Part E: Lecture 36 Flashcards

1
Q

Timeline for DNA sequencing

A

Manual Sanger (1970s)
Automated Sanger (1980s)
Next Gen (2008)

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2
Q

Automated Sanger machine

A

ABI 3730

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3
Q

Next Gen machine

A

Illumina MiSeq
Illumina NextSeq 500

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4
Q

Automated Sanger Results

A

fluorescent coloured peaks for nucleotides (chromatogram)

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5
Q

Next Gen Results

A

list of letters corresponding to nucleotides (no chromatogram)

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6
Q

M. Sanger _____ by A. Sanger and now it is used with _____

A

replaced
Next Gen

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7
Q

dideoxynucleotides (ddNTPs) description

A

no 3’ OH

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8
Q

ddNTPs function

A

stop DNA replication

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9
Q

Cy3 emits ___ light

A

greenish-yellow

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10
Q

Cy5 emits ___ light

A

red

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11
Q

ddNTPs is connected to ____ to indicates ____

A

fluorescent dyes
nucleotide at specific position

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12
Q

DNA sequencing reaction mixture

A

Template DNA
one oligo primer
Taq DNA Pol
lots of normal dNTPs
some labeled ddNTPs

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13
Q

DNA sequencing steps

A

1) rxn mixture
2) in vitro DNA synthesis
3) Capillary electrophoresis

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14
Q

Machine for DNA sequencing

A

standard PCR machine

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15
Q

number of cycles of denature/anneal/extend for DNA sequencing

A

25 cycles

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16
Q

capillary electrophoresis

A

(-) electrode and (+) electrode connected via capillary tube which separates dna fragments according to size (smallest is first), laser fluoresces DNA and detector detects colour

17
Q

DNA sequencing results

A

Chromatogram

18
Q

useful data (range) for DNA sequencing

A

700 nt

19
Q

PCR vs. A. Sanger: product shape

A

PCR: dsDNA of equal length
A. Sanger: ssDNAs of unequal length

20
Q

PCR vs. A. Sanger: product number

A

PCR: 1 billion products per template
A. Sanger: 25 products per template

21
Q

PCR vs. A. Sanger: product max size

A

PCR: 5kb
A. Sanger: 700 nt

22
Q

A. Sanger sequencing is used for _____

A

sequencing plasmids and genes

23
Q

To make primers, we need to know ______

A

the sequence

24
Q

sequencing a plasmid steps

A

1)isolate plasmid DNA
2)sequence with primer

25
Q

sequencing a gene steps

A

1)isolate genomic DNA
2)PCR to amplify gene
3)sequencing with primer

26
Q

PCR vs. A. Sanger: # primers

A

PCR: 2 primers
A. Sanger: 1 primer

27
Q

DNA sequencing chromatogram: heterozygous

A

lower double peak