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Epigenetic Inactivation of Chalcone Synthase-A
Epigenetic Inactivation of Chalcone Synthase-A

... C002 plants were treated with 5-azacytidine (Fig. 3C) or trichostatin A (Fig. 3D). The frequencies of cytosine methylation at CpG/CpNpG/CpNpN sites were reduced to 62.9%/55.8%/15.5% and 44.1%/46.1%/13.0% by treatments with 5-azacytidine and trichostatin A, respectively. The CaMV 35S promoter contain ...
Supplementary Information
Supplementary Information

... workflow for acquisition, quality control, and processing of clinically-annotated biospecimens into DNA and RNA for TCGA. Tumor tissues (and case-matched source of germline DNA) are shipped and maintained at -196oC from the tissue source sites (TSSs). The BCR generates and reviews “top” and “bottom” ...
Chromosome - World of Teaching
Chromosome - World of Teaching

... Although DNA packaging is also a problem in bacteria, the mechanism by which prokaryotic DNA are packaged in the cell appears distinct from that eukaryotes and is not well understood. ...
An assessment of the risks associated with the
An assessment of the risks associated with the

... Development of genetically modified (GM) plants is contentious, in part because bacterial antibiotic resistance (AR) genes are used in their construction and often become part of the plant genome. This arouses concern that cultivation of GM plants might provide a reservoir of AR genes that could pow ...
meiosis - Citrus College
meiosis - Citrus College

Using CRISPR for genetic alteration_Joffrey Maine
Using CRISPR for genetic alteration_Joffrey Maine

Genomic data mining
Genomic data mining

... databases, with various data representations or formats, making it very difficult to use a single query tool to search more than a single data source. Data mining is vital to bioinformatics as it allows users to go beyond simple browsing of genome browsers, such as Ensembl [1,2] or the UCSC Genome B ...
Specific biomolecules serve various functions in the body.
Specific biomolecules serve various functions in the body.

... b. Ear size is a trait that shows incomplete dominance. c. Ear size is controlled by the environment. d. Ear size is not genetically controlled. ...
the lysis/lysogeny switch in phage \lambda
the lysis/lysogeny switch in phage \lambda

... with no cooperativity does not lead to the same switch-like behaviour. ...
Genetic testinG
Genetic testinG

... genetic nurse, etc.). The following subsections break down the elements of informed consent, but to learn even more about informed consent, the National Human Genome Research Institute’s “Elements of Informed Consent” (http://www. genome.gov/27526659) further explains the elements of this process. T ...
Pattern of diversity in the genomic region near the
Pattern of diversity in the genomic region near the

De Novo Sequencing and Homology Search with De Novo
De Novo Sequencing and Homology Search with De Novo

... – First, compute many (e.g. 10,000) sequences using an efficient score function that uses only a few of the most important ions. – Then, evaluate these candidates using a more sophisticated scoring function additional ions. ...
Annotation Practice Activity [Based on materials from the GEP
Annotation Practice Activity [Based on materials from the GEP

... The phase is the number of bases “left over” after the last full codon in the exon. Thus, to prevent a frame shift, the phases at the end of exon and the beginning of the next must add up to three. Sometimes there are multiple possible splice sites so you will need to determine the most likely corre ...
3- PARTE I Comparative cytogenetic mapping of Sox2 and
3- PARTE I Comparative cytogenetic mapping of Sox2 and

Supplemental File 1 - Poly(A) Tag (PAT) analysis pipeline The
Supplemental File 1 - Poly(A) Tag (PAT) analysis pipeline The

A genome screen for linkage in Australian sibling-pairs with
A genome screen for linkage in Australian sibling-pairs with

... distribution of the disease, systematic efforts to locate susceptibility genes have concentrated exclusively on populations from the Northern Hemisphere. We performed a genome wide screen of linkage in the Australian population using a panel of 397 microsatellite markers in 54 affected sibling-pairs ...
Handout - 6 - CM - Outline Genomic Model for HL7 V2
Handout - 6 - CM - Outline Genomic Model for HL7 V2

... This panel code does not carry values in its OBX-5 It defines the structure within the LOINC data base. It will not be included in the message since we are planning to use OBX-4 content to define the hierarchy rather than by nested OBRs The code for the CWE is the ID specified for the variant in the ...
Chapter 3: Molecular Biology Problems
Chapter 3: Molecular Biology Problems

... • The ball and stick view shows covalent bonds as rods and is most useful for determining which atoms are covalently bonded to each other. • The spacefill view shows atoms as joined spheres of their approximate actual size in the molecule. It is most useful for determining which atoms are closest to ...
mRNA Expression Analysis
mRNA Expression Analysis

... cDNA fragments to be sequenced. Supplied sequencing adaptors are ligated to the cDNA fragments, which are size-selected by gel electrophoresis and excision. A limited cycle PCR step ensures minimal contamination of RNA and unligated cDNA remains in the sample. These mRNA template libraries are seque ...
Diamond GM Risk Assessment Guidance
Diamond GM Risk Assessment Guidance

Aus dem  Max-Planck-Institut für Psychiatrie
Aus dem Max-Planck-Institut für Psychiatrie

... 1.1.1 Overview of Function All organisms strive towards maintaining their homeostasis, i.e. the dynamic equilibrium of their internal milieus that is essential for survival. The challenge of homeostasis by internal or external factors is classically referred to as “stress”. “Stress reaction” is the ...
nCounter® Data Analysis Guidelines for Copy Number
nCounter® Data Analysis Guidelines for Copy Number

... The Custom CNV Assay Kit comes with a set of four DNA controls that, when added to your genomic DNA sample prior to fragmentation, will monitor the efficiency of enzymatic digestion and heat denaturation. The DNA targets for probes labeled RESTRICTIONSITE+A and RESTRICTIONSITE+B contain an AluI rest ...
Cytogenetics
Cytogenetics

... Results from errors in division during meiosis, where a daughter cell receives both pairs of a particular chromosome (nondisjunction errors). Addition of an extra chromosome, trisomy, has been described for all the chromosomes but only three autosomal trisomies survive to birth. Those are trisomies ...
Compressed q-gram Indexing for Highly Repetitive Biological
Compressed q-gram Indexing for Highly Repetitive Biological

Contig annotation tool CAT robustly classifies assembled
Contig annotation tool CAT robustly classifies assembled

... questions in metagenomics (Handelsman, 2004)⁠ i.e. "Who is there?" and "What are they doing?". Read mapping considers each read as an independent observation, whose taxonomic origin and functional class can be estimated by identifying the closest match in a reference database, and tallying these ann ...
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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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