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14.8K Views
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14:06 min
June 23rd, 2012
DOI :
10.3791/3943-v
Chapters
0:05
Title
1:28
Pooled PCR Library Preparation and Sequencing
4:46
Sequencing Reads Alignment and Analysis
7:35
Rare Variant Detection using SPLINTER
11:11
SPLINTER Results: Detection of Rare Genomic Variants from Pooled Sequencing
13:24
Conclusion
Summary
汇集DNA测序检测与大同伙的复杂表型相关的罕见的变异是一个快速和具有成本效益的战略。在这里,我们描述的汇集,32个癌症相关的基因,利用分裂软件包下一代测序的计算分析。这种方法可扩展性,适用于任何利益型。
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