Improving bioinformatic pipelines for exome variant calling
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics,Molecular Biology,Molecular Medicine
Reference8 articles.
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5. The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
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1. Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-Küster-Hauser syndrome;Human Genetics and Genomics Advances;2023-07
2. Detecting sequence variants in clinically important protozoan parasites;International Journal for Parasitology;2020-01
3. Bioinformatics Pipelines for Targeted Resequencing and Whole-Exome Sequencing of Human and Mouse Genomes: A Virtual Appliance Approach for Instant Deployment;PLoS ONE;2014-04-21
4. Variant Callers for Next-Generation Sequencing Data: A Comparison Study;PLoS ONE;2013-09-27
5. Computational and Bioinformatics Frameworks for Next-Generation Whole Exome and Genome Sequencing;The Scientific World Journal;2013
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