A reference human genome dataset of the BGISEQ-500 sequencer
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Hui Jiang | Wenwei Zhang | Xinming Liang | Shoufang Qu | Junhua Rao | Sha Liao | Shangxian Gao | Zhaopeng Yang | Jiahao Wang | Chunyu Geng | Feng Mu | Jie Huang | Wenwei Zhang | Hui Jiang | Yuxiang Li | Junhua Rao | Haorong Lu | F. Mu | Xinming Liang | Jiahao Wang | C. Geng | Haorong Lu | Jie Huang | Zhaopeng Yang | Yuxiang Li | Ting Yu | Yuankai Xuan | Xianglin Mei | Hongbo Chen | Nan Sun | Ying Chen | Xin Liu | Shangxian Gao | Sha Liao | Ting Yu | Xin Liu | Nan Sun | Ying Chen | Shoufang Qu | Yuankai Xuan | Xianglin Mei | Hongbo Chen | C. Geng
[1] J. Zook,et al. Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls , 2013, Nature Biotechnology.
[2] Mauricio O. Carneiro,et al. From FastQ Data to High‐Confidence Variant Calls: The Genome Analysis Toolkit Best Practices Pipeline , 2013, Current protocols in bioinformatics.
[3] Richard Durbin,et al. Sequence analysis Fast and accurate short read alignment with Burrows – Wheeler transform , 2009 .
[4] E. Mardis. Next-generation sequencing platforms. , 2013, Annual review of analytical chemistry.
[5] Robert B. Hartlage,et al. This PDF file includes: Materials and Methods , 2009 .
[6] Alexa B. R. McIntyre,et al. Extensive sequencing of seven human genomes to characterize benchmark reference materials , 2015, Scientific Data.
[7] J. McPherson,et al. Coming of age: ten years of next-generation sequencing technologies , 2016, Nature Reviews Genetics.
[8] Dawei Li,et al. The diploid genome sequence of an Asian individual , 2008, Nature.
[9] N. Lennon,et al. Characterizing and measuring bias in sequence data , 2013, Genome Biology.
[10] J. Long,et al. Steps to ensure accuracy in genotype and SNP calling from Illumina sequencing data , 2012, BMC Genomics.
[11] H. Swerdlow,et al. A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers , 2012, BMC Genomics.
[12] M. DePristo,et al. A framework for variation discovery and genotyping using next-generation DNA sequencing data , 2011, Nature Genetics.
[13] M. DePristo,et al. The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. , 2010, Genome research.
[14] Insuk Lee,et al. Systematic comparison of variant calling pipelines using gold standard personal exome variants , 2015, Scientific Reports.
[15] M. Metzker. Sequencing technologies — the next generation , 2010, Nature Reviews Genetics.