RareVar: A Framework for Detecting Low-Frequency Single-Nucleotide Variants-Reference-Cited by-同舟云学术

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RareVar: A Framework for Detecting Low-Frequency Single-Nucleotide Variants

Published:2017-07 Issue:7 Volume:24 Page:637-646
ISSN:1557-8666
Container-title:Journal of Computational Biology
language:en
Short-container-title:Journal of Computational Biology

Author:

Hao Yangyang¹²,Xuei Xiaoling³⁴,Li Lang¹²,Nakshatri Harikrishna⁵⁶,Edenberg Howard J.¹³⁴,Liu Yunlong¹²⁴⁶

Affiliation:

1. Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana.

2. Center for Computational Biology and Bioinformatics, Indiana University School of Medicine, Indianapolis, Indiana.

3. Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana.

4. Center for Medical Genomics, Indiana University School of Medicine, Indianapolis, Indiana.

5. Department of Surgery, Indiana University School of Medicine, Indianapolis, Indiana.

6. IU Simon Cancer Center, Indiana University School of Medicine, Indianapolis, Indiana.

Publisher

Mary Ann Liebert Inc

Subject

Computational Theory and Mathematics,Computational Mathematics,Genetics,Molecular Biology,Modeling and Simulation

Link

http://www.liebertpub.com/doi/pdf/10.1089/cmb.2017.0057

Reference23 articles.

1. An integrated map of genetic variation from 1,092 human genomes

2. Absolute quantification of somatic DNA alterations in human cancer

Cited by 5 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. Identification of Somatic Mutations From Bulk and Single-Cell Sequencing Data;Frontiers in Aging;2022-01-03

2. Influence of sequencing depth on the fidelity and sensitivity of 1%-5% low-frequency mutation detection and recommendation for standardization of sequencing depth;2021-12-27

3. Translating cancer genomics into precision medicine with artificial intelligence: applications, challenges and future perspectives;Human Genetics;2019-01-22

4. What Does This Mutation Mean? The Tools and Pitfalls of Variant Interpretation in Lymphoid Malignancies;International Journal of Molecular Sciences;2018-04-20

5. A system for detecting high impact-low frequency mutations in primary tumors and metastases;Oncogene;2017-09-11

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