ERDS-pe: A paired hidden Markov model for copy number variant detection from whole-exome sequencing data
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Yadong Wang | Rui Ma | Rongjie Wang | Shuilin Jin | Xiaoliang Wu | Zhijie Han | Qinghua Jiang | Guoqiang Wan | Wenyang Zhou | Renjie Tan | Jixuan Wang | Yadong Wang | Qinghua Jiang | Shuilin Jin | Zhijie Han | Wenyang Zhou | Rui Ma | Jixuan Wang | Xiaoliang Wu | Renjie Tan | Rongjie Wang | Guoqiang Wan
[1] D. Goldstein,et al. Uncovering the roles of rare variants in common disease through whole-genome sequencing , 2010, Nature Reviews Genetics.
[2] J. Potash,et al. Validation and assessment of variant calling pipelines for next-generation sequencing , 2014, Human Genomics.
[3] B. Williams,et al. Mapping and quantifying mammalian transcriptomes by RNA-Seq , 2008, Nature Methods.
[4] Yufeng Shen,et al. CANOES: detecting rare copy number variants from whole exome sequencing data , 2014, Nucleic acids research.
[5] M. Hurles,et al. Copy number variation in human health, disease, and evolution. , 2009, Annual review of genomics and human genetics.
[6] Nancy R. Zhang,et al. CODEX: a normalization and copy number variation detection method for whole exome sequencing , 2015, Nucleic acids research.
[7] E. Banks,et al. Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth. , 2012, American journal of human genetics.
[8] Kenny Q. Ye,et al. Large-Scale Copy Number Polymorphism in the Human Genome , 2004, Science.
[9] Agus Salim,et al. Statistical challenges associated with detecting copy number variations with next-generation sequencing , 2012, Bioinform..
[10] Bradley P. Coe,et al. Copy number variation detection and genotyping from exome sequence data , 2012, Genome research.
[11] Xiaolin Zhu,et al. An Evaluation of Copy Number Variation Detection Tools from Whole‐Exome Sequencing Data , 2014, Human mutation.
[12] Kenny Q. Ye,et al. Mapping copy number variation by population scale genome sequencing , 2010, Nature.
[13] Tomas W. Fitzgerald,et al. Origins and functional impact of copy number variation in the human genome , 2010, Nature.
[14] Wilko Spiering,et al. Diagnostic Clinical Genome and Exome Sequencing , 2014 .
[15] Celine S. Hong,et al. Assessing the reproducibility of exome copy number variations predictions , 2016, Genome Medicine.
[16] Deborah A Nickerson,et al. De novo rates and selection of large copy number variation. , 2010, Genome research.
[17] Clara Gaff,et al. Patient safety in genomic medicine: an exploratory study , 2016, Genetics in Medicine.