Atlas2 Cloud: a framework for personal genome analysis in the cloud
暂无分享,去创建一个
Aleksandar Milosavljevic | Cristian Coarfa | Fuli Yu | Uday S. Evani | Danny Challis | Jin Yu | Andrew R. Jackson | Sameer Paithankar | A. Milosavljevic | F. Yu | M. Bainbridge | C. Coarfa | Peter Pham | Danny Challis | Jin Yu | Sameer Paithankar | Andrew R Jackson | Matthew N Bainbridge | Uday S Evani | Adinarayana Jakkamsetti | Peter Pham | Adinarayana Jakkamsetti
[1] David R. Murdock,et al. Whole-Genome Sequencing for Optimized Patient Management , 2011, Science Translational Medicine.
[2] Daniel J. Blankenberg,et al. Galaxy: A Web‐Based Genome Analysis Tool for Experimentalists , 2010, Current protocols in molecular biology.
[3] Emily H Turner,et al. Targeted Capture and Massively Parallel Sequencing of Twelve Human Exomes , 2009, Nature.
[4] M. DePristo,et al. The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. , 2010, Genome research.
[5] David Haussler,et al. The UCSC genome browser database: update 2007 , 2006, Nucleic Acids Res..
[6] Aleksandar Milosavljevic,et al. Enabling Atlas2 personal genome analysis on the cloud , 2011, 2011 IEEE International Workshop on Genomic Signal Processing and Statistics (GENSIPS).
[7] Mary Goldman,et al. The UCSC Genome Browser database: update 2011 , 2010, Nucleic Acids Res..
[8] Michael C. Schatz,et al. CloudBurst: highly sensitive read mapping with MapReduce , 2009, Bioinform..
[9] Alexander A. Morgan,et al. Clinical assessment incorporating a personal genome , 2010, The Lancet.
[10] M. Schatz,et al. Searching for SNPs with cloud computing , 2009, Genome Biology.
[11] Gonçalo R. Abecasis,et al. The Sequence Alignment/Map format and SAMtools , 2009, Bioinform..
[12] W. J. Kent,et al. The UCSC Genome Browser , 2003, Current protocols in bioinformatics.
[13] Anton Nekrutenko,et al. Galaxy CloudMan: delivering cloud compute clusters , 2010, BMC Bioinformatics.
[14] H. Hakonarson,et al. ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data , 2010, Nucleic acids research.
[15] Aleksandar Milosavljevic,et al. An integrative variant analysis suite for whole exome next-generation sequencing data , 2012, BMC Bioinformatics.
[16] N. Siva. 1000 Genomes project , 2008, Nature Biotechnology.
[17] Gonçalo R. Abecasis,et al. The variant call format and VCFtools , 2011, Bioinform..
[18] M. Marra,et al. Massively parallel sequencing: the next big thing in genetic medicine. , 2009, American journal of human genetics.