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David Heller
David Heller
Bestätigte E-Mail-Adresse bei molgen.mpg.de
Titel
Zitiert von
Zitiert von
Jahr
SVIM: structural variant identification using mapped long reads
D Heller, M Vingron
Bioinformatics 35 (17), 2907-2915, 2019
2622019
Genotyping structural variants in pangenome graphs using the vg toolkit
G Hickey, D Heller, J Monlong, JA Sibbesen, J Sirén, J Eizenga, ...
Genome biology 21, 1-17, 2020
1902020
Chromosome-scale, haplotype-resolved assembly of human genomes
S Garg, A Fungtammasan, A Carroll, M Chou, A Schmitt, X Zhou, S Mac, ...
Nature Biotechnology, 1-4, 2020
1622020
SVIM-asm: Structural variant detection from haploid and diploid genome assemblies
D Heller, M Vingron
bioRxiv, 2020
942020
The mole genome reveals regulatory rearrangements associated with adaptive intersexuality
F M. Real, SA Haas, P Franchini, P Xiong, O Simakov, H Kuhl, R Schöpflin, ...
Science 370 (6513), 208-214, 2020
492020
ssHMM: extracting intuitive sequence-structure motifs from high-throughput RNA-binding protein data
D Heller, R Krestel, U Ohler, M Vingron, A Marsico
Nucleic Acids Research 45 (19), 11004–11018, 2017
402017
Ranbow: a fast and accurate method for polyploid haplotype reconstruction
MH Moeinzadeh, J Yang, E Muzychenko, G Gallone, D Heller, K Reinert, ...
PLOS Computational Biology 16 (5), e1007843, 2020
272020
Integration of Hi-C with short and long-read genome sequencing reveals the structure of germline rearranged genomes
R Schöpflin, US Melo, H Moeinzadeh, D Heller, V Laupert, J Hertzberg, ...
Nature Communications 13 (1), 6470, 2022
222022
SDip: A novel graph-based approach to haplotype-aware assembly based structural variant calling in targeted segmental duplications sequencing
D Heller, M Vingron, G Church, H Li, S Garg
BioRxiv, 2020.02. 25.964445, 2020
152020
Structural variant calling using third-generation sequencing data
D Heller
Transcriptional Regulation (Martin Vingron), Dept. of Computational …, 2021
12021
Linear: a framework to enable existing software to resolve structural variants in long reads with flexible and efficient alignment-free statistical models
C Pan, R Rahn, D Heller, K Reinert
Briefings in Bioinformatics 24 (2), bbad071, 2023
2023
Integration of Hi-C and long-read sequencing reveals the structure of highly rearranged chromosomes in patients with germline-chromothripsis
R Schoepflin, US Melo, H Moeinzadeh, D Heller, V Heinrich, J Herztberg, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 82-82, 2022
2022
Germline chromothripsis: Integration of Hi-C and long-read sequencing reveals the structure of highly rear-ranged chromosomes
R Schopflin, US Melo, D Heller, J Jungnitsch, M Klever, M Holtgrewe, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 566-567, 2020
2020
Using multiple sequencing platforms to identify and characterise disease-causing genome alterations
G Gallone, R Schoepflin, H Moeinzadeh, D Heller, M Spielmann, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1718-1718, 2019
2019
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