about
Genome sequencing highlights the dynamic early history of dogsDeath and resurrection of the human IRGM geneThe genome sequencing of an albino Western lowland gorilla reveals inbreeding in the wildA Draft Sequence of the Neandertal GenomeThe bonobo genome compared with the chimpanzee and human genomesInsights into hominid evolution from the gorilla genome sequenceGenetic history of an archaic hominin group from Denisova Cave in SiberiaComparative and demographic analysis of orang-utan genomesComplete Khoisan and Bantu genomes from southern Africa.Mapping and sequencing of structural variation from eight human genomesA high-coverage genome sequence from an archaic Denisovan individualNext-generation VariationHunter: combinatorial algorithms for transposon insertion discoveryDiversity of human copy number variation and multicopy genesMapping copy number variation by population-scale genome sequencingRefinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorderA hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTDSequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encodingManipulating multiple sequence alignments via MaM and WebMaMDemographically-Based Evaluation of Genomic Regions under Selection in Domestic DogsSCALCE: boosting sequence compression algorithms using locally consistent encodingGenome-wide characterization of centromeric satellites from multiple mammalian genomesOrganization and evolution of primate centromeric DNA from whole-genome shotgun sequence dataPersonalized copy number and segmental duplication maps using next-generation sequencing.Haplotype-resolved genome sequencing of a Gujarati Indian individual.Detection and characterization of novel sequence insertions using paired-end next-generation sequencing.mrsFAST-Ultra: a compact, SNP-aware mapper for high performance sequencing applications.Characterization of missing human genome sequences and copy-number polymorphic insertionsAnnotated features of domestic cat - Felis catus genome.A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease riskDetection of structural variants and indels within exome data.Comparative analysis of the domestic cat genome reveals genetic signatures underlying feline biology and domesticationAn integrated map of structural variation in 2,504 human genomes.Whole genome sequencing of Turkish genomes reveals functional private alleles and impact of genetic interactions with Europe, Asia and AfricaAccelerating read mapping with FastHASH.Clcn4-2 genomic structure differs between the X locus in Mus spretus and the autosomal locus in Mus musculus: AT motif enrichment on the X.Analysis of primate genomic variation reveals a repeat-driven expansion of the human genome.Alu repeat discovery and characterization within human genomesLimitations of next-generation genome sequence assemblymrsFAST: a cache-oblivious algorithm for short-read mapping.Sensitive and fast mapping of di-base encoded reads.
P50
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hulumtues
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török számítástechnikai genomika kutató
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wetenschapper
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P108
P1053
D-2982-2009
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6602505864
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P31
P3829
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