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Supplementary Discussion References
Supplementary Discussion References

... performed according to Codelink protocol (GE Amersham Biosciences). In brief, 2 µg of total RNA from each DLPFC sample was transformed into cDNA by reversetranscription, cleaned on a column, and synthesized to biotinylated cRNA by in vitro transcription which made up to 50 µg of cRNA. The unfragmen ...
Paraneoplastic Antigen-Like 5 Gene (PNMA5) Is
Paraneoplastic Antigen-Like 5 Gene (PNMA5) Is

... were determined based on the Nissl staining patterns of the adjacent sections. The images of the ISH-stained sections of PNMA5 and RBP were then transformed using Adobe Photoshop, so that the heights of the images became equal. The optical density of the adjusted images was measured using ImageJ im ...
1 The Transformations of Darwinism
1 The Transformations of Darwinism

... a struggle for existence. By using these laws, it is possible to formulate Darwin’s theory in a very general and abstract way, without referring to our own world or to the types of reproduction, inheritance, variation, and competition with which we are familiar. For example, in British evolutionary ...
Computational Biology
Computational Biology

... more common than fusions and fissions. Therefore use as a rule always to select reversals/translocations before fusions/fissions. Often, the list of good reversals contains nonoverlapping reversals, and the order in which these reversals are performed is often irrelevant. Compute for each good rever ...
LOSS OF HETEROZYGOSITY DUE TO SHORT-TRACT AND LONG-TRACT SACCHAROMYCES CEREVISIAE Thomas Coates
LOSS OF HETEROZYGOSITY DUE TO SHORT-TRACT AND LONG-TRACT SACCHAROMYCES CEREVISIAE Thomas Coates

... (Ingvarsson, 2001). Overlapping in sequence with the FHIT gene is the large (~4Mb) CFS FRA3B, notable as being the most commonly broken in lymphocytes (the cell type traditionally used in CFS research) and first characterised CFS (Durkin and Glover 2007; Smith et al., 2006). Loss of the functionalit ...
The Classical Genetic Switch in Lambda Phage- Lysis and
The Classical Genetic Switch in Lambda Phage- Lysis and

... made and it activates its own transcription from PRM. This switches OFF the other phage genes including CII. Thus we see the establishment of lysogeny in lambda phage, even in the absence of the inducer signal. ...
The formal Darwinism project: a mid
The formal Darwinism project: a mid

... an optimization programme on the other. To capture the whole of Darwin’s argument, these formal links must be made as general as possible, in a number of ways. Genetic architecture is vital to the equations of motion, but secondary to the concept of natural selection – after all Darwin knew nothing ...
Cluster Analysis for Gene Expression Data
Cluster Analysis for Gene Expression Data

... However, for gene expression data, patterns’ similarity seems more important than their spatial distance. Pearson correlation coefficient is also widely used to measure the strength of the linear relationship between two objects. This measure has the advantage of calculating similarity depending onl ...
Series 1: Cross Diagrams There are two alleles for each trait in a
Series 1: Cross Diagrams There are two alleles for each trait in a

... dpy unc dpy unc ...
Novel Function of the Eukaryotic Polypeptide
Novel Function of the Eukaryotic Polypeptide

... Abstract—The mammalian GTP-binding protein GSPT, whose carboxy-terminal sequence is homologous to the eukaryotic elongation factor EF1α, binds to the polypeptide chain releasing factor eRF1 to function as eRF3 in translation termination. However, the amino-terminal domain of GSPT, which contains a p ...
Communique of GTTAC Meeting 18 September 2003 and 28
Communique of GTTAC Meeting 18 September 2003 and 28

Inheritance Lecture Notes - Instruction.greenriver.edu
Inheritance Lecture Notes - Instruction.greenriver.edu

... 60m hurdles the next day but she wasn't sure if she would be able to compete. Earlier that day she reported to "Sex Control" which scraped cells from her cheek to test for sex chromosomes. She had passed the test in 1983 in Helsinki but had forgotten to bring her "Certificate of Femininity". A few h ...
a hint of the same genetic defect as in Fechtner syndrome
a hint of the same genetic defect as in Fechtner syndrome

... Autosomal-dominant giant platelet disorders are rare. The most prevalent diseases that belong to this entity are May-Hegglin anomaly, Fechtner syndrome, Sebastian platelet syndrome, and Epstein syndrome. Fechtner syndrome, first described in 1985 by Peterson et al,1 is an autosomal-dominant variant ...
Diagnostic and Prognostic Significance of Gene Expression
Diagnostic and Prognostic Significance of Gene Expression

... normally down-regulated in the GC where apoptosis plays a critical role in negative B-cell selection • t(14;18)  fusion gene leading to transcription of  levels of BCL2 ...
Communique of GTTAC Meeting 18 September 2003 and 28
Communique of GTTAC Meeting 18 September 2003 and 28

... bacterium, which encodes an insecticidal protein (VIP3A) that is toxic to lepidopteran caterpillar pests of cotton. It also contains a bacterial gene hph, conferring resistance to hygromycin, an antibiotic that was used as a selectable marker in the initial laboratory stages of developing the GM cot ...
Module 4: The Role of Genes in Cancer
Module 4: The Role of Genes in Cancer

... Gene mutations can be either acquired, or inherited from a parent. Changes in DNA that develop throughout a person's lifetime are acquired mutations. Acquired mutations cannot be passed on by individuals to their children. Common disorders such as heart disease, diabetes, and most cancers arise from ...
Slide 1
Slide 1

...  Portion of DNA that provides the instructions for making ...
REPORT Molecular Cytogenetic Analysis and Resequencing of Contactin Associated Protein-Like 2
REPORT Molecular Cytogenetic Analysis and Resequencing of Contactin Associated Protein-Like 2

... We evaluated both cases and controls in the identical fashion in search of rare nonsynonymous, frame-shift, nonsense, and splice-site variants. Those changes that were found only in the case or the control group in the initial sequencing effort were further genotyped with Custom Taqman Genotyping as ...
Morphogenesis of Flowers—Our Evolving View
Morphogenesis of Flowers—Our Evolving View

... 1994), although resolution is still not in sight. Two alternative schemes were proposed early: the euanthial theory, in which flowers arose de novo, and the pseudanthial theory, in which they arose through the combination of originally separate female and male inflorescence shoots. The main difficul ...
What is heritability?
What is heritability?

... inheritance of such traits is relatively easy to predict, and the different phenotypes tend to occur in qualitatively distinct states (such as "black" and "red"). Other traits, usually called quantitative traits, may be influenced by many different genes, and the continuous variation observed often ...
Ch 13 outline
Ch 13 outline

... The number of combinations possible when chromosomes assort independently into gametes is 2n, where n is the haploid number of the organism.  If n = 3, there are 23 = 8 possible combinations.  For humans with n = 23, there are 223, or more than 8 million possible combinations of chromosomes. ...
Genetic Imprinting in Maize Bhavani P1*, Harinikumar K. M1
Genetic Imprinting in Maize Bhavani P1*, Harinikumar K. M1

... progeny (Agrawal et al., 1999) has opened up a new dimension of this, much ignored theory of science. The term “epigenetics” was first coined by Waddington (Waddington, 1942), which literally means “above stress”. Waddington defined epigenetics as “environment-gene interactions that induce developme ...
File
File

... This topic reveals the source of genetic variation. That is the source of variation on which natural selection acts. The random orientation, cross-over and mutation are random processes. The natural selection of a particular phenotype is not. This topic requires us to regard sexually reproducing pop ...
Unexpected requirements for neural induction in the
Unexpected requirements for neural induction in the

... The molecular mechanism underlying neural induction became clear when binary protein complexes between BMP4 and Chordin, BMP4 and Noggin, and Follistatin and BMP7 were found2. These observations suggest that the function of a neural inducing factor is to remove free BMP proteins from the area around ...
Computability and Learnability of Weightless Neural Networks
Computability and Learnability of Weightless Neural Networks

... finite set. The tape is scanned in either left or right direction one cell at a time. A WNN, and any ANN, is a finite state automata. The only missing component for the equivalence is access to a tape in a similar fashion to Turing machines. This can be easily simulated by (de )coding instructions f ...
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Gene expression programming

In computer programming, gene expression programming (GEP) is an evolutionary algorithm that creates computer programs or models. These computer programs are complex tree structures that learn and adapt by changing their sizes, shapes, and composition, much like a living organism. And like living organisms, the computer programs of GEP are also encoded in simple linear chromosomes of fixed length. Thus, GEP is a genotype-phenotype system, benefiting from a simple genome to keep and transmit the genetic information and a complex phenotype to explore the environment and adapt to it.
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