Ch. 20 Flashcards

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1
Q

ChiP steps

A

1- Proteins are fixed to DNA, 2- shear DNA into fragments, 3- immunoprecipitation with antibodies, 4- protein and antibody release from chromatin (reverse crosslink), 5- sequence is recovered from a pool of associated DNA

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2
Q

Contig assembly

A

overlap of restriction enzyme digest pattern- DNA marker or other known sequence can be used to determine clone order to assemble a contig

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3
Q

What are the two approaches to whole genomic sequencing?

A

map based approach and whole genome shotgun sequencing

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4
Q

describe the map based approach for whole genomic sequencing

A

it uses detailed genetic and physical maps to identify the least number of clones to cover the genome, and then sequences and assembles the smaller number of clones

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5
Q

describe the whole genome shotgun sequencing

A

shear genome itno small pieces and clone; sequence millions of clones; and then assemble all those sequences

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6
Q

Human genome first drafted in

A

2000

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7
Q

Describe eukaryotic genomes

A

they are very repetitive

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8
Q

Roughly 2% of the human genome is _________

A

protein coding

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9
Q

Most genomic variation is in

A

single nucleotide polymorphisms

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9
Q

the genome wide association study uses…

A

pedigrees and linkage using SNP haplotypes to identify disease loci

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10
Q

What are single nucleotide polymorphisms

A

a site in the genome where individual members of a species differ in a single base pair

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11
Q

haplotypes

A

a specific set of linked genetic varients or alleles on a single chromosome

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12
Q

Manhattan plot

A

showing genomic regions associated with a trait

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13
Q

Synteny

A

colinearity between related genomes; the genomes are descended from a common ancestor

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14
Q

transgenic organisms

A

a way to analyze gene function; add DNA sequences of interest to the genome of an organism that normally lacks such sequences and then we can observe the effect of the introduced sequence on the organism’s phenotype

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15
Q

CRISPR-Cas9

A

can be used to target specific locations in the genome to introduce changes

16
Q

DNA fingerprinting

A

we can use variations in the genome to identify a person; short tandem repeats or microsatellites are known places of variation (people vary in the number of copies of repeats that they possess at each of these loci)

17
Q

Combined DNA index system

A

FBI system of STR loci to identify people and solve crimes