Basic Genetics

Submitted: Thursday 16th of September 2010 05:32:09 PM
Submitted by: Mohammed-E Twfieg
Language: English
Educational levels: qc1, qc2

Abstract

This Learning Package contains lectures that constituted a Basic Genetics module for the MSc students in Genetic Epidemiology at the University of Sheffield. The module provided a foundation for more advanced modules in the MSc. Module was taught in 2008.

Resources

This is the first lecture in the module (Basic Genetics), which provides a foundation in basic genetics as an introduction to the masters program in Genetic Epidemiology.
This is the second lecture in the module (Basic Genetics), which provides a foundation in basic genetics as an introduction to the masters program in Genetic Epidemiology.
This is the fifth lecture in the module (Basic Genetics), which provides a foundation in basic genetics as an introduction to the masters program in Genetic Epidemiology.

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This is the fourth lecture in the module (Basic Genetics), which provides a foundation in basic genetics as an introduction to the masters program in Genetic Epidemiology.
This file contains questions that provide examples/practice supporting the lectures in the Basic Genetics module, which provided a foundation in basic genetics as an introduction to the masters program in Genetic Epidemiology, at the University of Sheffield. The questions include referencing to Stra ...

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This resource is part of the following learning package:

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Keywords

18s ribosomal rna, 28s ribosomal rna, 5s ribosomal rna, additive, adenine, adenosine triphosphate, admixture, affected, affected sib-pair, allele, allele frequency, alternative splicing, amino acid, Analysis of the entire coding region: Sequence analysis, anaphase, aneuploidy, anticodon, anticodon loop, AP-1, association, association studies, assortative mating, ATF, autosomal recessive, autosome, base, beta, bias of ascertainment, BRCA, caat box, capping, carrier, case-control, cell, cell cycle, cell division, centimorgan, centric fusion, centriole, centromere, chiasma, chromatid, chromatin, chromosome, chromosome abnormality, chromosome structure, cis configuration, clone, coding mutation, codon, common disease, Complementary DNA, complex disease, concordance, copy number polymorphism, cosmid, cystic fibrosis transmembrane conductance regulator, cytokinesis, cytoplasmic protein, cytosine, deamination, deletion, deoxyribonucleic acid, depurination, diakinesis, diplotene, discordant, disjunction, DNA methylation, dna repair, dna replication, dna structure, dna variant, domain, dominant, dominant allele, double helix, double recombinant, enhancer, ER, euchromatin, exon, expansion, expression, false positive result, familial, founder, frameshift, free polyribosome, frequency, gamete, gc box, gene, gene expression, gene pool, genehunter, genetic code, genetic heterogeneity, genetic map distance, genetic mapping, genetic marker, genetics, genome, genomic dna, genomic imprinting, genotype, genotyping, genotyping error, germline, guanine, haploid, haploid number, haplotype, helicase, heredity, heritability, heterochromatin, heterogeneity, heterozygous, histone acetylation, homologous chromosome, homologous pair, homozygous, hotspot, hybrid, hydrophobic signal sequence, ibs, identity by descent, inbreeding, incomplete linkage, incomplete penetrance, independent assortment, informativeness, inheritance, inherited, insertion, interference, interphase, interstitial deletion, inversion, isolate, leptotene, linkage, linkage analysis, linkage disequilibrium, linkage group, linkage mapping, locus, locus control region, lod score, loss of heterozygosity, mapping function, marker, meiosis, meiotic anaphase I, meiotic metaphase I, meiotic prophase I, meiotic telophase I, mendelian inheritance, messenger rna, metaphase, microsatellite, mitosis, mode of inheritance, molecular genetics, monogenic, monogenic disease, monozygotic twins, multifactorial, mutation, mutation rate, nonsense mutation, nucleoside, nucleotide, okazaki fragment, ova, pachytene, parametric linkage analysis, parental, parental genotype, pathogenic mutation, pedigree, penetrance, peptide, peptide bond, peptidyl transferase, phenocopy, phenotype, phosphodiester bond, physical distance, physical map, point mutation, pollen, polyadenylation, polyadenylation signal, polygenic, polymerase, polymorphism, polyploid, polyribosomes, population, positional cloning, primary transcript, principle of segregation, probability, processing, promoter, prophase, protein, purine, pyrimidine, random mating, recessive, recessive gene, recombinant, recombination, recombination fraction, relative risk, replication, ribonucleic acid, ribose, ribosomal RNA, ring chromosome, rna editing, rna processing, secreted protein, segregation, segregation analysis, selection, semi-conservative, sequence, sex chromosome, sib, sister chromatids, small nuclear rna, somatic, somatic cell, specie, spindle, spindle poles, splice site, spliceosome, splicing, sporadic, stop codon, substitution, synapsis, syndrome, tandem repeat, tata box, telomere, telophase, TFIID, thymine, trait, trans-acting, transcript, transcription, transcription factor, transcriptionally inactive, transfer rna, transition, translation, translocation, transmembrane protein, transmission disequilibrium test, transversion, tre, triplet, twin studies, u6 small nuclear rna, unaffected, uracil, variance, variant, wobble at the third base of the codon, yeast artificial chromosome

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