Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications

Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications

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High-throughput DNA sequencing technology has transformed genetic research and is starting to make an impact on clinical practice. However, analyzing high-throughput sequencing data remains challenging, particularly in clinical settings where accuracy and turnaround times are critical. We present a...

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Xehetasun bibliografikoak
Egile Nagusiak:	Rimmer, A, Phan, H, Mathieson, I, Iqbal, Z, Twigg, S, Wilkie, A, Mcvean, G, Lunter, G
Formatua:	Journal article
Hizkuntza:	English
Argitaratua:	Nature Publishing Group 2014

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