Basic Human Genetics 2009
| Submitted: | Wednesday 29th of September 2010 04:48:34 PM |
|---|---|
| Submitted by: | Mohammed-E Twfieg |
| Language: | English |
| Educational levels: | qc1, qc2 |
Topics
- Statistical genetics > Genetic epidemiology > Gene discovery > Genome-wide > Linkage (Genome-wide)
- Clinical/medical genetics > Genetic counselling > Risk assessment > Mendelian pattern
- Statistical genetics > Mathematical models used in statistical genetics > Formal genetics > Mendelian laws
- Molecular genetics > Studies of DNA > Gene expression
- Statistical genetics > Genetic epidemiology > Gene discovery > Candidate > Association (Candidate)
- Molecular genetics > Studies of DNA > Studies of DNA (as a sequence) > Human variability (SNPs/microsatellites/copy-number variation)
- Molecular genetics > Studies of DNA > Studies of DNA (as a sequence) > Disease-associated alterations (mutation/deletion/duplication/insertion)
- Molecular genetics > Techniques > Molecular techniques > PCR
- Statistical genetics > Mathematical models used in statistical genetics > Population genetics > LD
- Molecular genetics > Techniques > Array based/high throughput technologies
- Molecular genetics > Techniques > Molecular techniques > Sequencing
- Clinical/medical genetics > Patient related > Population related > Genomics
- Molecular genetics > Studies of chromatin > Structure of chromosome
- Molecular genetics > Studies of chromatin > Meiosis
- Clinical/medical genetics > Disease related (typology of disorder) > Single gene disorders
- Molecular genetics > Techniques > Molecular techniques > Cloning
- Molecular genetics > Techniques > Cell-biological assays > Cell and tissue culture models
- Molecular genetics > Studies of RNA > Studies of coding RNA > Studies of protein > Protein quantity
- Statistical genetics > Genetic epidemiology > Gene discovery > Candidate > Linkage (Candidate)
Abstract
This Learning Package contains material in Basic Human Genetics, which was given to students in the MSc in Molecular Medicine, at the University of Sheffield in 2009.Resources
Wednesday 29th of September 2010 01:37:49 PM - Mohammed-E Twfieg | Language: English |
Content type: Learning resource
A lecture in human genetics that was delivered as part of MSc in Molecular Medicine at the University of Sheffield in 2009.
Wednesday 29th of September 2010 02:33:10 PM - Mohammed-E Twfieg | Language: English |
Content type: Learning resource
A lecture in human genetics that was delivered as part of MSc in Molecular Medicine at the University of Sheffield in 2009.
Wednesday 29th of September 2010 02:55:05 PM - Mohammed-E Twfieg | Language: English |
Content type: Learning resource
A lecture in human genetics that was delivered as part of MSc in Molecular Medicine at the University of Sheffield in 2009.
Wednesday 29th of September 2010 03:07:35 PM - Mohammed-E Twfieg | Language: English |
Content type: Learning resource
A lecture in human genetics that was delivered as part of MSc in Molecular Medicine at the University of Sheffield in 2009.
Wednesday 29th of September 2010 03:24:18 PM - Mohammed-E Twfieg | Language: English |
Content type: Learning resource
This file contains Linkage analysis puzzles given for students of the MSc in Molecular Medicine at the University of Sheffield in 2009.
Wednesday 29th of September 2010 01:31:56 PM - Mohammed-E Twfieg | Language: English |
Content type: Learning resource
A lecture in human genetics that was delivered as part of MSc in Molecular Medicine at the University of Sheffield in 2009.
Keywords
affected, allele, allelic variation, Analysis of the entire coding region: Sequence analysis, antibody, antigen, antiparallel, Array genomic hybridization, association, autosomal, bacteriophage, band, base, base pair, bioinformatics, biotechnology, buccal swab, carrier, cell, cell line, centimorgan, central dogma, chromosome, clone, coding sequence, codon, Complementary DNA, complementary strand, consanguineous, copy number polymorphism, correlation, cos cell, cystic fibrosis transmembrane conductance regulator, cytoplasm, degeneracy, deletion, deoxyribonucleic acid, diploid, dominant, double helix, duplication, dystrophin, electrophoresis, enhancer, epidermal growth factor, eukaryote, exon, expressed gene, expressed sequence tag, expression, fixed, fluorescent in situ hybridization, founder, frequency, gamete, gametogenesis, gene, gene product, gene regulation, genetic map, genetic mapping, genetic marker, geneticist, genetics, genome, genomic dna, genotype, genotyping, germline, haploid, haploid genome, haplotype, heredity, heterogeneous, heterozygote, heterozygous, homologous, homologous chromosome, homozygous, human genome project, human leucocyte antigen, hybrid, in vitro, indels, information content, informative, inherited, insertion, intron, isolate, kilobase, library, linkage, linkage analysis, linkage disequilibrium, locus, long interspersed nuclear element, marker, maternal, meiosis, messenger rna, microarray, microsatellite, mitochondrion, mode of inheritance, monoclonal, monogenic, mutant, mutation, myeloma, neurone, nucleotide, nucleus, oligonucleotide, open reading frame, pedigree, peptide, phase, phenotype, physical distance, plasmid, polyadenylation, polygenic, polymerase, polymerase chain reaction, polymorphism, population, primer, probability, probe, promoter, protein, protein analysis, pseudogene, reading frame, recessive, recombinant, recombination, recombination fraction, recombinational mapping, repetitive dna, replication, reverse transcriptase, ribonucleic acid, rna splicing, screening, selection, sequence, single nucleotide polymorphism, slippage, specie, specificity, spliceosome, splicing, sporadic, substitution, synthesis, telomere, trait, transcript, transcription, translation, unaffected, uninformative, variation, vector, x-chromosomeTerms of use
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported License. Read more.