affy2sv: an R package to pre-process Affymetrix CytoScan HD and 750K arrays for SNP, CNV, inversion and mosaicism calling-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

affy2sv: an R package to pre-process Affymetrix CytoScan HD and 750K arrays for SNP, CNV, inversion and mosaicism calling

Published:2015-05-20 Issue:1 Volume:16 Page:
ISSN:1471-2105
Container-title:BMC Bioinformatics
language:en
Short-container-title:BMC Bioinformatics

Author:

Hernandez-Ferrer Carles,Quintela Garcia Ines,Danielski Katharina,Carracedo Ángel,Pérez-Jurado Luis A.,González Juan R.

Publisher

Springer Science and Business Media LLC

Subject

Applied Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Structural Biology

Link

http://link.springer.com/article/10.1186/s12859-015-0608-y/fulltext.html

Reference49 articles.

1. Chih-yu Chen, I-Shou C, Chao AH and Wyeth WW On the identification of potential regulatory variants within genome wide association candidate SNP sets. BMC Medical Genomics. 2014; doi:10.1186/1755-8794-7-34.

2. Barrdahl M, Canzian F, Joshi AD, Travis RC, Chang-Claude J, Auer PL, et al. Post-GWAS gene-environment interplay in breast cancer: results from the Breast and Prostate Cancer Cohort Consortium and a meta-analysis on 79 000 women. Hum Mol Genet. 2014. doi:10.1093/hmg/ddu223.

3. Na L , Ping Z, Jian Z, Jieqiong D, Hongchun W, Wei L, et al. A Polymorphism rs12325489C>T in the LincRNA-ENST00000515084 Exon Was Found to Modulate Breast Cancer Risk via GWAS-Based Association Analyses. PLoS One. 2014. doi:10.1371/journal.pone.0098251.

4. Johnson ME, Schug J, Wells AD, Kaestner KH, Grant SF. Genome-Wide Analyses of ChIP-Seq Derived FOXA2 DNA Occupancy in Liver Points to Genetic Networks Underpinning Multiple Complex Traits. J Clin Endocrinol Metab. 2014. doi:10.1210/jc.2013-4503.

5. Melén E, Granell R, Kogevinas M, Strachan D, Gonzalez JR, Wjst M, et al. Genome-wide association study of body mass index in 23 000 individuals with and without asthma. Clin Exp Allergy. 2013. doi:10.1111/cea.12054.

Cited by 4 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. Fully exploiting SNP arrays: a systematic review on the tools to extract underlying genomic structure;Briefings in Bioinformatics;2022-02-24

2. Cyclin E Overexpression in Human Mammary Epithelial Cells Promotes Epithelial Cancer-Specific Copy Number Alterations;iScience;2019-09

3. Metabolic characterization of isocitrate dehydrogenase (IDH) mutant and IDH wildtype gliomaspheres uncovers cell type-specific vulnerabilities;Cancer & Metabolism;2018-04-17

4. Genome-wide analysis of somatic copy number alterations and chromosomal breakages in osteosarcoma;International Journal of Cancer;2017-05-25

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3