Kevlar: A Mapping-Free Framework for Accurate Discovery of De Novo Variants
Summary: De novo genetic variants are an important source of causative variation in complex genetic disorders. Many methods for variant discovery rely on mapping reads to a reference genome, detecting numerous inherited variants irrelevant to the phenotype of interest. To distinguish between inherit...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2019-08-01
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Series: | iScience |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2589004219302597 |