PredWES ist ein Tool zur Berechnung der Wahrscheinlichkeit positiver Ergebnisse in Exomsequenzierungsstudien basierend auf klinischen Befunden. Es kann zur evidenzbasierten Entscheidungsfindung bei der Beantragung genetischer Studien genutzt werden.
Indikationen zur Durchführung einer NGS-Sequenzierung:
19955111
{19955111:MSAEZJH9}
1
Vancouver
50
Standard
150
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1.
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