User profiles for Danang Crysnanto

Danang Crysnanto

Senior Data Scientist, Bioinformatics, AstraZeneca
Verified email at astrazeneca.com
Cited by 315

[HTML][HTML] Bovine breed-specific augmented reference graphs facilitate accurate sequence read mapping and unbiased variant discovery

D Crysnanto, H Pausch - Genome biology, 2020 - Springer
Background The current bovine genomic reference sequence was assembled from a
Hereford cow. The resulting linear assembly lacks diversity because it does not contain allelic …

[HTML][HTML] Assessing genomic diversity and signatures of selection in Original Braunvieh cattle using whole-genome sequencing data

M Bhati, NK Kadri, D Crysnanto, H Pausch - BMC genomics, 2020 - Springer
Background Autochthonous cattle breeds are an important source of genetic variation
because they might carry alleles that enable them to adapt to local environment and food …

[HTML][HTML] Structural variant-based pangenome construction has low sensitivity to variability of haplotype-resolved bovine assemblies

AS Leonard, D Crysnanto, ZH Fang, MP Heaton… - Nature …, 2022 - nature.com
Advantages of pangenomes over linear reference assemblies for genome research have
recently been established. However, potential effects of sequence platform and assembly …

[HTML][HTML] Graph construction method impacts variation representation and analyses in a bovine super-pangenome

AS Leonard, D Crysnanto, XM Mapel, M Bhati… - Genome Biology, 2023 - Springer
Background Several models and algorithms have been proposed to build pangenomes
from multiple input assemblies, but their impact on variant representation, and consequently …

Novel functional sequences uncovered through a bovine multiassembly graph

D Crysnanto, AS Leonard, ZH Fang… - Proceedings of the …, 2021 - National Acad Sciences
Many genomic analyses start by aligning sequencing reads to a linear reference genome.
However, linear reference genomes are imperfect, lacking millions of bases of unknown …

[HTML][HTML] Accurate sequence variant genotyping in cattle using variation-aware genome graphs

D Crysnanto, C Wurmser, H Pausch - Genetics Selection Evolution, 2019 - Springer
Background Genotyping of sequence variants typically involves, as a first step, the alignment
of sequencing reads to a linear reference genome. Because a linear reference genome …

[HTML][HTML] Structural variation and introgression from wild populations in East Asian cattle genomes confer adaptation to local environment

…, L Peng, Z Dong, H Pausch, AS Leonard, D Crysnanto… - Genome Biology, 2023 - Springer
Background Structural variations (SVs) in individual genomes are major determinants of
complex traits, including adaptability to environmental variables. The Mongolian and Hainan …

[HTML][HTML] Characterization of a haplotype-reference panel for genotyping by low-pass sequencing in Swiss Large White pigs

A Nosková, M Bhati, NK Kadri, D Crysnanto… - BMC genomics, 2021 - Springer
Background The key-ancestor approach has been frequently applied to prioritize individuals
for whole-genome sequencing based on their marginal genetic contribution to current …

[HTML][HTML] Activation of cryptic splicing in bovine WDR19 is associated with reduced semen quality and male fertility

M Hiltpold, G Niu, NK Kadri, D Crysnanto, ZH Fang… - PLoS …, 2020 - journals.plos.org
Cattle are ideally suited to investigate the genetics of male reproduction, because semen
quality and fertility are recorded for all ejaculates of artificial insemination bulls. We analysed …

[HTML][HTML] Widespread gene duplication and adaptive evolution in the RNA interference pathways of the Drosophila obscura group

D Crysnanto, DJ Obbard - BMC evolutionary biology, 2019 - Springer
Background RNA interference (RNAi) related pathways provide defense against viruses
and transposable elements, and have been implicated in the suppression of meiotic drive …