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Whole genome sequencing and assembly of an avian genome, the
Whole genome sequencing and assembly of an avian genome, the

... sequenced fragments and makes use of this information to place the different fragments with respect to each other. This method of genome assembly is known as ‘shotgun’ genome sequencing. In this project we tested the benefits of an alternative method for genome assembly called reduced representation ...
Making Sense of Complicated Microarray Data
Making Sense of Complicated Microarray Data

... treatment or mutations, tissue types etc • Continuous scales: time courses, levels of treatment, etc ...
poster
poster

... Predicting Regulatory Elements from Genome-Wide 3-way Alignments of Human, Mouse, and Rat James Taylor, David King, Diana Kolbe, Laura Elnitski, Pallavi Eswara, Jia Li, Webb Miller, Ross Hardison, and Francesca Chiaromonte Center for Comparative Genomics and Bioinformatics, The Pennsylvania State Un ...
Multiple Knockout Analysis of Genetic Robustness in the Yeast
Multiple Knockout Analysis of Genetic Robustness in the Yeast

... results of multiple concurrent knockouts to the metabolic genes of S.cerevisiae, we provide the first large-scale study of metabolic network robustness, portraying its architecture and shedding new light on its evolution. 1000-word abstract Genetic robustness characterizes the constancy of the pheno ...
Work Day 2
Work Day 2

... a mutation because of a replication error. __ Mutant gyrase enzyme is altered, allowing for DNA synthesis to occur even in the presence of ciprofloxacin. __ Mutant gyrA DNA is transcribed. ...
Modern theory of evolution o Bottleneck Mutation
Modern theory of evolution o Bottleneck Mutation

... Selects against extremes. Acts to eliminate both extremes from the phenotypes; individuals at the center of the curve show highest fitness. q Ex: babies born to humans tend to be around the same size and birth weight. Larger and smaller infants are not as fit. In ducks and chickens eggs those with i ...
Third HANDOUT
Third HANDOUT

... (left) and PstDC3000(avrRpt2) (right). Plants were inoculated by dipping them into bacterial suspensions (3 to 5 × 10 8 CFU/cm 2 ) containing the surfactant Silwet L77. B, Growth of PstDC3000 and PstDC3000(avrRpt2) in leaf tissue of Col-0 rps2, No-0 rps2, and No-0 RPS2 plants.. In B, A. thaliana pla ...
Dihybrid Crosses
Dihybrid Crosses

... homozygous for both of the normal traits, what would be the phenotypes and genotypes of their progeny? If the F1 generation was allowed to mate randomly among themselves, what phenotypes and genotypes would be expected among the F2’s, and in what proportions? ...
Human Genome Project - the Centre for Applied Genomics
Human Genome Project - the Centre for Applied Genomics

... percent of the dna scattered throughout the three billion nucleotides of genetic information. To complicate matters, human genes almost always appear as discontinuous segments of dna along a chromosome divided into gene-coding regions (exons) and noncoding regions (introns) (Figure 6). To complicate ...
Document
Document

... known to be bound by two TFs (ChIP-on-chip data and literature evidences), the authors made predictions of their corresponding TF binding sites and examined the relationship between these two sites on the promoter sequences. The sequence relationships between the binding motifs were examined in term ...
BIOLOGY Cells Unit GUIDE SHEET
BIOLOGY Cells Unit GUIDE SHEET

... 14. Explain why frameshift mutations (mutations involving the insertion of deletion of one or more nucleotides in a gene) usually have major effects on the amino acid sequence of a protein (page 199). ...
Albinism Powerpoint
Albinism Powerpoint

...  Causes eyes to appear pink as well as ...
Conserved amino acid sequences confer nuclear localization
Conserved amino acid sequences confer nuclear localization

... amplification of the entire gene in two fragments that overlapped in the second intron region. Primers for the 5V and 3V ends of the gene were based upon bovine gene sequences (Showalter et al., 2002). The 3510 bp oProp1 gene has three exons and two introns (Fig. 1A), a structure similar to that of ...
- Wiley Online Library
- Wiley Online Library

... et al. 2009). Indeed, genetic studies confirmed this hypothesis by identifying mutations in four genes all encoding components of the ciliary intraflagellar transport complexA (IFT122, WDR35, C14ORF179, and WDR19) (Gilissen et al. 2010; Walczak-Sztulpa et al. 2010; Arts et al. 2011; Bredrup et al. 2 ...
Chapter 10
Chapter 10

... 10.1 Meiosis, Genes, and Alleles 1. How does the term gene relate to the term allele? Genes are a segment of DNA with the necessary information to code for a protein and regulate its expression and are at specific locations on chromosomes. The many forms a gene can have are referred to as its allele ...
Genetics and Inheritance - Harford Community College
Genetics and Inheritance - Harford Community College

... 100 births and with African-Americans, the rate is greater (1 in 77) • Fraternal twins are created when two eggs are released and fertilized at the same time. May or may not be the same gender. • Identical twins are produced when the fertilized zygote cells split apart during development. The offspr ...
DNA - NIU Department of Biological Sciences
DNA - NIU Department of Biological Sciences

... that are spliced out of the messenger RNA. Only mutations within genes can affect the organism. Base substitution mutations within a gene can alter or destroy the gene’s protein product. The protein may not function at all, or it might be less efficient, or it might have an altered pH optimum or tem ...
QuASI: Question Answering using Statistics, Semantics, and
QuASI: Question Answering using Statistics, Semantics, and

... expand the original set, and increase recall. • Some rules with lower confidence get a lower weight in the ranking step. ...
Is DNA methylation of tumour suppressor genes epigenetic? The
Is DNA methylation of tumour suppressor genes epigenetic? The

... modes of action are analogous to those of histone acetylases and other chromatin-modifying activities that are involved in transcriptional regulatory mechanisms (Struhl, 1998). In particular, classical transcriptional activation and repression mechanisms involve the targeted recruitment of chromatin ...
DNA Is The Stuff Of Life
DNA Is The Stuff Of Life

... hereditary information to the next generation. Because of his professional stature in biology, this concept focused the work of others toward the nucleus. The next milestone in determining the nature of the hereditary information was performed by Friedrich Miescher. He studied pus cells that he coll ...
Chapter 19. - Kenston Local Schools
Chapter 19. - Kenston Local Schools

...  bonds tightly to brain protein, HAP-1 ...
A Parkinson Disease Gene Discovered, an
A Parkinson Disease Gene Discovered, an

... the gene and its protein.” “We cloned the cDNA of DJ-1 and reported in 1997 that DJ-1 is a novel oncogene in collaboration with ras,” says Ariga. Before the PD discovery, Ariga says their DJ-1 research focused on the roles in cancer and reproduction. In some instances of male infertility, Ariga expl ...
Biotechnology
Biotechnology

... open the cells and denature their DNA; the resulting single-stranded DNA molecules are treated so that they stick to the filter. ...
Using CRISPR-Cas9 to eradicate antimicrobial resistance genes
Using CRISPR-Cas9 to eradicate antimicrobial resistance genes

... resort ineffective. It has been postulated that we are entering a post-antibiotic era where even simple infections might be fatal, and routine medical procedures that depend of antibiotic prophylaxis will be impossible. Discovering ways to prevent or even reverse the spread of AMR would be truly gro ...
Population Genetics and a Study of Speciation Using Next
Population Genetics and a Study of Speciation Using Next

... from both ends of a larger fragment, and information about the distance between these sequences is retained. Longer reads from Sanger and 454 sequencing were used to assemble the accessory gland transcriptome of crickets de novo (from scratch). They generated enough of these sequencing reads to cove ...
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Site-specific recombinase technology



Nearly every human gene has a counterpart in the mouse (regardless of the fact that a minor set of orthologues had to follow species specific selection routes). This made the mouse the major model for elucidating the ways in which our genetic material encodes information. In the late 1980s gene targeting in murine embryonic stem (ES-)cells enabled the transmission of mutations into the mouse germ line and emerged as a novel option to study the genetic basis of regulatory networks as they exist in the genome. Still, classical gene targeting proved to be limited in several ways as gene functions became irreversibly destroyed by the marker gene that had to be introduced for selecting recombinant ES cells. These early steps led to animals in which the mutation was present in all cells of the body from the beginning leading to complex phenotypes and/or early lethality. There was a clear need for methods to restrict these mutations to specific points in development and specific cell types. This dream became reality when groups in the USA were able to introduce bacteriophage and yeast-derived site-specific recombination (SSR-) systems into mammalian cells as well as into the mouse
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