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WORKSHOP BOOK Fluorescent in Situ Hybridisation - FISH - on Human Sperm

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<str<strong>on</strong>g>FISH</str<strong>on</strong>g> Advantages<br />

) Less labor-<str<strong>on</strong>g>in</str<strong>on</strong>g>tensive method<br />

2) Used at uncultured cells<br />

3) Own c<strong>on</strong>trol<br />

4) No diluti<strong>on</strong> factor<br />

5) Small sample size<br />

6) Multiple target analysis<br />

7) Rather quick (possibly next day result)<br />

8)Easy to perform<br />

33<br />

<str<strong>on</strong>g>FISH</str<strong>on</strong>g> Disadvantages<br />

Can detect “known” or “suspected” abnormalities<br />

Not screen<str<strong>on</strong>g>in</str<strong>on</strong>g>g of chromosomal rearrangement<br />

No structural abnormalities<br />

No differentiati<strong>on</strong> between nullisomy & hybridisati<strong>on</strong><br />

failures<br />

Only 1-3 probe-signal / sperm head<br />

Cost<br />

Needs experienced technician<br />

Scor<str<strong>on</strong>g>in</str<strong>on</strong>g>g – Time c<strong>on</strong>sum<str<strong>on</strong>g>in</str<strong>on</strong>g>g<br />

(low aneuploidy rate/chromosome affected by sample's<br />

size)<br />

Automated <strong>Sperm</strong>-<str<strong>on</strong>g>FISH</str<strong>on</strong>g>?<br />

34

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