Comprehensive comparison of three commercial human whole-exome capture platforms
暂无分享,去创建一个
Hui Jiang | Jun Wang | Jian Wang | Yali Xue | Chris Tyler-Smith | Asan | Huangming Yang | Xiao Liu | C. Tyler-Smith | Jian Wang | Jun Wang | G. Tian | Xiuqing Zhang | Hui Jiang | T. Jiang | Yali Xue | Mingzhi Wu | Jian Wang | Jun Wang | Huangming Yang | Yu Xu | Jiawei Wang | Xiao Liu | Geng Tian | Xiuqing Zhang | Tao Jiang | Yu Xu | Jiawei Wang | Mingzhi Wu | Jiawei Wang | Yu Xu
[1] Judy H. Cho,et al. Finding the missing heritability of complex diseases , 2009, Nature.
[2] Xin Jin,et al. TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing. , 2010, Brain : a journal of neurology.
[3] Emily H Turner,et al. Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome , 2010, Nature Genetics.
[4] Jay Shendure,et al. Methods for genomic partitioning. , 2009, Annual review of genomics and human genetics.
[5] Jamie K Teer,et al. Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing. , 2010, Genome research.
[6] J. Kitzman,et al. Whole exome capture in solution with 3 Gbp of data , 2010, Genome Biology.
[7] Tom Walsh,et al. Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82. , 2010, American journal of human genetics.
[8] Z. Xuan,et al. Genome-wide in situ exon capture for selective resequencing , 2007, Nature Genetics.
[9] Emily H Turner,et al. Target-enrichment strategies for next-generation sequencing , 2010, Nature Methods.
[10] International Human Genome Sequencing Consortium. Initial sequencing and analysis of the human genome , 2001, Nature.
[11] J. Maguire,et al. Solution Hybrid Selection with Ultra-long Oligonucleotides for Massively Parallel Targeted Sequencing , 2009, Nature Biotechnology.
[12] Nancy F. Hansen,et al. Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry , 2008, Nature.
[13] Huanming Yang,et al. SNP detection for massively parallel whole-genome resequencing. , 2009, Genome research.
[14] Emily H Turner,et al. Targeted Capture and Massively Parallel Sequencing of Twelve Human Exomes , 2009, Nature.
[15] Jonathan C. Cohen,et al. Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia. , 2010, The New England journal of medicine.
[16] Stylianos E. Antonarakis,et al. Mendelian disorders deserve more attention , 2006, Nature Reviews Genetics.
[17] N. Blin,et al. A general method for isolation of high molecular weight DNA from eukaryotes. , 1976, Nucleic acids research.
[18] Dawei Li,et al. The diploid genome sequence of an Asian individual , 2008, Nature.
[19] James R. Knight,et al. Genome sequencing in microfabricated high-density picolitre reactors , 2005, Nature.
[20] M. Daly,et al. Genetic Mapping in Human Disease , 2008, Science.
[21] Francisco M. De La Vega,et al. Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding. , 2009, Genome research.
[22] I. Tikhonova,et al. Genetic diagnosis by whole exome capture and massively parallel DNA sequencing , 2009, Proceedings of the National Academy of Sciences.
[23] Thomas Meitinger,et al. Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency , 2010, Nature Genetics.
[24] M. Stratton,et al. The cancer genome , 2009, Nature.
[25] D. Mccormick. Sequence the Human Genome , 1986, Bio/Technology.
[26] P. Shannon,et al. Exome sequencing identifies the cause of a Mendelian disorder , 2009, Nature Genetics.
[27] Richard Durbin,et al. A large genome center's improvements to the Illumina sequencing system , 2008, Nature Methods.
[28] Robert B. Hartlage,et al. This PDF file includes: Materials and Methods , 2009 .
[29] Stephan J Sanders,et al. Whole exome sequencing identifies recessive WDR62 mutations in severe brain malformations , 2010, Nature.
[30] Siu-Ming Yiu,et al. SOAP2: an improved ultrafast tool for short read alignment , 2009, Bioinform..