L-22 Flashcards

1
Q

When did the human genome project begin?

A

1990

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2
Q

What was the aim of the human genome project?

A
  • identify all human genes and their roles
  • analyse genetic variation between humans
  • sequence the genomes of many model organisms used in genetics
  • develop new sequencing techniques and computational analysis
  • to share genome information with scientists and the general public as fast as possible
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3
Q

What are the key findings of the human genomes:

A
  • there are fewer genes than expected
  • less than 2% of our genome codes for proteins
  • the genome is dynamic
  • we still don’t know what many of our protein coding genes do
  • most human genes are related to those of other animals
  • all humans are 99.9% similar at the sequence level
  • less than 2% of genetic material is exons
  • 20% of genetic material is introns
  • we have approximately 20000 genes
  • 20% of genes have unknown functions
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4
Q

What does SNP stand for

A

Single nucleotide polymorphisms

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5
Q

What are SNPs?

A

Sites in the DNA that commonly vary within populations

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6
Q

How many SNPs are in the genome?

A

1.9 million

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7
Q

What proportion of nucleotides are SNPs

A

1/300

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8
Q

Where determines the SNP’s of an individual?

A

Their parent’s

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9
Q

What do SNPs do?

A

Usually nothing but can be used for sequencing genome things

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10
Q

What can analysing common variants of SNPs do?

A
  • who you are related to
  • where your ansestors came from
  • risk of disease
  • muscle type
  • how you might respond to drugs
  • can be used in crime solving
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11
Q

What does STR stand for?

A

Short tandem repeats

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12
Q

What are STRs?

A

Repeats of 2-5 nucleotides found in specific regions of the genome

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13
Q

Can homologous chromosomes have different lengths of STRs?

A

Yes because each person inherits one allele from each parent

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14
Q

What can STR (lengths) be used for?

A
  • create genetic profiles

- “DNA fingerprints” specific to each person

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15
Q

What are InDels?

A

Small insertions or deletions in the genome

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16
Q

What are CNVs?

A

Chunks of DNA composed of more than 500 base pairs that are present in different amount s or “copy numbers” relative to a reference genome

17
Q

What does CNV stand for?

A

Copy number variations

18
Q

How many CNVs are found within and between genes in the human genome?

A

10, 000

19
Q

What are many genes found in CNVs associated with?

A

Sensory perception and immunity

20
Q

What are extra copies of the AMY1 gene associated with?

A

Better starch digestion