An online copy number variant detectionmethod for short sequencing reads
Yazarlar (4)
Ayten Yiğiter Hacettepe Üniversitesi, Türkiye
Jie Chen Augusta University, Amerika Birleşik Devletleri
Lingling An Department Of Biosystems Engineering, Amerika Birleşik Devletleri
Dr. Öğr. Üyesi Nazan DANACIOĞLU Sinop Üniversitesi, Türkiye
Makale Türü Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale)
Dergi Adı Journal of Applied Statistics (Q4)
Dergi ISSN 0266-4763 Dergi Bilgileri (2015)
Dergi Tarandığı Indeksler SSCI
Makale Dili İngilizce Basım Tarihi 07-2015
Kabul Tarihi Yayınlanma Tarihi 28-01-2015
Cilt / Sayı / Sayfa 42 / 7 / 1556–1571 DOI 10.1080/02664763.2014.1001330
Makale Linki http://www.tandfonline.com/doi/full/10.1080/02664763.2014.1001330
UAK Araştırma Alanları
İstatistiksel Deney Tasarımı
Özet
The availability of the next generation sequencing (NGS) technology in today's biomedical research has provided new opportunities in scientific discovery of genetic information. The high-throughput NGS technology, especially DNA-seq, is particularly useful in profiling a genome for the analysis of DNA copy number variants (CNVs). The read count (RC) data resulting from NGS technology are massive and information rich. How to exploit the RC data for accurate CNV detection has become a computational and statistical challenge. We provide a statistical online change point method to help detect CNVs in the sequencing RC data in this paper. This method uses the idea of online searching for change point (or breakpoint) with a Markov chain assumption on the breakpoints loci and an iterative computing process via a Bayesian framework. We illustrate that an online change-point detection method is particularly …
Anahtar Kelimeler
Bayesian estimate | change point (or breakpoint) | DNA copy number variation | next generation sequencing | online change-point detection method
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
Web of Science 6
Scopus 5
Google Scholar 7
An online copy number variant detectionmethod for short sequencing reads

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