P178
The date of interbreeding between Neandertals and modern humansThe Genomes of Oryza sativa: a history of duplicationsAncient human genomes suggest three ancestral populations for present-day EuropeansThe diploid genome sequence of an Asian individualA Draft Sequence of the Neandertal GenomeGenetic history of an archaic hominin group from Denisova Cave in SiberiaThe sequence and de novo assembly of the giant panda genomeGenome sequence of a 45,000-year-old modern human from western SiberiaA high-coverage genome sequence from an archaic Denisovan individualAccurate whole human genome sequencing using reversible terminator chemistryMapping short DNA sequencing reads and calling variants using mapping quality scoresTreeFam: 2008 UpdateA Bayesian deconvolution strategy for immunoprecipitation-based DNA methylome analysisIdentification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencingFast and accurate short read alignment with Burrows-Wheeler transformA genetic variation map for chicken with 2.8 million single-nucleotide polymorphismsTreeFam: a curated database of phylogenetic trees of animal gene familiesThe Sequence Alignment/Map format and SAMtoolsThe complete genome sequence of a Neanderthal from the Altai MountainsComplete genomes reveal signatures of demographic and genetic declines in the woolly mammothA direct characterization of human mutation based on microsatellitesInference of human population history from individual whole-genome sequencesFast and accurate long-read alignment with Burrows-Wheeler transformFermiKit: assembly-based variant calling for Illumina resequencing data.Porcine transcriptome analysis based on 97 non-normalized cDNA libraries and assembly of 1,021,891 expressed sequence tagsA cross-species alignment tool (CAT)Haplotype frequencies in a sub-region of chromosome 19q13.3, related to risk and prognosis of cancer, differ dramatically between ethnic groups.Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assemblyPseudo-Sanger sequencing: massively parallel production of long and near error-free reads using NGS technology.Tabix: fast retrieval of sequence features from generic TAB-delimited files.A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data.The anatomy of successful computational biology software.A draft sequence for the genome of the domesticated silkworm (Bombyx mori).A survey of sequence alignment algorithms for next-generation sequencing.No evidence that selection has been less effective at removing deleterious mutations in Europeans than in AfricansPigGIS: Pig Genomic Informatics System.Snap: an integrated SNP annotation platform.SOAPindel: efficient identification of indels from short paired reads.Using population admixture to help complete maps of the human genome.Evolutionary transients in the rice transcriptome.
P50
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P50
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Heng Li
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Heng Li
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Heng Li
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Heng Li
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Heng Li
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هنق لی
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P108
P1053
D-9344-2011
P106
P1153
12777127000
P21
P2456
P31
P3829
P496
0000-0003-4874-2874