Pages that link to "Q73275495"
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The following pages link to Bias in multipoint linkage analysis arising from map misspecification (Q73275495):
Displaying 49 items.
- Localization of a susceptibility gene for common forms of stroke to 5q12 (Q24632864) (← links)
- Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4). (Q24648625) (← links)
- Whole-genome scan, in a complex disease, using 11,245 single-nucleotide polymorphisms: comparison with microsatellites (Q28262660) (← links)
- A high-resolution recombination map of the human genome (Q29547815) (← links)
- Identification of novel susceptibility loci for Guam neurodegenerative disease: challenges of genome scans in genetic isolates (Q30490128) (← links)
- Look before you leap: a new approach to mapping QTL. (Q30866902) (← links)
- The impact of data quality on the identification of complex disease genes: experience from the Family Blood Pressure Program (Q31032793) (← links)
- Linkage analysis of alcohol dependence using MOD scores (Q33232756) (← links)
- Comparison of microsatellites, single-nucleotide polymorphisms (SNPs) and composite markers derived from SNPs in linkage analysis (Q33232771) (← links)
- A high-resolution single nucleotide polymorphism genetic map of the mouse genome (Q33263584) (← links)
- A genome-wide Asian genetic map and ethnic comparison: the GENDISCAN study (Q33386269) (← links)
- Regional differences in recombination hotspots between two chicken populations (Q33530230) (← links)
- Enhanced genetic maps from family-based disease studies: population-specific comparisons (Q33797390) (← links)
- Exploration of the disease locus by a careful evaluation of the likelihood polynomial for pedigree data (Q33848886) (← links)
- A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set. (Q33905163) (← links)
- Evidence for extensive transmission distortion in the human genome (Q33909560) (← links)
- Evidence for a novel late-onset Alzheimer disease locus on chromosome 19p13.2. (Q33910032) (← links)
- Transmission-ratio distortion and allele sharing in affected sib pairs: a new linkage statistic with reduced bias, with application to chromosome 6q25.3. (Q33910138) (← links)
- Guidelines for genotyping in genomewide linkage studies: single-nucleotide-polymorphism maps versus microsatellite maps (Q33910203) (← links)
- Linkage analysis in the presence of errors II: marker-locus genotyping errors modeled with hypercomplex recombination fractions (Q34145292) (← links)
- Linkage analysis in the presence of errors III: marker loci and their map as nuisance parameters (Q34145558) (← links)
- Characterizing uncertainty in high-density maps from multiparental populations. (Q34242860) (← links)
- Large-scale integration of human genetic and physical maps (Q34343089) (← links)
- A high density recombination map of the pig reveals a correlation between sex-specific recombination and GC content. (Q34478154) (← links)
- A novel Markov chain monte carlo approach for constructing accurate meiotic maps (Q34589716) (← links)
- A linkage search for joint panic disorder/bipolar genes (Q34683418) (← links)
- A male-specific quantitative trait locus on 1p21 controlling human stature (Q35447506) (← links)
- Sex-specific genetic architecture of human fatness in Chinese: the SAPPHIRe Study. (Q35655481) (← links)
- Linkage analysis of adult height with parent-of-origin effects in the Framingham Heart Study (Q35786651) (← links)
- Joint oligogenic segregation and linkage analysis using bayesian Markov chain Monte Carlo methods (Q38638740) (← links)
- Construction of a High-Density Genetic Map and Quantitative Trait Locus Mapping in the Sea Cucumber Apostichopus japonicus (Q36124296) (← links)
- A second-generation combined linkage physical map of the human genome (Q36177402) (← links)
- An evolutionary view of human recombination (Q36673942) (← links)
- Genomewide scan for real-word reading subphenotypes of dyslexia: novel chromosome 13 locus and genetic complexity (Q36916885) (← links)
- The human pseudoautosomal regions: a review for genetic epidemiologists (Q37132730) (← links)
- A high-density SNP-based linkage map of the chicken genome reveals sequence features correlated with recombination rate (Q37142016) (← links)
- Detection and integration of genotyping errors in statistical genetics (Q37360857) (← links)
- Localization of a gene for peripheral arterial occlusive disease to chromosome 1p31. (Q37361172) (← links)
- Annotated chromosome maps for renal disease (Q40018059) (← links)
- Summary of Genetic Analysis Workshop 15: Group 9 linkage analysis of the CEPH expression data (Q42638258) (← links)
- Distribution and magnitude of type I error of model-based multipoint lod scores: implications for multipoint mod scores (Q44024681) (← links)
- Evidence for multiple loci from a genome scan of autism kindreds. (Q50303249) (← links)
- Using sex-averaged genetic maps in multipoint linkage analysis when identity-by-descent status is incompletely known. (Q51806050) (← links)
- Empirical significance values for linkage analysis: trait simulation using posterior model distributions from MCMC oligogenic segregation analysis. (Q51906177) (← links)
- Genetic maps of microsatellite and single-nucleotide polymorphism markers: are the distances accurate? (Q52950187) (← links)
- Characteristics of genetic markers and maps for cost-effective genome screens using diallelic markers (Q58047715) (← links)
- Genome-wide scan in a large complex pedigree with predominantly male schizophrenics from the island of Kosrae: evidence for linkage to chromosome 2q (Q73696937) (← links)
- The Iceland map (Q74254706) (← links)
- Improving estimates of genetic maps: a meta-analysis-based approach (Q80179930) (← links)