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Supplementary Information (doc 83K)
Supplementary Information (doc 83K)

... pomeroyi and Rhizobium leguminosarum respectively. These media either contained or lacked 5 mM DMSP. The cells were assayed for -galactosidase activity essentially as described by Rossen et al. (1985). The effects of the putative regulatory gene SPO0454 on the expression of the dddW-lacZ and the SP ...
Syllabus P140C (68530) Cognitive Science
Syllabus P140C (68530) Cognitive Science

... • Network can learn to associate output patterns with input patterns by adjusting weights • Hidden units tend to develop internal representations of the input-output associations ...
(2 pts). - nslc.wustl.edu
(2 pts). - nslc.wustl.edu

... The chi-square is not significant, so we cannot reject the null hypothesis of neutrality (1 pt). b. Test the null hypothesis of no selection on this gene using the Old/Young classification test. If significant selection is detected, identify whether or not it is conservative (negative) or directiona ...
1. Which genetic concept was proposed by Mendel?
1. Which genetic concept was proposed by Mendel?

... Genes from their father are stronger than genes from their mother, so the genes from their mother are not expressed. ...
Practical Issues in Microarray Data Analysis
Practical Issues in Microarray Data Analysis

... No systematic errors – only random noise In fact systematic error is almost as great as random noise in many microarray experiments ...
Presentation - University of Warwick
Presentation - University of Warwick

... The pancreas is responsible for regulating blood glucose levels. It contains hundreds of colonies of cells within the exocrine tissue, consisting predominately of β-cells, the main source of insulin within the body. Mouse models have been created with the chimeric c-MycERTAM gene active in the pancr ...
lab_july26_delong - C-MORE
lab_july26_delong - C-MORE

... Automa tic training of gene finding parameters for new bac terial genomes using only genomic DNA as an i nput (optionally, pre-learned parame ters from r elated organism can be used) ...
CYTOGENETICS AND MEDICAL GENETICS IN THE 1960s
CYTOGENETICS AND MEDICAL GENETICS IN THE 1960s

... embryonic fibroblasts, they first identified the correct number of chromosomes to be 46. ...
A reliable and efficient method for deleting
A reliable and efficient method for deleting

... We wanted to use homologous recombination in bacteria as a rapid, reliable tool to make a precise deletion of the enhancer located upstream of the human renin gene located on a PAC (14). For this purpose, we obtained a PAC from Genome Systems with a 160 kb insert containing the human renin gene, 75 ...
1. Data Distributions
1. Data Distributions

Problem Set V - Biology 2970
Problem Set V - Biology 2970

... a) Assuming that the T(14;21) chromosome and the normal 14 and 21 form a trivalent in prophase I and that two-from-one segregations always occur in anaphase I, determine what chromosomal types of progeny would be produced by the parents described above. b) Since the only children born to parents of ...
Genetics Unit Review Guide
Genetics Unit Review Guide

... 20) Explain the difference between sex influenced and sex linked inheritance and give an example of each. 21) Know what it means to be a carrier of a disorder, what types of disorders this works for (or doesn’t) and what gender of individuals can be carriers for particular traits. 22) Know how calcu ...
Document
Document

... the committee assigned to determine whether Santhi is female. Here are possible results of the initial tests (we don’t know the real results): Female genitalia: Yes Breasts and pubic hair: Yes Regular menstrual cycle: Never ...
Hands On - Gene Prediction in Prokaryotes file
Hands On - Gene Prediction in Prokaryotes file

... This step follows after the genome of a species has been sequenced. In general, the process includes identifying protein-coding regions, RNA genes, and regulatory regions. The three major categories of gene prediction algorithms are alignment-based, sequence-based, and content-based. Some algorithms ...
Detailed Methods: Supplementary Information
Detailed Methods: Supplementary Information

... The Ct values for each sample were averaged to obtain raw Ct values in Microsoft Excel and transformed into relative quantification data using the deltaCt method. To perform deltaCt analyses, we first subtracted the highest Ct value from all other Ct values for each gene measured such that the high ...
Expressed Sequence Tags: Any Prior Art Effect?
Expressed Sequence Tags: Any Prior Art Effect?

... suggest its homologs because homologs often have similar properties and therefore chemists of ordinary skill would ordinarily contemplate making them to try to obtain compounds with improved properties. Similarly, a known compound may suggest its analogs or isomers, either geometric isomers . . . or ...
Name - Humble ISD
Name - Humble ISD

... 1. Nondisjunction - Abnormal numbers of chromosomes in _gametes________ result in genetic disorders called _number disorders_____. This must often is a result of _nondisjunction___, which means _”not coming apart”___. In nondisjunction, a chromosome pair fails to separate correctly in _anaphase_____ ...
Gene Section BCL2L14 (BCL2-like 14 (apoptosis facilitator)) Atlas of Genetics and Cytogenetics
Gene Section BCL2L14 (BCL2-like 14 (apoptosis facilitator)) Atlas of Genetics and Cytogenetics

Chromatin signature reveals over a thousand highly conserved
Chromatin signature reveals over a thousand highly conserved

... array. The samples included the original four cell types (mouse ESCs, NPC, MEF and MLF), a time course of embryonic development (whole embryo, hindlimb and forelimb at embryonic days 9.5, 10.5 and 13.5), and four normal adult tissues (brain, lung, ovary and testis) (Supplementary Fig. 5 and Suppleme ...
Supplemental File S3. Homologous Chromosomes
Supplemental File S3. Homologous Chromosomes

... The human X and Y chromosomes are hypothesized to have evolved from homologous autosomes into the dimorphic sex chromosomes they are today (11-17). Vertebrates employ different mechanisms of sex determination: not all vertebrates have X and Y chromosomes, many vertebrates do not have sex chromosomes ...
Bone,  14,  347-352,  (1993)
Bone, 14, 347-352, (1993)

... In primary cultures, an apparently homogeneous population of proliferating calvarial-derived cells progressively differentiates into cells with a characteristic osteocytic morphology within multilayered nodules exhibiting a bone tissue-like organization. It is, therefore, necessary to determine at t ...
A Novel Deletion Mutation of Exon 2 of the C19orf12 Gene in an
A Novel Deletion Mutation of Exon 2 of the C19orf12 Gene in an

... Mutations in the C19orf12 gene are known to cause mitochondrial membrane proteinassociated neurodegeneration (MPAN), which is a neurodegeneration with brain iron accumulation (NBIA) type 4 disorder. To the best of our knowledge, this is the first report of a genetically confirmed case of MPAN from O ...
function Complex genomic rearrangements lead to novel primate gene
function Complex genomic rearrangements lead to novel primate gene

... (Fig. 1A). The N-terminal leucine-rich region is followed by RanGTP-binding domains (RanBP1 homologous domains or RBD) related to the one present in RanBP1, a variable number of zinc-finger motifs, and a C terminus with homology to cyclophilin A (Fig. 1A). In addition to the human RanBP2 ortholog, w ...
Introduction to Genetics - Cherokee County Schools
Introduction to Genetics - Cherokee County Schools

... Assortment says that the alleles separate during meiosis independent from each other  Thomas Hunt Morgan identified that genes on the same chromosome would move together – they are “linked” ...
lecture 21
lecture 21

... by mobile elements and their large contribution to the total mutation pool some insertions will be advantageous (due to changes in coding or regulatory sequences) Also plenty of examples (mostly in bacteria) of antibiotic (or other resistance) conferred by mobile elements carried in plasmids ...
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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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