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  • Showing 1-16 of 16 Results
2014
Rictor/mTORC2 Loss in the Myf5 Lineage Reprograms Brown Fat Metabolism and Protects Mice against Obesity and Metabolic Disease.Hung, CM, Calejman CM, Sanchez-Gurmaches J., Li H., Clish CB, Hettmer S., Wagers AJ, and Guertin DA Cell reports, 2014/07/10, Volume 8, Issue 1, p.256-71, (2014) Read More / View Supplemental Materials
Abstract
Toward better understanding of artifacts in variant calling from high-coverage samples.Li, H. Bioinformatics (Oxford, England), 2014/06/27, (2014) Read More / View Supplemental Materials
Abstract
Triplication of a 21q22 region contributes to B cell transformation through HMGN1 overexpression and loss of histone H3 Lys27 trimethylation.Lane, AA, Chapuy B., Lin CY, Tivey T., Li H., Townsend EC, van Bodegom D., Day TA, Wu SC, Liu H., Yoda A., Alexe G., Schinzel AC, Sullivan TJ, Malinge S., Taylor JE, Stegmaier K., Jaffe JD, Bustin M., Te Kronnie G., et al. Nature genetics, 2014/04/20, (2014) Read More / View Supplemental Materials
Abstract
The complete genome sequence of a Neanderthal from the Altai Mountains.Prüfer, K., Racimo F., Patterson N., Jay F., Sankararaman S., Sawyer S., Heinze A., Renaud G., Sudmant PH, de Filippo C., Li H., Mallick S., Dannemann M., Fu Q., Kircher M., Kuhlwilm M., Lachmann M., Meyer M., Ongyerth M., Siebauer M., et al. Nature, 2014/01/02, Volume 505, Issue 7481, p.43-9, (2014) Read More / View Supplemental Materials
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2013
Mapping the Human Reference Genome's Missing Sequence by Three-Way Admixture in Latino Genomes.Genovese, G., Handsaker RE, Li H., Kenny EE, and McCarroll SA American journal of human genetics, 2013/09/05, Volume 93, Issue 3, p.411-21, (2013) Read More / View Supplemental Materials
Abstract
Using population admixture to help complete maps of the human genome.Genovese, G., Handsaker RE, Li H., Altemose N., Lindgren AM, Chambert K., Pasaniuc B., Price AL, Reich D., Morton CC, Pollak MR, Wilson JG, and McCarroll SA Nature genetics, 2013/02/24, (2013) Read More / View Supplemental Materials
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2012
The Date of Interbreeding between Neandertals and Modern Humans.Sankararaman, S., Patterson N., Li H., Pääbo S., and Reich D. PLoS genetics, 2012/10/01, Volume 8, Issue 10, p.e1002947, (2012) Read More / View Supplemental Materials
Abstract
Extremely low-coverage sequencing and imputation increases power for genome-wide association studies.Pasaniuc, B., Rohland N., McLaren PJ, Garimella K., Zaitlen N., Li H., Gupta N., Neale BM, Daly M. J., Sklar P., Sullivan PF, Bergen S., Moran JL, Hultman CM, Lichtenstein P., Magnusson P., Purcell SM, Haas DW, Liang L., Sunyaev S., et al. Nature genetics, 2012/05/20, Volume 44, Issue 6, p.631-5, (2012) Read More / View Supplemental Materials
Abstract
Exploring single-sample SNP and INDEL calling with whole-genome de novo assembly.Li, H. Bioinformatics (Oxford, England), 2012/05/07, (2012) Read More / View Supplemental Materials
Abstract
pIRS: Profile based Illumina pair-end Reads Simulator.Hu, X., Yuan J., Shi Y., Lu J., Liu B., Li Z., Chen Y., Mu D., Zhang H., Li N., Yue Z., Bai F., Li H., and An WF Bioinformatics (Oxford, England), 2012/04/15, (2012) Read More / View Supplemental Materials
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2011
A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data.Li, H. Bioinformatics (Oxford, England), 2011/11/01, Volume 27, Issue 21, p.2987-93, (2011) Read More / View Supplemental Materials
Abstract
Improving SNP discovery by base alignment quality.Li, H. Bioinformatics (Oxford, England), 2011/04/15, Volume 27, Issue 8, p.1157-8, (2011) Read More / View Supplemental Materials
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Tabix: fast retrieval of sequence features from generic TAB-delimited files.Li, H. Bioinformatics (Oxford, England), 2011/03/01, Volume 27, Issue 5, p.718-9, (2011) Read More / View Supplemental Materials
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2010
A survey of sequence alignment algorithms for next-generation sequencing.Li, H., and Homer N. Briefings in bioinformatics, 2010/09/01, Volume 11, Issue 5, p.473-83, (2010) Read More / View Supplemental Materials
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A draft sequence of the Neandertal genome.Green, RE, Krause J., Briggs AW, Maricic T., Stenzel U., Kircher M., Patterson N., Li H., Zhai W., Fritz MH, Hansen NF, Durand EY, Malaspinas AS, Jensen JD, Marques-Bonet T., Alkan C., Prüfer K., Meyer M., Burbano HA, Good JM, et al. Science (New York, N.Y.), 2010/05/07, Volume 328, Issue 5979, p.710-22, (2010) Read More / View Supplemental Materials
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2009
The Sequence Alignment/Map format and SAMtools.Li, H., Handsaker B., Wysoker A., Fennell T., Ruan J., Homer N., Marth G., Abecasis G., Durbin R., and 1000 Genome Project Data Processing Subgroup Bioinformatics (Oxford, England), 2009/08/15, Volume 25, Issue 16, p.2078-9, (2009) Read More / View Supplemental Materials
Abstract
  • Showing 1-16 of 16 Results