Basic Genetics (Human Genetics)

Submitted: Friday 17th of September 2010 07:29:27 PM
Submitted by: Mohammed-E Twfieg
Language: English
Educational levels: qc1, qc2

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Abstract

This Learning Package contains within it 2 learning packages in Basic Genetics/Human Genetics, which were taught as part of the MSc in Genetic Epidemiology at the University of Sheffield in 2008.

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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.
This Learning Package contain lectures in Human Genetics, which were taught as part of the MSc in Genetic Epidemiology, at the University of Sheffield in 2008.

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Keywords

18s ribosomal rna, 28s ribosomal rna, 5s ribosomal rna, abnormal, additive, adenine, adenomatous polyposis coli, adenosine triphosphate, admixture, affected, affected sib-pair, allele, allele frequency, allelic variation, alternative splicing, amino acid, amniotic fluid, Analysis of the entire coding region: Sequence analysis, anaphase, ancestral haplotype, aneuploidy, antibody, anticodon, anticodon loop, antigen, antiparallel, AP-1, association, association studies, assortative mating, ATF, autosomal dominant, autosomal recessive, autosome, autozygosity, bacteriophage, balanced translocation, band, banding, base, base pair, beta, biallelic marker, bias of ascertainment, bioinformatics, biotechnology, BRCA, buccal swab, ca repeat, caat box, candidate gene, capping, carrier, case-control, cell, cell cycle, cell division, cell line, centimorgan, central dogma, centric fusion, centriole, centromere, CF allele, chiasma, chromatid, chromatin, chromosome, chromosome abnormality, chromosome structure, chromosome translocation, cis configuration, clone, coding mutation, coding sequence, codominant, codon, common disease, comparative sequencing, Complementary DNA, complementary strand, complete linkage, complex disease, concordance, congenital, copy number polymorphism, correlation, cos cell, cosmid, culture medium, cystic fibrosis transmembrane conductance regulator, cytogenetics, cytogenics, cytokinesis, cytoplasm, cytoplasmic protein, cytosine, deamination, degeneracy, deletion, deoxyribonucleic acid, depurination, diakinesis, dinucleotide repeat, diploid, diplotene, discordant, disjunction, DNA methylation, dna polymerase, dna probe, dna repair, dna replication, dna sequencing, dna structure, dna variant, domain, dominant, dominant allele, double helix, double recombinant, dystrophin, electrophoresis, enhancer, enzyme, epidermal growth factor, ER, euchromatin, eukaryote, euploid, exon, expansion, expressed sequence tag, expression, false positive result, familial, familial adenomatous polyposis, fixed, flanking marker, fluorescent dye, fluorescent in situ hybridization, founder, frameshift, free polyribosome, frequency, functional SNP, g band, gamete, gametogenesis, gc box, gel electrophoresis, gene, gene expression, gene pool, gene product, gene regulation, genehunter, genetic code, genetic disease, genetic heterogeneity, genetic map, genetic map distance, genetic mapping, genetic marker, genetic screen, genetic screening, genetic variation, geneticist, genetics, genome, genome scan, genomic dna, genomic imprinting, genotype, genotyping, genotyping error, germline, germline genetic variation, guanine, guthrie spot, haploid, haploid genome, haploid number, haplotype, haplotype block, helicase, heredity, heritability, heterochromatin, heteroduplex, heterogeneity, heterogeneous, heterozygote, heterozygous, high throughput, histone acetylation, homologous, homologous chromosome, homologous pair, homologous recombination, homozygous, hotspot, human genetic mapping, human genetic marker, human genome project, human leucocyte antigen, hybrid, hydrophobic signal sequence, ibs, identity by descent, in vitro, inbreeding, incomplete linkage, incomplete penetrance, indels, independent assortment, information content, informative, informativeness, inheritance, inherited, insertion, interference, interphase, interstitial deletion, intron, inversion, isolate, isolated, karyotype, kilobase, leptotene, library, linkage, linkage analysis, linkage disequilibrium, linkage group, linkage mapping, locus, locus control region, lod score, long interspersed nuclear element, loss of heterozygosity, map unit, mapping function, marker, maternal, maximum lod score, megabase, meiosis, meiotic anaphase I, meiotic metaphase I, meiotic prophase I, meiotic telophase I, mendelian inheritance, messenger rna, metabolism, metaphase, microarray, microarray chip, microsatellite, minisatellite, mitochondrion, mitosis, mode of inheritance, molecular genetics, monoclonal, monogenic, monogenic disease, monozygotic twins, multifactorial, multipoint, mutant, mutation, mutation rate, myeloma, nonsense mutation, northern blot, nucleoside, nucleotide, nucleus, null allele, okazaki fragment, oligonucleotide, open reading frame, orthologous, outbred population, ova, p1-derived artificial chromosome, pachytene, parametric linkage analysis, parental, parental genotype, pathogenic mutation, pedigree, penetrance, peptide, peptide bond, peptidyl transferase, pericentric, pericentric chromosome inversion, phase, phenocopy, phenotype, phenotypic variation, phosphodiester bond, physical distance, physical map, plasmid, point mutation, pollen, polyadenylation, polyadenylation signal, polygenic, polygenic trait, polymerase, polymerase chain reaction, polymorphism, polyploid, polyribosomes, population, positional cloning, primary transcript, primer, principle of segregation, probability, probe, processing, promoter, prophase, protein, protein analysis, protein truncation test, proteomics, pseudogene, purine, pyrimidine, quantitative PCR, random assortment, random mating, reading frame, recessive, recessive gene, recombinant, recombination, recombination fraction, recombinational mapping, relative risk, repetitive dna, replication, reverse transcriptase, ribonucleic acid, ribose, ribosomal RNA, ring chromosome, rna editing, rna polymerase, rna processing, rna splicing, screening, secreted protein, segmental duplication, segregation, segregation analysis, selection, semi-conservative, sequence, sequence tagged site, sex chromosome, sib, simple repeat, single nucleotide exchange, single nucleotide polymorphism, single stranded conformational polymorphism, sister chromatids, slippage, small nuclear rna, SNP database, somatic, somatic cell, Southern blot, specie, specificity, spindle, spindle poles, splice site, spliceosome, splicing, sporadic, stop codon, stutter band, substitution, synapsis, syndrome, synonymous SNP, synthesis, tandem repeat, target dna, tata box, telomere, telophase, tetranucleotide repeat, TFIID, thymine, trait, trans-acting, transcript, transcription, transcription factor, transcriptionally inactive, transfer rna, transgenic mouse, transition, translation, translocation, transmembrane protein, transmission disequilibrium test, transversion, tre, trinucleotide repeat, triplet, trisomy, tumor suppressor gene, twin studies, u6 small nuclear rna, unaffected, uninformative, uracil, variance, variant, variation, vector, western blot, whole genome screen, wobble at the third base of the codon, x-chromosome, yeast artificial chromosome

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