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Showing results 1 to 13 of 13
Year of PublicationTitleAuthor(s)Open Access
2018A graph-based approach to diploid genome assemblyGarg, Shilpa; Rautiainen, Mikko; Novak, Adam M., et al
2017A Guided Tour to Computational HaplotypingKlau, Gunnar W.; Marschall, Tobias
2019Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genomeWenger, Aaron M.; Peluso, Paul; Rowell, William J., et al
2019Bit-parallel sequence-to-graph alignmentRautiainen, Mikko; Mäkinen, Veli; Marschall, Tobias
2018Chromatyping: Reconstructing Nucleosome Profiles from NOMe Sequencing DataChakraborty, Shounak; Canzar, Stefan; Marschall, Tobias, et al
2018Computational pan-genomics: status, promises and challengesMarschall, Tobias; Marz, M.; Abeel, T., et al
2017Dense and accurate whole-chromosome haplotyping of individual genomesPorubsky, David; Garg, Shilpa; Sanders, Ashley D., et al
2019Fully-sensitive seed finding in sequence graphs using a hybrid indexGhaffaari, Ali; Marschall, Tobias
2019Genotyping inversions and tandem duplicationsEbler, Jana; Schönhuth, Alexander; Marschall, Tobias
2019Haplotype-aware diplotyping from noisy long readsEbler, Jana; Haukness, Marina; Pesout, Trevor, et al
2017Mapping and phasing of structural variation in patient genomes using nanopore sequencingCretu Stancu, Mircea; van Roosmalen, Markus J.; Renkens, Ivo, et al
2019Multi-platform discovery of haplotype-resolved structural variation in human genomesChaisson, Mark J. P.; Sanders, Ashley D.; Zhao, Xuefang, et al
2018Strand-seq enables reliable separation of long reads by chromosome via expectation maximizationGhareghani, Maryam; Porubskỳ, David; Sanders, Ashley D., et al