Strand NGS Variant Caller A Benchmarking Study
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چکیده
منابع مشابه
Systematic comparison of variant calling pipelines using gold standard personal exome variants
The success of clinical genomics using next generation sequencing (NGS) requires the accurate and consistent identification of personal genome variants. Assorted variant calling methods have been developed, which show low concordance between their calls. Hence, a systematic comparison of the variant callers could give important guidance to NGS-based clinical genomics. Recently, a set of high-co...
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Motivation: The usual approach to variant calling from NGS data consists in inferring single nucleotide variants (SNVs) or more complex differences from read alignments. Consequently, variant calling is performed after all reads have been mapped to a reference genome and all read alignments are available. Existing variant callers usually operate by first sorting the alignments in increasing ord...
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تاریخ انتشار 2015