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Geuvadis Analysis Meeting
Geuvadis Analysis Meeting

... - Quantified 615 datasets based on the Gencode v7 annotation - Sensitivity is a function of sequencing depth ...
Dell`Orphano: SNP discovery
Dell`Orphano: SNP discovery

PTC Assessment - Student Version
PTC Assessment - Student Version

... Q1: For a male guppy, what would be one a major advantage and one major disadvantaged of having very brightly colored tails in the wild? [Broad area 1.1] Scientists studying guppy behavior noticed that the females needed to be able to detect Ultra-Violet (UV) light to make decisions about the qualit ...
Unlocking my genome - Piner High Stem Cafe
Unlocking my genome - Piner High Stem Cafe

... serious blood clot, nor that I am cleared of worry about other diseases that didn't show up in my results. And there's always the risk I could overreact. One of my "Variants of Unknown Significance" is a mutation for Lynch syndrome, which predisposes me to certain kinds of cancers, according to my I ...
1 Today: Genetic and Physical Mapping Sept 2. Structure and
1 Today: Genetic and Physical Mapping Sept 2. Structure and

Characterization and transcript mapping of a bovine herpesvirus
Characterization and transcript mapping of a bovine herpesvirus

... sequencing strategies employed are shown in Fig. 1. The nucleotide sequence of fragment M has a G + C content of 72%, which agrees with previous estimates based on the whole viral genome ( G r a h a m et al., 1972). This high G + C content generates occasional nucleotide compressions in sequencing g ...
FISH
FISH

... imaging software, can distinguish all 23 chromosomes by chromosome specific colors. This type of analysis can be used to detect abnormalities that affect multiple chromosomes as is sometimes found in cancer cells or immortalized cell lines. ...
Lecture Presentation to accompany Principles of Life
Lecture Presentation to accompany Principles of Life

... rejoining, but segment is “flipped” Translocations—segment of DNA breaks off and is inserted into another chromosome; this can lead to duplications and deletions ...
A Recipe for Traits - Learn Genetics (Utah)
A Recipe for Traits - Learn Genetics (Utah)

... 5. Set the piece of DNA aside and repeat steps 1-4 for the next trait on the key. 6. After circling the matching picture, tape the second piece of DNA to the first to make one long strand. This will become the DNA recipe for your entire dog. 7. Repeat these steps for each of the traits listed on the ...
12.3 How Is Biotechnology Used In Forensic Science?
12.3 How Is Biotechnology Used In Forensic Science?

... farther toward the positive electrode. ...
Experimental procedures (detailed)
Experimental procedures (detailed)

... sequence similarities between ESTs of Plumbago zeylanica sperm cells and those of other gamete-related cells or organs, local tBLASTx searches were performed with a cut-off value of 1.0×e-10. ...
Lab: Colony PCR amplification of the 16S ribosomal RNA gene I
Lab: Colony PCR amplification of the 16S ribosomal RNA gene I

... Archaea. With the aid of the polymerase chain reaction (PCR), these strategies have greatly enhanced our ability to describe the genetic diversity of microorganisms in the natural environment without the need for cultivation. The cloning and sequencing of PCR-amplified SSU rRNA genes is now a routin ...
Environmental DNA-Encoded Antibiotics Fasamycins A and B Inhibit
Environmental DNA-Encoded Antibiotics Fasamycins A and B Inhibit

... Exploiting this genetic diversity should prove to be a useful strategy for uncovering new bioactive metabolites that can serve as novel therapeutics.4,5 The inability to culture many of the bacteria present within environmental samples renders these microbes incompatible with the most heavily relied ...
The Discovery and Significance of Selected Blood Groups
The Discovery and Significance of Selected Blood Groups

... Homozygosity by Descent (HBD) Gene Mapping • Genomic DNA from the 6 Jr(a‒) subjects was first analysed for SNPs on an array (Affymetrix GeneChip Human Mapping 250K NspI array) and then by HBD ...


The study of threshold determination of gene identification and its
The study of threshold determination of gene identification and its

... Firstly, this essay will discuss the threshold determination of different species types of genes. To determine the threshold of genes types in different species, and to study the threshold determination method of each kind of representative gene sequence exons, and determine the threshold. And throu ...
Document
Document

... – The remaining 98.5% of the DNA contains – Control regions such as promoters and enhancers – Unique noncoding DNA – Repetitive DNA – Found in centromeres and telomeres – Found dispersed throughout the genome, related to transposable elements that can move or be copied from one location to another C ...
Tasks for individual work in analytical chemistry for the 2d year
Tasks for individual work in analytical chemistry for the 2d year

... Characterization of non-indicators methods of the precipitation titration. The content, possibilities of the method, the end point determination. Ways of the end point determination in oxidation-reduction titration. Reversible and irreversible redox indicators, examples of their use, non-indicators ...
national unit specification: general information
national unit specification: general information

... It is essential that this Unit is delivered in such a way as to emphasise the key points about the structure of DNA and its function in the cell. Instruments of assessments should be designed with this in mind. It is recommended that assessment of this Unit is by completion of a holistic end of Unit ...
1989 Allen Award Address: The American Society of Human Genetics Annual Meeting, Baltimore.
1989 Allen Award Address: The American Society of Human Genetics Annual Meeting, Baltimore.

... subsequently discovered in humans, and it was these that were the main markers in pre-RFLP linkage studies. The first correlations between physical and genetic markers at the DNA level were carried out with bacteriophage X (Davis and Parkinson 1971). These papers describe the generation and physical ...
Structure and function of nucleases in DNA repair: shape
Structure and function of nucleases in DNA repair: shape

... motifs (Aravind and Koonin, 1998a). The structure revealed a novel fold, which consists of a five-stranded parallel b-sheet flanked by six a-helices. The strand order of the b-sheet is 21345. On one side of the bsheet, four phosphoesterase motifs form a cluster, which contains five invariant asparta ...
Comparison between the efficiency of liposome and
Comparison between the efficiency of liposome and

... PCR fragment chosen for amplification was extended within the open reading frame of the recombinant GFP; from 2156 bps into 2520 bps. PCR amplification was taken place using conventional thermal cycler (Eppendorf Master Cycler - USA). PCR super mix was divided into aliquots into individual PCR tubes ...
Chapter 20
Chapter 20

... Gel electrophoresis separates macromolecules on the basis of their rate of movement through a gel in an electric field. How far a DNA molecule travels while the current is on is inversely proportional to its length. A mixture of DNA molecules, usually fragments produced by restriction enzyme digesti ...
What is PCR? - Cobb Learning
What is PCR? - Cobb Learning

... Separate Alu fragments on 2% agarose gel… Use Chi-Square or Hardy Weinberg to calculate population frequency of (+,+), (+,-) and (-,-). ...
Mitochondriontoplastid DNA transfer: it happens
Mitochondriontoplastid DNA transfer: it happens

... and leaving open the possibility that it began in the nuclear compartment and was then transferred independently to the mitochondrial and plastid genomes (Iorizzo et al., 2012a). Moreover, within the carrot mitochondrial genome, DcMP is fragmented and scrambled into three pieces, two of which are 80 ...
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Bisulfite sequencing



Bisulphite sequencing (also known as bisulfite sequencing) is the use of bisulphite treatment of DNA to determine its pattern of methylation. DNA methylation was the first discovered epigenetic mark, and remains the most studied. In animals it predominantly involves the addition of a methyl group to the carbon-5 position of cytosine residues of the dinucleotide CpG, and is implicated in repression of transcriptional activity.Treatment of DNA with bisulphite converts cytosine residues to uracil, but leaves 5-methylcytosine residues unaffected. Thus, bisulphite treatment introduces specific changes in the DNA sequence that depend on the methylation status of individual cytosine residues, yielding single- nucleotide resolution information about the methylation status of a segment of DNA. Various analyses can be performed on the altered sequence to retrieve this information. The objective of this analysis is therefore reduced to differentiating between single nucleotide polymorphisms (cytosines and thymidine) resulting from bisulphite conversion (Figure 1).
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