Methods for phasing and imputation of very low coverage sequencing data

Methods for phasing and imputation of very low coverage sequencing data

<p>The introduction of massively parallel short-read sequencing has facilitated rapidly dropping costs of DNA sequencing. This has led to substantial growth in the size of human sequencing projects, with consortia of low coverage sequencing data containing tens of thousands of samples. However...

Disgrifiad llawn

Manylion Llyfryddiaeth
Prif Awdur:	Kretzschmar, WW
Awduron Eraill:	Marchini, J
Fformat:	Traethawd Ymchwil
Iaith:	English
Cyhoeddwyd:	2016
Pynciau:	Statistical genetics Statistical methods Genomics

Eitemau Tebyg

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