David Heller
TitleCited byYear
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
202017
SVIM: structural variant identification using mapped long reads
D Heller, M Vingron
Bioinformatics 35 (17), 2907-2915, 2019
162019
Genotyping structural variants in pangenome graphs using the vg toolkit
G Hickey, D Heller, J Monlong, JA Sibbesen, J Siren, J Eizenga, ...
Genome Biology 21 (1), 1-17, 2020
42020
Efficient chromosome-scale haplotype-resolved assembly of human genomes
S Garg, AA Fungtammasan, A Carroll, M Chou, A Schmitt, X Zhou, S Mac, ...
bioRxiv, 810341, 2019
12019
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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Articles 1–5