Next generation sequencing Flashcards

1
Q

Explain the steps in NGS

A

flow cell channels

PCR

bridge amplication

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2
Q

What are the 2 types of end sequences? Explain.

A

Single end sequence
reads from one end of a fragment - reps, polymorphs, missing data - limit

paired end sequence
-more efficient - help link contigs into scaffolds

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3
Q

What type of software read the raw DNA data? What’s its format?

A

base-calling(phred)

FASTQ

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4
Q

What is genome assembly? 2 strategies used?

A

ss

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5
Q

explain de-novo sequence assembly? graphs created?

A

de brujin

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6
Q

reads, contigs, scaffolds?

A

ss

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7
Q

What features are in a genome annotation?

A

genes

repetitive

gc content & other nu compositions

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8
Q

Explain the approaches to finding protein-coding genes in genomic dna?

A

extrinsic - homology-based & reference based

intrinsic-algorithmic
features analyzed?

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9
Q

Gene prediction programs?

A

fgenesh, genscan

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10
Q

what is GBrowse?

A

ss

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