An Integrated Approach for Analyzing Clinical Genomic Variant Data from Next-Generation Sequencing-Reference-Cited by-同舟云学术

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An Integrated Approach for Analyzing Clinical Genomic Variant Data from Next-Generation Sequencing

Published:2015-04 Issue:1 Volume:26 Page:19-28
ISSN:1524-0215
Container-title:Journal of Biomolecular Techniques : JBT
language:
Short-container-title:J Biomol Tech

Author:

Crowgey Erin L.,Stabley Deborah L.,Chen Chuming,Huang Hongzhan,Robbins Katherine M.,Polson Shawn W.,Sol-Church Katia,Wu Cathy H.

Publisher

Association of Biomolecular Resource Facilities

Subject

Molecular Biology

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. PEcnv: accurate and efficient detection of copy number variations of various lengths;Briefings in Bioinformatics;2022-09

2. The Tumor Dynamism Is the Dark Matter of the NGS Galaxy: How to Understand It?;Cancers;2021-10-30

3. Development and validation of Houston Methodist Variant Viewer version 3: updates to our application for interpretation of next-generation sequencing data;JAMIA Open;2020-03-17

4. Clinical Utility of Next-generation Sequencing in the Management of Myeloproliferative Neoplasms: A Single-Center Experience;HemaSphere;2018-06

5. Detection of copy number variations by pair analysis using next-generation sequencing data in inherited kidney diseases;Clinical and Experimental Nephrology;2018-01-25

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