|
| (HPD, HPPD, PDS1, AT1G06570) (2) |
mapping to |
chromosome 5 |
Solanum lycopersicum |
| four genes mapped on chromosome 9: (APG1, E37, IEP37, VTE3, AT3G63410) (1), (VTE5, AT5G04490) arogenate dehydrogenase [tyra(2)], and geranylgeranyl pyrophosphate synthase [ggps(4)] |
co-localize with |
QTL for α-tocopherol content |
Solanum lycopersicum |
| integrated map |
was generally consistent with |
Tomato-EXPEN 2000 map |
Solanum lycopersicum |
| a QTL for earliness per se in the distal region of chromosome 1A m L |
was designated |
Eps-A m 1 |
Triticum monococcum L. |
| AroDH-4 gene |
is located on |
chromosome 9 |
Zea mays |
| regions of chromosome 4 and 8 |
were large among |
CSSLs from Sasanishiki and Habataki |
Oryza sativa |
| marker RG213 |
is located at |
chromosome 6, position ∼33.5 cM |
|
| SSR marker 34TC15 |
was found to co-segregate with |
AIN phenotype for the 192 F2 plants |
Medicago truncatula |
| genetic map |
includes |
90 markers evenly distributed at average distance of 4.9 cM |
Arabidopsis thaliana |
| DNA markers |
have been developed in |
rice |
Oryza sativa |
| a4 gene |
mapped within |
segment bounded by markers G227 and R712 |
Oryza sativa |
| genotypic variation |
was dissected into distinct loci by |
QTL mapping |
Oryza sativa |
| three complementation groups |
consist of |
ten, seven and seven alleles respectively |
Arabidopsis thaliana |
| presence of Md-PG1 SNP marker band |
occurred in individuals sharing |
heterozygous Md-PG1 allelotype of Mondial Gala (MG) (G/T) |
|
| integrated map |
is 21% shorter than |
Tomato-EXPEN 2000 map |
Solanum lycopersicum |
| F2 data |
were re-analysed to position |
AIN locus between SSR markers 003G03 and 003A03 on chromosome 3 |
Medicago truncatula |
| SSR marker locus Xpsr3094 |
resides in |
the chromosomal region delimited by the 7AL-7AgL BPs of R112-4 and R23-1 recombinants |
Triticum turgidum |
| 17 genes involved in the response of rice to high temperature stress at the milky stage |
were mapped to |
different linkage groups on the rice chromosomes |
Oryza sativa |
| loci underlying length of FLA–BOOT interval |
are QTL 2 on chromosome arm 1BL, QTL 3 on chromosome arm 2BS, and QTL 8 on chromosome arm 5AS |
QTLs controlling FLA–BOOT interval |
|
| two QTL for leaf senescence |
were mapped |
in the Bur-0 × Col-0 population |
Arabidopsis thaliana |
| metaQTL5.2 |
is |
an incongruent locus clustering only two initial QTL |
Arabidopsis thaliana |
| 127 markers |
polymorphic between parents of |
DECO population |
Hordeum vulgare |
| time and labour required |
makes most of them unsuitable for |
fine mapping of traits of interest |
Pyrus spp. |
| low marker density in LG1 |
indicates |
lower rate of heterozygosity in (ATDDM1, CHA1, CHR01, CHR1, DDM1, SOM1, SOM4, AT5G66750) |
|
| total number of markers |
may have increased without |
proportional increase in information |
Triticum aestivum |
| QTL for seed IP6, Mn, and K concentrations |
did co-locate |
in Ler/Kond RILs |
Arabidopsis thaliana |
| physical mapping data for this region of the genome |
allowed |
design of a new SSR marker within this interval |
Medicago truncatula |
| three markers tightly linked to the three known loci mediating interactions with aphids |
include |
34TC15 at AIN; 004H01 at (123B, AKR, AKRP, EMB16, EMB2036, STT2, AT5G66055) h2_1e24a at TTR |
Medicago truncatula |
| SSR markers |
are distributed across |
maize chromosomes |
Zea mays |
| 17 of the 25 genes |
co-segregated with 16 markers in the RILs and were mapped to |
different linkage groups on rice chromosomes 1, 2, 3, 4, 5, 6, 7, 9, and 10 |
Oryza sativa |
| QTL 11 in LDV-grown plants |
has LOD below threshold of 3 with |
LOD of 2.9 and PVE of 14% |
|
| BrSIO3 |
is located near |
BrSIO2 |
Brassica rapa |
| LG1 |
has |
fewest markers and lowest density |
|
| integrated pear linkage map |
consists of |
3,143 SNPs and 98 SSR markers |
|
| each of 17 linkage groups of pear maps |
has |
at least one common marker |
|
| recombination breakpoint in recombinant R378 |
occurred between |
1175 bp and 1695 bp upstream of the (B80, PUB8, AT4G21350) initiating codon |
Arabidopsis thaliana |
| recombination |
was substantially lower in |
all five pericentromeric regions |
Arabidopsis thaliana |
| Mu insertion |
showed perfect co-segregation with |
opaque phenotype |
Zea mays |
| variation between RILs |
allowed |
mapping of QTL for the ten studied traits in each population |
Arabidopsis thaliana |
| Shoot Growth 1 (ASI1, IBM2, SG1, AT5G11470) locus |
was consistently detected |
on chromosome 5, for several yield-related traits in the Bur-0 × Col-0 and Ct-1 × Col-0 populations |
Arabidopsis thaliana |
| F2 population |
was used for |
genetic analyses of CO2 sensitivity |
Brassica rapa |
| BrSIO2 |
is located on |
A03 |
Brassica rapa |
| SULF gene |
was mapped to |
centromeric heterochromatin of tomato chromosome 2 |
Solanum lycopersicum |
| centromeric heterochromatin of tomato chromosome 2 |
lacks |
any other genetic marker in close proximity |
Solanum lycopersicum |
| recombination rate |
is homogeneously distributed along five chromosomes with average value of |
391 kb cM −1 |
Arabidopsis thaliana |
| LOD values associated with these loci |
range from |
4.5 to 12.3 |
|
| metaQTL5.3 |
clusters |
QTL detected in the Ct-1 × Col-0 and Cvi-0 × Col-0 populations |
Arabidopsis thaliana |
| LG1, LG4, and LG7 |
have |
fewer markers and peaks |
|
| LG7 and LG13 |
have no common markers in |
apple Fiesta map |
|
| DES and target loci |
mapped to |
known rice QTL related to nine categories of agronomic traits |
Oryza sativa |
| QTL on IL 9-1 |
spans the genomic region containing |
tyra(2) and ggps(4) |
Solanum lycopersicum |
| tomato |
was one of the first crops to have |
saturated genetic linkage map |
Solanum lycopersicum |
| Solanum chmielewskii IL population |
is being anchored to |
common set of COSII markers |
Solanum chmielewskii |
| published genetic markers |
were used to analyze |
22 rescued F2 plants |
Arabidopsis thaliana |
| L4324 marker |
is |
Indel marker type |
Oryza sativa |
| recombinant event |
occurred between |
markers L4355 and L4324 |
|
| molecular markers RM5503 and L4160 |
used for |
preliminary mapping |
|
| test statistics and thresholds for QTL evidence |
were calculated by |
MapQTL5 software |
Arabidopsis thaliana |
| four significant recombination QTLs (rQTLs) in a joint additive model |
explained |
64.4% of the variation in crossover frequency |
Arabidopsis thaliana |
| nine linkage groups |
assigned to |
chromosome numbers in accordance with the information of Schondelmaier and Jung (1997) |
Beta vulgaris |
| EST-derived markers |
represent |
gene densities |
Beta vulgaris |
| AE4 gene |
was mapped to |
lower arm of chromosome 2 |
Arabidopsis thaliana |
| a few of Eps genes |
have been mapped as |
quantitative trait loci (QTL) for heading time |
|
| three mineral QTL hotspots |
were also |
hotspots for QTLs of life history traits in Ler/Cvi population |
Arabidopsis thaliana |
| marker pairs with inter-marker distance within 10-20 cM |
showed significant LD in |
61% |
Triticum turgidum subsp. durum |
| anthranilate phosphoribosyltransferase (APT, EC 2.4.2.18) |
identified at |
59 cM of chromosome 6 |
Solanum lycopersicum |
| QTL for Rubisco content in rice |
overlaps with |
QTL OzT8 |
Oryza sativa |
| Solanum neorickii LA2133 backcross inbred lines (BIL) |
is one of |
six mapping populations being anchored to COSII markers |
Solanum neorickii |
| high-throughput markers |
remain a limited resource |
many markers selected based on polymorphisms in wide crosses are not polymorphic within cultivated germplasm |
Solanum lycopersicum |
| mapping population derived from cross between Ler and Eringsboda |
is |
new mapping population included in this study |
Arabidopsis thaliana |
| deletion in (AGL25, FLC, FLF, RSB6, AT5G10140) |
was not detected in |
GWAS |
Arabidopsis thaliana |
| BSA-seq and transcriptome analysis |
were used on |
F1 progeny from 'Changfu 2' × 'Golden Delicious' cross |
|
| better marker coverage of these regions |
is |
a further objective |
Triticum turgidum |
| strong effect of the (ASI1, IBM2, SG1, AT5G11470) locus |
hampered |
detection of other minor QTL, especially in the Bur-0 × Col-0 population |
Arabidopsis thaliana |
| BrSIO1 and BrSIO2 |
do not have |
the same genetic origin |
Brassica rapa |
| genetic control of midday leaf water potential under stabilized evaporative and soil water deficit conditions |
confirmed by detection of |
several underlying QTLs on consensus map |
grapevine |