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ppt - Sol Genomics Network
ppt - Sol Genomics Network

... Tries to find ‘full’ open reading frames in aligned UniGenes Automatic generation of gene predictor training set Parameters? ...
Analysis of RNA-seq Data.pptx
Analysis of RNA-seq Data.pptx

... A lot of orthologous genes share same domains A lot of TF also share DNA-binding domains, same sequence in there A gene from this domains will map to domains of other genes too Copy number increase will also cause multi-reads ...
Part C: Genetics
Part C: Genetics

... Each set of chromosomes, one set inherited from each parent, contains one copy of each gene. Depending on the alleles inherited, this will dictate the physical appearance or phenotype of an individual. The actual combination of genes received from each parent is known as the genotype. If one version ...
Project : Operon Prediction - Bioinformatics at School of Informatics
Project : Operon Prediction - Bioinformatics at School of Informatics

... Certain operons, particularly those that encode subunits of multiprotein complexes (e.g. ribosomal proteins) are conserved in phylogenetically distant bacterial genomes. ...
GENE`S INTERACTIONS
GENE`S INTERACTIONS

... In regard to anemia, the Hb(A) allele is obviously dominant. In regard to blood cell shape, however, there is incomplete dominance. Finally, as we shall now see, in regard to hemoglobin itself there is codominance. The alleles Hb(A) and Hb(S) actually code for two different forms of hemoglobin and b ...
Gene Section MLLT7 (myeloid/lymphoid or
Gene Section MLLT7 (myeloid/lymphoid or

... TTGTTTAC. Target genes: Akt, AFX is able to induce Rb-independent, p27kip1-mediated G1-arrest. Phosphorylation of AFX by protein kinase B inhibits its transcriptional activity. ...
Lecture7
Lecture7

... respect to amino acids in proteins • As a result, it was incorrectly assumed that the triplets encoding for amino acid sequences form contiguous strips of information. ...
Document
Document

... Use a Punnett square to show the offspring of a cross between two pea plants that are heterozygous for height (Tt). Give the phenotype and genotypes of the offspring. (That is, what is the phenotypic and genotypic ratios!) Use a Punnett square to show the offspring of a cross between a pea plant tha ...
There are a number of ways to find genes and gene information in
There are a number of ways to find genes and gene information in

... there will be multiple NM numbers. Now let’s consider the function of the gene you are studying. There are many ways to find out the function but one of the easiest for getting started is to look at the summary provided. This will usually tell you a bit about the function and a bit about other membe ...
14) basic genetic concepts - University of Wisconsin–Madison
14) basic genetic concepts - University of Wisconsin–Madison

... For 29 of the chromosome pairs, both members are visually identical. However, for one of the pairs, one member is much longer; it is called the X chromosome, and the shorter member is called the Y chromosome. All the ova carry the X chromosome, but the spermatozoa can carry either the X or the Y chr ...
Mendel`s Legacy
Mendel`s Legacy

... affected gene (dominant or recessive) leads to the condition. - Familial hypercholesterolemia (FH) – is a condition that affects heterozygotes (1:500). The cell produces less receptors for LDL (lipids) that are required to take these lipids into the cell. Without them these lipids build up in the ar ...
PowerPoint
PowerPoint

...  Animation w/ narration, same style as mitosis ...
How to Make a Linkage Map
How to Make a Linkage Map

... How to Make a Linkage Map  Independent assortment occurs when genes/ chromosomes separate from each other independently  during meiosis and therefore are inherited separately from each other. This is true if the genes for the  observed phenotypes are found on different chromosomes or separated by la ...
Add Meiosis Vocabulary to notes
Add Meiosis Vocabulary to notes

... Chromatids: the two halves of a chromosome; half original, half rebuilt ...
Unit 3
Unit 3

... Random joining of gametes: which sperm fertilizes which egg is to a large degree a random event. In many cases, however, this event may be affected by the genetic composition of a gamete. For example, some sperm may be faster swimmers and have a better chance of fertilizing the egg. It is important ...
b230 - IPB Repository - Bogor Agricultural University
b230 - IPB Repository - Bogor Agricultural University

... transfer each of these genes to B. japonicum strains. Mating was conducted on membrane filter (0.45 gm, Millipore) using modified Luria Agar. The results showed that all of the genes were able to be transferred to acid tolerant B. japonicum strains by conjugation. All of these bacteria were able to ...
Biology of Laboratory Rodents
Biology of Laboratory Rodents

... – DNA sequence that encodes for a specific protein product – gene “expression” means protein product is being made via transcription and translation (DNA to RNA to protein) ...
Mendelian Genetics
Mendelian Genetics

... Law of Segregation • 3. When gametes (sex cells) are produced, allele pairs separate or segregate leaving them with a single allele for each trait. • 4. When the two alleles of a pair are different, one is dominant and the other is recessive. ...
genetics notes kelly
genetics notes kelly

... Basedon Mendialian genetics and probability rules Tests for identifying carriers Fetal testing Newborn screening CARRIER = Heterozyous individual that doesn’t show trait, but can pass it on to offspring ...
Lecture 40_GeneRegulationI_transcriptional_control_RoadMap
Lecture 40_GeneRegulationI_transcriptional_control_RoadMap

... • Prokaryotic genes are often grouped together into “operons,” which contain multiple genes under the same control system/sequences • The lac operon is the genetic locus that allows E. coli to metabolize lactose (if no glucose is around – glucose is the preferred source) • Contains promoters, operat ...
GENETICS 310
GENETICS 310

... Meisois I configuration ...
Year 13 Biology - miss-lovell-presents
Year 13 Biology - miss-lovell-presents

... 12. Albinism is a disease which has a pleiotropic effect. What is meant by this term? 13. Certain genes have the ability to suppress the expression of a gene at a second locus. In pumpkin, colour is recessive to no colour at one allelic pair. This recessive allele must be expressed before the specif ...
NeuroAnatomic and Genetic Approaches to Memory Formation
NeuroAnatomic and Genetic Approaches to Memory Formation

... Gene replacement and transgenic animals • Some genes are identified through mutant analysis Forward Genetics (mutant phenotype---> genotype) • To determine the function of these genes, it is possible to replace an organism’s wild type gene with an inactive gene to create a “gene knockout” Reverse G ...
MENDEL=S HYPOTHESES TO EXPLAIN INHERITANCE
MENDEL=S HYPOTHESES TO EXPLAIN INHERITANCE

... According to this idea, the F1 hybrids had green pods because the allele for the trait is dominant over the allele for yellow pods, which is recessive. ...
Ch 15 summary - OHS General Biology
Ch 15 summary - OHS General Biology

... Because males have only one locus, the terms homozygous and heterozygous lack meaning for describing their X-linked genes. o The term hemizygous is used in such cases. The chance of a female inheriting a double dose of the mutant allele is much less than the chance of a male inheriting a single dose ...
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Genomic imprinting

Genomic imprinting is the epigenetic phenomenon by which certain genes are expressed in a parent-of-origin-specific manner. If the allele inherited from the father is imprinted, it is thereby silenced, and only the allele from the mother is expressed. If the allele from the mother is imprinted, then only the allele from the father is expressed. Forms of genomic imprinting have been demonstrated in fungi, plants and animals. Genomic imprinting is a fairly rare phenomenon in mammals; most genes are not imprinted.In insects, imprinting affects entire chromosomes. In some insects the entire paternal genome is silenced in male offspring, and thus is involved in sex determination. The imprinting produces effects similar to the mechanisms in other insects that eliminate paternally inherited chromosomes in male offspring, including arrhenotoky.Genomic imprinting is an inheritance process independent of the classical Mendelian inheritance. It is an epigenetic process that involves DNA methylation and histone methylation without altering the genetic sequence. These epigenetic marks are established (""imprinted"") in the germline (sperm or egg cells) of the parents and are maintained through mitotic cell divisions in the somatic cells of an organism.Appropriate imprinting of certain genes is important for normal development. Human diseases involving genomic imprinting include Angelman syndrome and Prader–Willi syndrome.
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