Basic Human Genetics

Submitted: Friday 17th of September 2010 07:08:18 PM
Submitted by: Mohammed-E Twfieg
Language: English
Educational levels: qc1, qc2

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Abstract

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.

Resources

A lecture in the human genetics module, which was taught as part of the MSc in genetic epidemiology at the University of Sheffield in 2008.
A lecture in the human genetics module, taught as part of the MSc in genetic epidemiology.
A lecture in human genetics, which was taught as part of the MSc in genetic epidemiology at the University of Sheffield in 2008.
This file contains Genetic Mapping Puzzles, which constituted part of the module (From Genome to Gene Function) in the MSc in Genetic Epidemiology, at the University of Sheffield. This module was delivered in 2008.
A lecture in human genetics, which was taught as part of the MSc in genetic epidemiology at the University of Sheffield in 2008.
A lecture in human genetics, which was taught as part of the MSc in genetic epidemiology at the University of Sheffield in 2008.
A lecture in human genetics, which is taught part of the MSc in genetic epidemiology.
A lecture in human genetics, which is taught as part of the MSc in genetic epidemiology.
A lecture in human genetics, which is taught part of the MSc in genetic epidemiology.

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Keywords

abnormal, additive, adenomatous polyposis coli, affected, affected sib-pair, allele, allele frequency, allelic variation, amino acid, amniotic fluid, Analysis of the entire coding region: Sequence analysis, ancestral haplotype, antibody, antigen, antiparallel, association, autosomal dominant, autosomal recessive, autozygosity, bacteriophage, balanced translocation, band, banding, base, base pair, biallelic marker, bioinformatics, biotechnology, buccal swab, ca repeat, candidate gene, carrier, cell, cell division, cell line, centimorgan, central dogma, centromere, CF allele, chromatin, chromosome, chromosome abnormality, chromosome translocation, clone, coding mutation, coding sequence, codominant, codon, comparative sequencing, Complementary DNA, complementary strand, complete linkage, congenital, copy number polymorphism, correlation, cos cell, cosmid, culture medium, cystic fibrosis transmembrane conductance regulator, cytogenetics, cytogenics, cytoplasm, degeneracy, deletion, deoxyribonucleic acid, dinucleotide repeat, diploid, dna polymerase, dna probe, dna replication, dna sequencing, dominant, double helix, dystrophin, electrophoresis, enhancer, enzyme, epidermal growth factor, eukaryote, euploid, exon, expressed sequence tag, expression, familial, familial adenomatous polyposis, fixed, flanking marker, fluorescent dye, fluorescent in situ hybridization, founder, frequency, functional SNP, g band, gamete, gametogenesis, gel electrophoresis, gene, gene expression, gene product, gene regulation, genehunter, genetic disease, genetic map, genetic map distance, genetic mapping, genetic marker, genetic screen, genetic screening, genetic variation, geneticist, genetics, genome, genome scan, genomic dna, genotype, genotyping, germline, germline genetic variation, guthrie spot, haploid, haploid genome, haplotype, haplotype block, heredity, heterochromatin, heteroduplex, heterogeneous, heterozygote, heterozygous, high throughput, homologous, homologous chromosome, homologous pair, homologous recombination, homozygous, hotspot, human genetic mapping, human genetic marker, human genome project, human leucocyte antigen, hybrid, identity by descent, in vitro, inbreeding, indels, independent assortment, information content, informative, inheritance, inherited, insertion, interphase, intron, inversion, isolate, isolated, karyotype, kilobase, library, linkage, linkage analysis, linkage disequilibrium, linkage group, locus, lod score, long interspersed nuclear element, map unit, mapping function, marker, maternal, maximum lod score, megabase, meiosis, mendelian inheritance, messenger rna, metabolism, metaphase, microarray, microarray chip, microsatellite, minisatellite, mitochondrion, mitosis, mode of inheritance, molecular genetics, monoclonal, monogenic, monogenic disease, multipoint, mutant, mutation, myeloma, nonsense mutation, northern blot, nucleotide, nucleus, null allele, oligonucleotide, open reading frame, orthologous, outbred population, p1-derived artificial chromosome, parametric linkage analysis, parental, pathogenic mutation, pedigree, peptide, pericentric, pericentric chromosome inversion, phase, phenotype, phenotypic variation, physical distance, physical map, plasmid, polyadenylation signal, polygenic trait, polymerase, polymerase chain reaction, polymorphism, population, positional cloning, primer, probability, probe, promoter, protein, protein analysis, protein truncation test, proteomics, pseudogene, quantitative PCR, random assortment, reading frame, recessive, recessive gene, recombinant, recombination, recombination fraction, recombinational mapping, repetitive dna, replication, reverse transcriptase, ribonucleic acid, rna polymerase, rna splicing, screening, segmental duplication, segregation, selection, sequence, sequence tagged site, sib, simple repeat, single nucleotide exchange, single nucleotide polymorphism, single stranded conformational polymorphism, sister chromatids, slippage, SNP database, somatic, Southern blot, specie, specificity, spindle, splice site, spliceosome, splicing, stop codon, stutter band, substitution, synapsis, syndrome, synonymous SNP, synthesis, target dna, telomere, tetranucleotide repeat, trait, transcript, transcription, transgenic mouse, translation, translocation, trinucleotide repeat, trisomy, tumor suppressor gene, unaffected, uninformative, variation, vector, western blot, whole genome screen, x-chromosome, yeast artificial chromosome

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