Quantifying single nucleotide variant detection sensitivity in exome sequencing

Title
Quantifying single nucleotide variant detection sensitivity in exome sequencing
Authors
Keywords
Read Depth, Single Nucleotide Variant, Reference Allele, Capture Method, Full Alignment
Journal
BMC BIOINFORMATICS
Volume 14, Issue 1, Pages 195
Publisher
Springer Nature
Online
2013-06-18
DOI
10.1186/1471-2105-14-195

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