Publikationen von David Heller
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Zeitschriftenartikel (6)
1.
Zeitschriftenartikel
13 (1), 6470 (2022)
Integration of Hi-C with short and long-read genome sequencing reveals the structure of germline rearranged genomes. Nature Communications 2.
Zeitschriftenartikel
36 (22-23), S. 5519 - 5521 (2020)
SVIM-asm: structural variant detection from haploid and diploid genome assemblies. Bioinformatics 3.
Zeitschriftenartikel
370 (6513), S. 208 - 214 (2020)
The mole genome reveals regulatory rearrangements associated with adaptive intersexuality. Science 4.
Zeitschriftenartikel
16 (5), e1007843 (2020)
Ranbow: A fast and accurate method for polyploid haplotype reconstruction. PLOS Computational Biology 5.
Zeitschriftenartikel
35 (17), S. 2907 - 2915 (2019)
SVIM: Structural Variant Identification using Mapped Long Reads. Bioinformatics 6.
Zeitschriftenartikel
45 (19), S. 11004 - 11018 (2017)
ssHMM: extracting intuitive sequence-structure motifs from high-throughput RNA-binding protein data. Nucleic Acids Research (London) Hochschulschrift - Doktorarbeit (1)
7.
Hochschulschrift - Doktorarbeit
Structural variant calling using third-generation sequencing data. Dissertation, xiii, 139 S. (2021)