Towards population-scale long-read sequencing von De Coster, Wouter, Weissensteiner, Matthias H., Sedlazeck, Fritz J.

Volltext

Structural variant calling: the long and the short of it von Mahmoud, Medhat, Gobet, Nastassia, Cruz-Dávalos, Diana Ivette, Mounier, Ninon, Dessimoz, Christophe, Sedlazeck, Fritz J

Volltext

GenomeScope: fast reference-free genome profiling from short reads von Vurture, Gregory W, Sedlazeck, Fritz J, Nattestad, Maria, Underwood, Charles J, Fang, Han, Gurtowski, James, Schatz, Michael C

Volltext

NextGenMap: fast and accurate read mapping in highly polymorphic genomes von Sedlazeck, Fritz J, Rescheneder, Philipp, von Haeseler, Arndt

Volltext

The corticotopic organization of the human basal forebrain as revealed by regionally selective functional connectivity profiles von Fritz, Hans‐Christian J., Ray, Nicola, Dyrba, Martin, Sorg, Christian, Teipel, Stefan, Grothe, Michel J.

Volltext

Piercing the dark matter: bioinformatics of long-range sequencing and mapping von Sedlazeck, Fritz J., Lee, Hayan, Darby, Charlotte A., Schatz, Michael C.

Volltext

Accurate detection of complex structural variations using single-molecule sequencing von Sedlazeck, Fritz J., Rescheneder, Philipp, Smolka, Moritz, Fang, Han, Nattestad, Maria, von Haeseler, Arndt, Schatz, Michael C.

Volltext

RaGOO: fast and accurate reference-guided scaffolding of draft genomes von Alonge, Michael, Soyk, Sebastian, Ramakrishnan, Srividya, Wang, Xingang, Goodwin, Sara, Sedlazeck, Fritz J, Lippman, Zachary B, Schatz, Michael C

Volltext

Transient structural variations have strong effects on quantitative traits and reproductive isolation in fission yeast von Jeffares, Daniel C., Jolly, Clemency, Hoti, Mimoza, Speed, Doug, Shaw, Liam, Rallis, Charalampos, Balloux, Francois, Dessimoz, Christophe, Bähler, Jürg, Sedlazeck, Fritz J.

Volltext

A multi-task convolutional deep neural network for variant calling in single molecule sequencing von Luo, Ruibang, Sedlazeck, Fritz J., Lam, Tak-Wah, Schatz, Michael C.

Volltext

Smooth and clumpy dust distributions in AGN: a direct comparison of two commonly explored infrared emission models von Feltre, A., Hatziminaoglou, E., Fritz, J., Franceschini, A.

Volltext

DustPedia: Multiwavelength photometry and imagery of 875 nearby galaxies in 42 ultraviolet-microwave bands von Clark, C. J. R., Verstocken, S., Bianchi, S., Fritz, J., Viaene, S., Smith, M. W. L., Baes, M., Casasola, V., Cassara, L. P., Davies, J. I., De Looze, I., De Vis, P., Evans, R., Galametz, M., Jones, A. P., Lianou, S., Madden, S., Mosenkov, A. V., Xilouris, M.

Volltext

Truvari: refined structural variant comparison preserves allelic diversity von English, Adam C, Menon, Vipin K, Gibbs, Richard A, Metcalf, Ginger A, Sedlazeck, Fritz J

Volltext

Herschel-ATLAS: the connection between star formation and AGN activity in radio-loud and radio-quiet active galaxies von Gürkan, G., Hardcastle, M. J., Jarvis, M. J., Smith, D. J. B., Bourne, N., Dunne, L., Maddox, S., Ivison, R. J., Fritz, J.

Volltext

The ISM scaling relations in DustPedia late-type galaxies: A benchmark study for the Local Universe von Casasola, V., Bianchi, S., De Vis, P., Magrini, L., Corbelli, E., Clark, C. J. R., Fritz, J., Nersesian, A., Viaene, S., Baes, M., Cassarà, L. P., Davies, J., De Looze, I., Dobbels, W., Galametz, M., Galliano, F., Jones, A. P., Madden, S. C., Mosenkov, A. V., Trčka, A., Xilouris, E.

Volltext

Targeted nanopore sequencing with Cas9-guided adapter ligation von Gilpatrick, Timothy, Lee, Isac, Graham, James E., Raimondeau, Etienne, Bowen, Rebecca, Heron, Andrew, Downs, Bradley, Sukumar, Saraswati, Sedlazeck, Fritz J, Timp, Winston

Volltext

Multiple genome alignment in the telomere-to-telomere assembly era von Kille, Bryce, Balaji, Advait, Sedlazeck, Fritz J., Nute, Michael, Treangen, Todd J.

Volltext

Towards accurate and reliable resolution of structural variants for clinical diagnosis von Liu, Zhichao, Roberts, Ruth, Mercer, Timothy R, Xu, Joshua, Sedlazeck, Fritz J, Tong, Weida

Volltext

Inference of phylogenetic trees directly from raw sequencing reads using Read2Tree von Dylus, David, Altenhoff, Adrian, Majidian, Sina, Sedlazeck, Fritz J., Dessimoz, Christophe

Volltext

Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes von Shafin, Kishwar, Pesout, Trevor, Lorig-Roach, Ryan, Haukness, Marina, Olsen, Hugh E., Bosworth, Colleen, Armstrong, Joel, Tigyi, Kristof, Maurer, Nicholas, Koren, Sergey, Sedlazeck, Fritz J., Marschall, Tobias, Mayes, Simon, Costa, Vania, Zook, Justin M., Liu, Kelvin J., Kilburn, Duncan, Sorensen, Melanie, Munson, Katy M., Vollger, Mitchell R., Monlong, Jean, Garrison, Erik, Eichler, Evan E., Salama, Sofie, Haussler, David, Green, Richard E., Akeson, Mark, Phillippy, Adam, Miga, Karen H., Carnevali, Paolo, Jain, Miten, Paten, Benedict

Volltext