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Solution
Solution

... (1  point  each  for  accurate  contig  and  scaffold  definition,  1  point  for  correctly  described  paired   end  reads  connecting  contigs  into  scaffolds.)  A  contig  is  sequence  assembled  from  contiguous   or  overlapping  DN ...
oL-Amylase of Clostridium thermosulfurogenes EMi:
oL-Amylase of Clostridium thermosulfurogenes EMi:

Southern Blotting and Related DNA Detection Techniques
Southern Blotting and Related DNA Detection Techniques

... The system shown in Figure 1 is an accurate description of Southern blotting as still carried out in many laboratories, but various modifications have been introduced over the years to improve the efficiency of DNA transfer from gel to membrane. The major improvement has been the introduction of nylon ...
Proposed Changes to the NIH Guidelines for Research Involving
Proposed Changes to the NIH Guidelines for Research Involving

... 1)No more than half of the eukaryotic viral genome is present OR 2)There is a complete deletion in one or more essential viral capsid, envelope, or polymerase genes required for cell-to-cell transmission of viral nucleic acids and the investigator provides the IBC with evidence such as sequence or o ...
Environmental and Pollution Microbiology Exam 3 Review, LYoung
Environmental and Pollution Microbiology Exam 3 Review, LYoung

... 17. Understand the basic process of conjugal plasmid transfer via conjugation (F pilus, conjugation bridge, strand nicking at oriT, rolling circle replication) 18. Understand how Hfr strains are produced. Understand plasmids that can function as episomes and the importance of insertion sequences in ...
Comp 5a Packet
Comp 5a Packet

... actually "unzip" when it needs to replicate - or make a copy of itself. DNA needs to copy itself when a cell divides, so that the new cells each contain a copy of the DNA. Without these instructions, the new cells wouldn't have the correct information. The hydrogen bonds are represented by small cir ...
analysis of gene function
analysis of gene function

...  Because Cre recombinase can recognize and cut sequence LoxP (34bp) for achieving precise genetic manipulation in mice. Many of these desired genetic manipulations rely on Cre's ability to direct spatially and temporally specified excision of a pre-designated DNA sequence that has been flanked by d ...
questions - University of Saskatchewan Library
questions - University of Saskatchewan Library

... b) Pyruvate oxidation and oxidative phosphorylation c) Glycolysis and the citric acid cycle d) Pyruvate oxidation and the citric acid cycle 16. Suppose you have a cell sample that has a disorder that causes normal Okazaki fragments to be built during DNA replication but they are not linked together ...
Forensic DNA Analysis and the Validation of Applied Biosystems
Forensic DNA Analysis and the Validation of Applied Biosystems

Inheritance of Organelle DNA Sequences in a Citrus–Poncirus
Inheritance of Organelle DNA Sequences in a Citrus–Poncirus

... shown). Because paternal parents of openpollination progeny are unknown, a specific model for segregation of the P. trifoliata atpA configuration could not be tested. However, the segregation of both ...
Dharmacon Solutions for Studying Gene Function
Dharmacon Solutions for Studying Gene Function

ANSWER KEY
ANSWER KEY

... Acinetobacter calcoaceticus. You have purified a plasmid that contains the lacZ gene with the gene for kanamycin resistance inserted into the middle of the gene to inactivate it. You mix naturally competent culture of bacteria with a solution of plasmid DNA that has been treated in the following way ...
Click to
Click to

... ABSTRACT: Advances in genomics are leading to a new revolution in pigeonpea hybrid breeding, as these inventions facilitate the study of genotype and its relationship with the phenotype. The draft genome sequence of pigeonpea and Next Generation Sequencing (NGS) technologies has made it possible to ...
Mining the Human Genome Using Protein Structure Homology
Mining the Human Genome Using Protein Structure Homology

... P-value is calculated for alignment ensemble using distribution of scores The inverse of the P-value is reported ...
Next-Generation Sequencing applied to aDNA
Next-Generation Sequencing applied to aDNA

... The first line specifies that the name of this project is “Przewalski”. This means that all resulting files will start with “Przewalski”. The second line defines the sample name; this is used to tag the resulting alignments data, and is typically the same as the project name. The third line names a ...
Is DNA methylation of tumour suppressor genes epigenetic? The
Is DNA methylation of tumour suppressor genes epigenetic? The

060506-Meeting
060506-Meeting

... Project Goal ...
PDF
PDF

... Zizania, and those that are Zizania-specific genes (Figure 1b). As expected, Zizania appears to share more orthologous groups with Oryza (742 orthologous groups) than with Brachypodium or Sorghum; this finding is consistent with the phylogenetic tree based on their orthologous single-copy gene group ...
presentation - Harlem Children Society
presentation - Harlem Children Society

... Two separate ligations are done here; the first one is to insert the mut Hbraf into our constructed plasmid and the next ligation is to insert the wt Hbraf into our constructed plasmid without the mut Hbraf. Transformation is prepared with both newly constructed plasmids thus 62.1mod/oli/Trp2+mutH a ...
HEPATITIS B VIRAL (HBV DNA), QUANTITATIVE
HEPATITIS B VIRAL (HBV DNA), QUANTITATIVE

... Sample provided does not contain HBV DNA HBV DNA detected, but below the lower limit of linear range of the assay. These results should be interpreted with caution HBV DNA detected within the linear range of the assay HBV DNA detected above the linear range of the assay ...
Assessing the Homogeneity of Plasmid DNA: An Important
Assessing the Homogeneity of Plasmid DNA: An Important

... Figure 5. Agarose gel electrophoresis: two untreated plasmid samples and one sample of the plasmid transferred into the oc-form. ...
Des - Evolution of Developmental Genes
Des - Evolution of Developmental Genes

Horizontal Transfer of DNA From GM Crops to Bacteria and to
Horizontal Transfer of DNA From GM Crops to Bacteria and to

... or partially digested are not likely to be reformed if transformed into bacteria, and would therefore behave as any other randomly cleaved segment of DNA. One laboratory has reported studies of DNA survival in the animal intestine in which M13 phage or plasmid DNA fed to mice was detectable in feces ...
Structure of Nucleic Acids
Structure of Nucleic Acids

... DNA consists of two long polymers of simple units called nucleotides, with backbones made of sugarsand phosphate groups joined by ester bonds. These two strands run in opposite directions to each other and are therefore anti-parallel. Attached to each sugar is one of four types of molecules called b ...
Supplemental Appendix A: ClueGene Algorithm and Time
Supplemental Appendix A: ClueGene Algorithm and Time

... G; G has size g = |G|. Each dataset corresponds to an experiment series and consists of clusters of genes derived from experimental data. The number of datasets is d = |D|. There are two steps in the ClueGene scoring algorithm. First, dataset-specific scores are calculated for each gene. That is, ea ...
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Genomic library



A genomic library is a collection of the total genomic DNA from a single organism. The DNA is stored in a population of identical vectors, each containing a different insert of DNA. In order to construct a genomic library, the organism's DNA is extracted from cells and then digested with a restriction enzyme to cut the DNA into fragments of a specific size. The fragments are then inserted into the vector using DNA ligase. Next, the vector DNA can be taken up by a host organism - commonly a population of Escherichia coli or yeast - with each cell containing only one vector molecule. Using a host cell to carry the vector allows for easy amplification and retrieval of specific clones from the library for analysis.There are several kinds of vectors available with various insert capacities. Generally, libraries made from organisms with larger genomes require vectors featuring larger inserts, thereby fewer vector molecules are needed to make the library. Researchers can choose a vector also considering the ideal insert size to find a desired number of clones necessary for full genome coverage.Genomic libraries are commonly used for sequencing applications. They have played an important role in the whole genome sequencing of several organisms, including the human genome and several model organisms.
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