Stefan Canzar

Affiliations: 
2012-2014 Institute of Genetic Medicine Johns Hopkins University, Baltimore, MD 
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"Stefan Canzar"
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Yoo D, Rhie A, Hebbar P, et al. (2024) Complete sequencing of ape genomes. Biorxiv : the Preprint Server For Biology
Greshnova A, Pál K, Martinez JFI, et al. (2024) Transcript Isoform Diversity of Y Chromosome Ampliconic Genes of Great Apes Uncovered Using Long Reads and Telomere-to-Telomere Reference Genome Assemblies. Biorxiv : the Preprint Server For Biology
Do VH, Elbassioni K, Canzar S. (2020) Sphetcher: Spherical Thresholding Improves Sketching of Single-Cell Transcriptomic Heterogeneity. Iscience. 23: 101126
Chakraborty S, Canzar S, Marschall T, et al. (2020) Chromatyping: Reconstructing Nucleosome Profiles from NOMe Sequencing Data. Journal of Computational Biology : a Journal of Computational Molecular Cell Biology. 27: 330-341
Andreotti S, Canzar S. (2019) Guided Reconstruction of Full-Length Isoforms from Short Reads by CIDANE. Methods in Molecular Biology (Clifton, N.J.). 1870: 199-208
Gonzales NM, Seo J, Hernandez Cordero AI, et al. (2018) Genome wide association analysis in a mouse advanced intercross line. Nature Communications. 9: 5162
Sulakhe D, D'Souza M, Wang S, et al. (2018) Exploring the functional impact of alternative splicing on human protein isoforms using available annotation sources. Briefings in Bioinformatics
Kuang Z, Canzar S. (2018) Tracking Alternatively Spliced Isoforms from Long Reads by SpliceHunter. Methods in Molecular Biology (Clifton, N.J.). 1751: 73-88
Canzar S, Salzberg SL. (2017) Short Read Mapping: An Algorithmic Tour. Proceedings of the Ieee. Institute of Electrical and Electronics Engineers. 105: 436-458
Canzar S, Neu KE, Tang Q, et al. (2017) BASIC: BCR assembly from single cells. Bioinformatics (Oxford, England). 33: 425-427
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