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Bioinformatics Unit 1: Data Bases and Alignments
Bioinformatics Unit 1: Data Bases and Alignments

... • Sequence alignments allow comparison of new sequences to either one, a group of, or all known sequences • A well-designed alignment can allow one to infer: – gene or protein function – evolutionary relationships among genes, proteins or species – structure of proteins of nucleic acids ...
6.5 Genetic engineering - science
6.5 Genetic engineering - science

... Changing the genetic code Bacteria are often genetically engineered to produce useful chemicals because their DNA is loose in the cytoplasm, making it easy to modify. They also grow and replicate quickly. ...
Gregor Mendel Versuche über Pflanzenhybriden
Gregor Mendel Versuche über Pflanzenhybriden

... In retrospect, we see that the overwhelming majority of traits in humans, other animals, and plants – traits that are of most interest and importance from a public health, and other societally relevant perspectives (height, weight, body plan, facial appearance, skin color) – are quantitative. Mendel ...
A comparative genomic study among various gene families related
A comparative genomic study among various gene families related

... Basidiomycete species are a key component in wood degradation and have a great influence in carbon cycling. Two major mechanisms of wood decay have been characterized, termed white rot and brown rot. White rot species effectively degrade lignin, cellulose and hemicellulose while brown rot species de ...
SUMMARY OF PROFESSIONAL ACCOMPLISHMENTS
SUMMARY OF PROFESSIONAL ACCOMPLISHMENTS

... the Thermus sp. enzyme family are not highly expressed in E. coli. Moreover, these genes are relatively difficult to clone because they encode enzymes with ENase activity, potentially "toxic" for bacterial host cell. The accompanying MTase activity is not sufficient to protect the DNA of the genomic ...
Solution
Solution

... 17. A. (4 points) In dogs, achondroplasia (short limb bones) results from a haplotype  containing a retrotransposed copy of the Fibroblast Growth Factor 4 (FGF4) gene.  In the  genome of dog breeds with achondroplasia, a second copy of the FGF4 gene is found, and  appears to have resulted from retro ...
Ribosomal DNA sequences reveal gregarine pathogens
Ribosomal DNA sequences reveal gregarine pathogens

Aipotu Part III: Molecular Biology
Aipotu Part III: Molecular Biology

... • This report is due in class today; you can write it using Microsoft Word on the lab macs and then print it on the lab printer. • This is a group project for a group grade. • Although you worked together as a class, your report must be in your own words. Your lab report must consist of answers to t ...
How Do Heritable Changes in Genes Occur?
How Do Heritable Changes in Genes Occur?

... Because UV irradiation is about the easiest and surest way of inducing DNA damage experimentally, UV is one of the most extensively studied mutagens. It can damage the DNA in several ways, but the most common is by causing the formation of a pair of covalent bonds between adjacent thymine residues i ...
Clinical detection and characterization of bacterial pathogens in the genomics era
Clinical detection and characterization of bacterial pathogens in the genomics era

... and nosocomial or pandemic infections, a higher discriminatory power is needed to be able to trace pathogens at the strain level. Identifying bacteria at the strain level - or bacterial strain typing - is particularly important for epidemiological surveillance of infections. Strain typing also has a ...
1d Mapping lab
1d Mapping lab

... The BAM files show the reads aligned to the reference genome, but they do not directly tell you which genes or transcripts are actually expressed. A tool that does that is Cufflinks (http://cole-trapnell-lab.github.io/cufflinks/). If a gene has several isoforms, Cufflinks predicts the expression ...
Chapter 8: From DNA to Proteins
Chapter 8: From DNA to Proteins

...  A mutation can break up a gene, or it can make a new hybrid gene, with a new function.  Gene mutations can cause the wrong amino acid to be made which can change an entire protein. Impact on Offspring  Mutations in sex cells can be passed on to offspring.  They are the underlying source of gene ...
Overview of Recombinant DNA Experiments Covered by
Overview of Recombinant DNA Experiments Covered by

... into the embryo, you must register this work. Knock-out Animals Knock-out (gene silencing, gene ablation, etc.) rodents are exempt from the NIH Guidelines as long as the method to generate the knock-out animal does not leave any “new” genetic material behind in the genome after the procedure. If DNA ...
Chapter 20~ DNA Technology & Genomics
Chapter 20~ DNA Technology & Genomics

Multiple Barriers to Nonhomologous DNA End Joining
Multiple Barriers to Nonhomologous DNA End Joining

... semipermeable barrier) between the sister chromatids that promotes homolog exchange, possibly involving the activity of chromosome axis proteins (Couteau et al. 2004; Webber et al. 2004; Niu et al. 2005; Kim et al. 2010; Li et al. 2011). Finally, homologous repair must be promoted while more error-p ...
Opportunities of New Plant Breeding Techniques
Opportunities of New Plant Breeding Techniques

... Sequence-specific nucleases (SSN) are synthetic proteins that are designed in the lab. These proteins bind to a specific DNA target sequence and induce a lesion at that position in the DNA. With this technology genes at any location in the DNA can be stably knocked-out, mutated, or replaced. The DNA ...
Nucleic Acids and Chromatin
Nucleic Acids and Chromatin

... A. Chemical structure and nomenclature of the nucleotides. 1. DNA and RNA are polymers of nucleotides (polynucleotides). Nucleotides contain a base, a sugar and a phosphate. a. The base is either a purine (A & G), or a pyrimidine (T & C for DNA or U & C for RNA). In many cases the bases contain chem ...
Supplementary Methods.
Supplementary Methods.

... Potential scoring bias. Because our motif conservation score is based on the number of conserved motifs, the top predictions tended to be more conserved and longer than the average. Since we had found that longer, more conserved fragments are more likely to function as enhancers in our assay, we con ...
Chapter Eleven: Chromosome Structure and Transposable Elements
Chapter Eleven: Chromosome Structure and Transposable Elements

... Furthermore, retrotransposons transpose through an RNA intermediate and depend on reverse transcriptase for transposition, whereas composite transposons transpose through DNA intermediates by the action of transposases encoded by one of their insertion sequences. 17. Explain how Ac and Ds elements p ...
DNA
DNA

Title: Genetics: Mitochondrial DNA in evolution and disease Douglas
Title: Genetics: Mitochondrial DNA in evolution and disease Douglas

1 Today: Genetic and Physical Mapping Sept 2. Structure and
1 Today: Genetic and Physical Mapping Sept 2. Structure and

... Long-range restriction maps: locate the positions of rare-cutting endonuclease recognition sites on a DNA molecule by PFGE Clone (contig) maps: consist of libraries of overlapping clones where the relationship of each clone to other clones has been resolved Fluorescent in situ hybridization (FISH): ...
Genetic Control of Cell Function and Inheritance
Genetic Control of Cell Function and Inheritance

... Proteins are made from a standard set of amino acids, which are joined end to end to form the long polypeptide chains of protein molecules. Each polypeptide chain may have as many as 100 to more than 300 amino acids in it. The process of protein synthesis is called translation because the genetic co ...
Booklet 3
Booklet 3

... (b) In situations where symptoms of Huntington’s appear in one or both partners and there are children, the family is usually referred to a genetic counsellor. One of the options which will be discussed is whether any existing children of the couple should be tested for the presence of the Huntingt ...
Germ Line Transmission and Expression of a Corrected HPRT Gene
Germ Line Transmission and Expression of a Corrected HPRT Gene

... Caskey, 1988). Consequently, it is noteworthy that, in normal individuals, HPRT expression is elevated in brain relative to other tissues. Hooper et al. (1987) selected for spontaneous HPRT-deficient ES cells in culture. Kuehn et al. (1987) used multiple retroviral infection of cultured ES cells to ...
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Genome editing

Genome editing, or genome editing with engineered nucleases (GEEN) is a type of genetic engineering in which DNA is inserted, replaced, or removed from a genome using artificially engineered nucleases, or ""molecular scissors."" The nucleases create specific double-stranded break (DSBs) at desired locations in the genome, and harness the cell’s endogenous mechanisms to repair the induced break by natural processes of homologous recombination (HR) and nonhomologous end-joining (NHEJ). There are currently four families of engineered nucleases being used: Zinc finger nucleases (ZFNs), Transcription Activator-Like Effector Nucleases (TALENs), the CRISPR/Cas system, and engineered meganuclease re-engineered homing endonucleases.It is commonly practiced in genetic analysis that in order to understand the function of a gene or a protein function one interferes with it in a sequence-specific way and monitors its effects on the organism. However, in some organisms it is difficult or impossible to perform site-specific mutagenesis, and therefore more indirect methods have to be used, such as silencing the gene of interest by short RNA interference (siRNA) . Yet gene disruption by siRNA can be variable and incomplete. Genome editing with nucleases such as ZFN is different from siRNA in that the engineered nuclease is able to modify DNA-binding specificity and therefore can in principle cut any targeted position in the genome, and introduce modification of the endogenous sequences for genes that are impossible to specifically target by conventional RNAi. Furthermore, the specificity of ZFNs and TALENs are enhanced as two ZFNs are required in the recognition of their portion of the target and subsequently direct to the neighboring sequences.It was chosen by Nature Methods as the 2011 Method of the Year.
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