22. Genomics I: Analysis of DNA Flashcards

1
Q

all of the chromosomes and DNA sequences that an organism or species can possess.

A

Genome

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2
Q

the molecular analysis of the entire genome of a species.

A

Genomics

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3
Q

the study of gene function at the genome level. It involves the study of many genes simultaneously.

A

Functional Genomics

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4
Q

the study of protein function at the genome level. It involves the study of many proteins simultaneously.

A

Proteomics

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5
Q

the experimental process of determining the relative locations of genes or other segments of DNA on individual chromosomes.

A

Mapping

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6
Q

determining the locations of specific genetic sequences within chromosomes using microscopy. Also called cytological mapping.

A

Cytogenetic Mapping

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7
Q

determining the relative spacing and order of genes along a chromosome by analyzing the outcomes of crosses.

A

Linkage Mapping

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8
Q

determining the locations of and distances between genes and other genetic sequences on a chromosome using DNA-cloning and/or DNA sequencing techniques.

A

Physical Mapping

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9
Q

a diagram that shows the relative locations of genes or other DNA segments on a chromosome.

A

Genetic (Chromosome) Map

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10
Q

the physical location of a gene or other DNA segment within a chromosome.

A

Locus (Loci)

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11
Q

a technique used to cytologically map the locations of genes or other DNA sequences within large eukaryotic chromosomes. In this method, a complementary probe is used to detect the location of a gene within a set of chromosomes.

A

In Situ Hybridization

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12
Q

the phenomenon in which two single-stranded DNA molecules from different sources bind to form a hybrid molecule.

A

Hybridization

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13
Q

a form of in situ hybridization in which the DNA probe is fluorescently labeled.

A

Fluorescence In Situ Hybridization (FISH)

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14
Q

the use of fluorescently labeled probes to identify multiple sites along one or more chromosomes. The probes are usually assigned different computer-generated colors.

A

Chromosome Painting

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15
Q

a segment of DNA that is found at a specific site along a chromosome and has properties that enable it to be uniquely recognized using molecular tools, such as PCR and gel electrophoresis.

A

Molecular Marker

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16
Q

a term used to describe a trait or gene (or other segment of DNA) that is found in two or more forms in a population.

A

Polymorphic

17
Q

a molecular marker composed of many repeated copies of a short sequence. Microsatellites are interspersed throughout a genome and are quite variable in length among different individuals. They can be amplified by PCR.

A

Microsatellites

18
Q

a short segment of DNA, whose base sequence is found to be unique within an entire genome. Sequence-tagged sites are identified by PCR.

A

Sequence-Tagged Site (STS)

19
Q

with regard to genetic diseases, an individual who lived many generations ago and was the person in which the disease-causing allele originated.

A

Founder

20
Q

a series of clones that contain contiguous, overlapping pieces of chromosomal DNA.

A

Contig

21
Q

cloning vectors that can accommodate large DNA inserts and behave like chromosomes when inside of living cells.

A

Artificial Chromosomes

22
Q

a cloning vector propagated in yeast that can reliably contain very large inserted fragments of DNA.

A

yeast artificial chromosome (YAC)

23
Q

a type of cloning vector that propagates in bacteria and is used to clone large fragments of DNA.

A

bacterial artificial chromosome (BAC)

24
Q

a type of cloning vector developed from P1 bacteriophage DNA that can carry an insert with a length of 300,000 bp or more.

A

P1 artificial chromosome (PAC)

25
Q

a cloning strategy in which a gene is cloned based on its mapped position on a chromosome.

A

positional cloning

26
Q

a method used in positional cloning in which a mapped gene or molecular marker provides a starting point from which to molecularly “walk” toward a gene of interest via overlapping clones.

A

chromosome walking

27
Q

the procedure of making smaller DNA clones from a larger one.

A

subcloning

28
Q

research endeavors that have the ultimate goal of determining the sequence of DNA bases of the entire genome of a given species.

A

genome-sequencing projects

29
Q

a genome-sequencing approach in which DNA fragments to be sequenced are randomly generated from larger DNA fragments.

A

shotgun sequencing

30
Q

a worldwide collaborative project that provided a detailed map of the human genome and obtained its complete DNA sequence.

A

Human Genome Project

31
Q

the ability to sequence large amounts of DNA in a short period of time. It usually involves the sequencing of many samples at the same time.

A

high-throughput sequencing

32
Q

newer DNA-sequencing technologies that are more rapid and inexpensive than the dideoxy method.

A

next-generation sequencing technologies

33
Q

a type of next-generation DNA-sequencing technology.

A

pyrosequencing

34
Q

a next-generation DNA-sequencing method in which the synthesis of DNA is directly monitored to deduce the base sequence.

A

sequencing by synthesis (SBS)

35
Q

using information from genome-sequencing projects to understand the genetic variation between different populations and evolutionary relationships among different species.

A

comparative genomics

36
Q

the study of a complex mixture of genetic material obtained from an environmental sample.

A

metagenomics

37
Q

a collection of genes from an environmental sample.

A

metagenome

38
Q
A