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Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing. Nature genetics, 2013/03/01, Volume 45, Issue 3, p.299-303, (2013)
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Finished bacterial genomes from shotgun sequence data. Genome research, 2012/07/24, (2012)
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Paired-end sequencing of Fosmid libraries by Illumina. Genome research, 2012/07/17, (2012)
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The genomic basis of adaptive evolution in threespine sticklebacks. Nature, 2012/04/04, Volume 484, Issue 7392, p.55-61, (2012)
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Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries. Genome biology, 2012/01/09, Volume 12, Issue 2, p.R18, (2012)
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Assisted assembly: how to improve a de novo genome assembly by using related species. Genome biology, 2012/01/09, Volume 10, Issue 8, p.R88, (2012)
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A high-resolution map of human evolutionary constraint using 29 mammals. Nature, 2011/10/12, Volume 478, Issue 7370, p.476-82, (2011)
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High-quality draft assemblies of mammalian genomes from massively parallel sequence data. Proceedings of the National Academy of Sciences of the United States of America, 2011/01/25, Volume 108, Issue 4, p.1513-8, (2011)
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Integrative analysis of the melanoma transcriptome. Genome research, 2010/04/01, Volume 20, Issue 4, p.413-27, (2010)
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A scalable, fully automated process for construction of sequence-ready barcoded libraries for 454. Genome biology, 2010/02/05, Volume 11, Issue 2, p.R15, (2010)
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Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing. Nature biotechnology, 2009/02/01, Volume 27, Issue 2, p.182-9, (2009)
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ALLPATHS 2: small genomes assembled accurately and with high continuity from short paired reads. Genome biology, 2009/01/01, Volume 10, Issue 10, p.R103, (2009)
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High-resolution mapping of copy-number alterations with massively parallel sequencing. Nature methods, 2009/01/01, Volume 6, Issue 1, p.99-103, (2009)
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Sensitive, specific polymorphism discovery in bacteria using massively parallel sequencing. Nature methods, 2009/01/01, Volume 6, Issue 1, p.67-9, (2009)
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Genome-scale DNA methylation maps of pluripotent and differentiated cells. Nature, 2008/08/07, Volume 454, Issue 7205, p.766-70, (2008)
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ALLPATHS: de novo assembly of whole-genome shotgun microreads. Genome research, 2008/05/01, Volume 18, Issue 5, p.810-20, (2008)
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Quality scores and SNP detection in sequencing-by-synthesis systems. Genome research, 2008/05/01, Volume 18, Issue 5, p.763-70, (2008)
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Evolution of genes and genomes on the Drosophila phylogeny. Nature, 2007/11/08, Volume 450, Issue 7167, p.203-18, (2007)
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Genome-wide maps of chromatin state in pluripotent and lineage-committed cells. Nature, 2007/08/02, Volume 448, Issue 7153, p.553-60, (2007)
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Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project. Nature, 2007/06/14, Volume 447, Issue 7146, p.799-816, (2007)
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Analyses of deep mammalian sequence alignments and constraint predictions for 1% of the human genome. Genome research, 2007/06/01, Volume 17, Issue 6, p.760-74, (2007)
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A genome-wide map of diversity in Plasmodium falciparum. Nature genetics, 2007/01/01, Volume 39, Issue 1, p.113-9, (2007)
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DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage. Nature, 2006/04/20, Volume 440, Issue 7087, p.1045-9, (2006)
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Analysis of the DNA sequence and duplication history of human chromosome 15. Nature, 2006/03/30, Volume 440, Issue 7084, p.671-5, (2006)
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Human chromosome 11 DNA sequence and analysis including novel gene identification. Nature, 2006/03/23, Volume 440, Issue 7083, p.497-500, (2006)
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DNA sequence and analysis of human chromosome 8. Nature, 2006/01/19, Volume 439, Issue 7074, p.331-5, (2006)
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Genome sequence, comparative analysis and haplotype structure of the domestic dog. Nature, 2005/12/08, Volume 438, Issue 7069, p.803-19, (2005)
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DNA sequence and analysis of human chromosome 18. Nature, 2005/09/22, Volume 437, Issue 7058, p.551-5, (2005)
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Assembly of polymorphic genomes: algorithms and application to Ciona savignyi. Genome research, 2005/08/01, Volume 15, Issue 8, p.1127-35, (2005)
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An initial strategy for the systematic identification of functional elements in the human genome by low-redundancy comparative sequencing. Proceedings of the National Academy of Sciences of the United States of America, 2005/03/29, Volume 102, Issue 13, p.4795-800, (2005)
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