Discovery of common sequences absent in the human reference genome using pooled samples from next generation sequencing

被引：0
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作者：
Yu Liu
Mehmet Koyutürk
Sean Maxwell
Min Xiang
Martina Veigl
Richard S Cooper
Bamidele O Tayo
Li Li
Thomas LaFramboise
Zhenghe Wang
Xiaofeng Zhu
Mark R Chance
机构：
[1] Case Western Reserve University,Center for Proteomics and Bioinformatics
[2] Case Western Reserve University,Department of Electrical Engineering & Computer Science
[3] Case Western Reserve University,Case Comprehensive Cancer Center
[4] Case Western Reserve University,Department of Genetics and Genome Science
[5] Case Western Reserve University,Department of Family Medicine and Community Health
[6] Case Western Reserve University,Department of General Medical Sciences
[7] Case Western Reserve University,Department of Epidemiology and Biostatistics
[8] Suzhou Health College,Department of Pharmacy
[9] Loyola University Chicago,Department of Public Health Sciences, Stritch School of Medicine
来源：
BMC Genomics | / 15卷
关键词：
Missing common sequence; De novo assembling; Next generation sequencing; Expression in brain; Transcription factor binding; Genome evolution;
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