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t - nslc.wustl.edu
t - nslc.wustl.edu

... mutating per unit time (only neutral mutations are allowed). This model assumes that when a nucleotide site mutates it is equally likely to mutate to any of the three other nucleotide states. Suppose further that mutation is such a rare occurrence that in any time unit it is only likely for at most ...
Kernels for gene regulatory regions
Kernels for gene regulatory regions

... start from a set of genes known to be similarly regulated, for example by clustering gene expression data, and search for over-represented short sequences in their proximal intergenic regions. Alternatively, some authors have proposed to represent each intergenic sequence by its content in short se ...
Table S1.
Table S1.

... Table S1 – Overview of prediction attributes 0. General remarks In order to make the attributes comparable between multiple CpG islands and windows of different sizes, most attributes are averages (or standard deviations, etc.) over the window of interest, standardized to a 1kb window. Variance stab ...
A molecular probe for Basidiomycota: the spermidine
A molecular probe for Basidiomycota: the spermidine

... Using the PCR conditions described above and the designed degenerate primers, it was possible to amplify DNA fragments of the predicted size from genomic DNA of all the Basidiomycota species tested (see Materials and methods), whose genomes have been sequenced or not, that represented the three subp ...
The ABCs of Genetic Testing
The ABCs of Genetic Testing

... have X-linked trait  Among pediatric inpatients, more than 25% have a genetic disorder  Over 1/3 pediatric deaths attributed to congenital anomalies – 17% of these due to chromosome abnormalities, and 12% due to some other recognized malformation syndrome ...
Genome engineering of mammalian haploid embryonic stem cells
Genome engineering of mammalian haploid embryonic stem cells

... was engineered to contain mammalian codon-optimized Cas9 under the control of a CAG promoter (Mali et al., 2013). To examine the efficiency of knockout of each gene, haploid ESCs were co-transfected with the Cas9 expression vector and a sgRNA vector targeting Tet1, Tet2 orTet3, along with a puromyci ...
Finding Patterns in Protein Sequence and Structure
Finding Patterns in Protein Sequence and Structure

... • In the Markov chain models we have considered so far, the probabilities do not depend on where we are in a given sequence • In an inhomogeneous Markov model, we can have different distributions at different positions in the ...
Inquiry into Life Twelfth Edition
Inquiry into Life Twelfth Edition

... – Core histones form a ball with DNA wrapped around the outside – H1 also lies on the outside of the nucleosome ...
Chapter 25.
Chapter 25.

... Chapter 25. ...
Finding Patterns in Protein Sequence and Structure
Finding Patterns in Protein Sequence and Structure

... • In the Markov chain models we have considered so far, the probabilities do not depend on where we are in a given sequence • In an inhomogeneous Markov model, we can have different distributions at different positions in the ...
Slide Presentation
Slide Presentation

... BGC Model is Accepted  While fitness selection cannot be ruled out, there is no process known that would explain a fitness advantage of increasing the GC content of mega-base regions by selecting localized clusters of GC SNPs.  Fitness selection cannot explain the correlation with recombination r ...
Transvection in 2012: Site-Specific Transgenes Reveal a
Transvection in 2012: Site-Specific Transgenes Reveal a

... widespread in the Drosophila genome (Bateman et al. 2012; Mellert and Truman 2012). Both groups of researchers used the phi-C31 system to integrate transgenes into specific genomic locations to look at the ability of one transgene to activate the expression of another, greatly increasing our knowledg ...
asSeq: A set of tools for the study of allele-specific RNA
asSeq: A set of tools for the study of allele-specific RNA

... We assume DNA genotype data are available, either from SNP array or DNA sequencing. It is possible to call SNPs or indels in exonic regions from RNA-seq data, but we do not consider such approach here. First we need to impute haplotype data in a larger number of SNPs, for example, the SNPs/indels fr ...
7.13 Experimental Microbial Genetics
7.13 Experimental Microbial Genetics

... migrate toward the anode (positive end) due to the negatively charged phosphates along the DNA backbone. The migration velocity is limited by the frictional force imposed by the gel matrix. While charge and/or size can affect the rate at which macromolecules will pass through the gel, the charge to ...
Evolution of genetic and genomic features unique to the human
Evolution of genetic and genomic features unique to the human

... represents computational and/or assembly error. The sample size of sequenced individuals can also be an impediment as an apparent HLS change may be polymorphic in only the human population. In addition, the lack of sufficient individuals from the other sequenced primates can make the ancestral state ...
Supplement: Sequence analysis of GMR-dRetMEN2B
Supplement: Sequence analysis of GMR-dRetMEN2B

... AE003683 maps to different sites within AE003683. There may be 2 inserts, one in 1st intron of Dh, the other 92 bp upstream of Crc, or a single P that induced a 10.4 kb deletion to remove Scm, SpdS, the 1st exon of Dh ...
Transposition - Pennsylvania State University
Transposition - Pennsylvania State University

... Evidence Mechanisms: DNA-mediated RNA-mediated ...
Protocols for 16S rDNA Array Analyses of Microbial
Protocols for 16S rDNA Array Analyses of Microbial

... DNA Microarray Analyses SigmaScreen (Sigma) or CMT-GAPS (Corning Inc., Corning, New York) coated slides for microarrays may be used for the DNA array hybridization experiments. One µl (100 pmol/µl) of the complementary primers containing a 15-mer poly T tail at the 5’-end is spotted on the slide. ...
Microbial diversity and virulence probing of five different body sites
Microbial diversity and virulence probing of five different body sites

... -What are the differences in taxonomic & functional diversity between and within body sites? ...
Phylogenetic Affinity of Mitochondria of Euglena
Phylogenetic Affinity of Mitochondria of Euglena

... DNA isolated from purified mitochondrial fractions of E. gracilis by several methods proved to consist mainly of short heterogeneous-sized linear fragments migrating at approximately 5 kb in agarose (Fig. 1A). However, quantitative hybridization with a mitochondrial DNA-specific probe confirmed the ...
The epigenetic basis of gender in flowering plants and mammals
The epigenetic basis of gender in flowering plants and mammals

... biallelic expression of imprinted growth promoters, or deletion of imprinted genes involved in growth inhibition or apoptosis, occur in many cancers, both hereditary and sporadic (reviewed in Refs 20,21). Overexpression of Igf2 occurs in a wide variety of cancers, suggesting a correlation of paterna ...
The Study of Genetics: A Historical Perspective Ross Edwards
The Study of Genetics: A Historical Perspective Ross Edwards

... show what was occurring. He realized that each plant must have two traits, one inherited from each parent (Mawer 2006). By crossing Aa with Aa we would achieve three different variations: AA (25%) , Aa (50%), and aa (25%). In addition to this, he found that by combining multiple trait pairs (i.e. Aa ...
Loss of Albino3 leads to the specific depletion of the light
Loss of Albino3 leads to the specific depletion of the light

... the ac29-3 allele) confers a more stringent acetate-requiring phenotype than the ac29-2 nonsense mutation, it was first necessary to create a haploid strain for the NIC7 ac29-3 mt chromosome. Such an ac29-3 strain was constructed by crossing the acy32 diploid to a green nic7 mt strain and identify ...
Validation and Replication
Validation and Replication

... Examples from our group We have utilised a number of different processes: Repeat the experiment in the same samples using a different methodology Repeat the experiment in the same samples using a different source of tissue but the same technique Include extra samples to increase robustness Assess d ...
Lecture 13 - WordPress.com
Lecture 13 - WordPress.com

... • Wheat is a hexaploid, the result of 3 different species producing a stable hybrid. There are thus 3 similar but slightly different genomes contained in the wheat genome, called A, B, and D. • Each genome has a single gene that affects kernel color, and each of these loci has a red allele and a whi ...
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Genomics

Genomics is a discipline in genetics that applies recombinant DNA, DNA sequencing methods, and bioinformatics to sequence, assemble, and analyze the function and structure of genomes (the complete set of DNA within a single cell of an organism). Advances in genomics have triggered a revolution in discovery-based research to understand even the most complex biological systems such as the brain. The field includes efforts to determine the entire DNA sequence of organisms and fine-scale genetic mapping. The field also includes studies of intragenomic phenomena such as heterosis, epistasis, pleiotropy and other interactions between loci and alleles within the genome. In contrast, the investigation of the roles and functions of single genes is a primary focus of molecular biology or genetics and is a common topic of modern medical and biological research. Research of single genes does not fall into the definition of genomics unless the aim of this genetic, pathway, and functional information analysis is to elucidate its effect on, place in, and response to the entire genome's networks.
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