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Performance comparison of four exome capture systems for deep sequencing
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Tara Holley et al.
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Michal R. Schweiger et al.
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Michael J. Clark et al.
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A comparative analysis of exome capture
Jennifer S. Parla et al.
GENOME BIOLOGY (2011)
Comparison of solution-based exome capture methods for next generation sequencing
Anna-Maija Sulonen et al.
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Comprehensive comparison of three commercial human whole-exome capture platforms
Asan et al.
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Fast and accurate long-read alignment with Burrows-Wheeler transform
Heng Li et al.
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BEDTools: a flexible suite of utilities for comparing genomic features
Aaron R. Quinlan et al.
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The Sequence Alignment/Map format and SAMtools
Heng Li et al.
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Michal R. Schweiger et al.
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D. Talaulikar et al.
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The genomic landscapes of human breast and colorectal cancers
Laura D. Wood et al.
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A multiplex PCR predictor for aCGH success of FFPE samples
EH van Beers et al.
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R Sordella et al.
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EGFR mutations in lung cancer:: Correlation with clinical response to gefitinib therapy
JG Paez et al.
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Effect of fixatives and tissue processing on the content and integrity of nucleic acids
M Srinivasan et al.
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