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超低入力ヒトゲノム単一 Tardigrade の標本からのライブラリの準備
 

超低入力ヒトゲノム単一 Tardigrade の標本からのライブラリの準備

Article doi: 10.3791/57615
July 15th, 2018

Summary July 15th, 2018

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顕微鏡の有機体のゲノムのシーケンス処理中に汚染大きい問題に残る。ここでは、汚染のリスクを最小限に抑えるため全ゲノム増幅 DNA のわずか 50 pg を単一の標本からクマムシのゲノムをシーケンス処理する方法を示します。

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