Danang Crysnanto
Reproducibility track record
1
assessed papers
45/100
mean reproducibility
0
reproduced (C1–C2)
1
flagged
63
total citations
flag rate:
100%
(1/1)
The share of this author’s assessed papers carrying a ⚑ flag. A concentration is a prompt for expert review — never, on its own, a determination about the person.
Authorship role
first author: 1
last author: 0
Topics
Funders
—
Frequent co-authors
Institutions
ETH Zurich 1
Geography (author institutions)
CH 1
Co-author network
Collaborators, sized by shared output and coloured by their own reproducibility (green = high, red = low). Click a node to open their card. A pattern is a prompt for review, never a determination.
How this author’s assessed papers reproduced — the outcome of reproduction attempts, not a judgement of the person. Coverage is partial and grows over time.
Assessed papers (1)
Complete publication record (57)
Request a reproduction →1 assessed by us (0 reproduced) · 56 not yet assessed — every PubMed paper on record, linked below.
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Graph construction method impacts variation representation and analyses in a bovine super-pangenome ↗Genome biology · 2023 · PMID 37217946not yet assessed
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Structural variation and introgression from wild populations in East Asian cattle genomes confer adaptation to local environment ↗Genome biology · 2023 · PMID 37723525not yet assessed
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Additional file 2 of Structural variation and introgression from wild populations in East Asian cattle genomes confer adaptation to local environment ↗Open MIND · 2023not yet assessed
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Structural variant-based pangenome construction has low sensitivity to variability of haplotype-resolved bovine assemblies ↗Nature Communications · 2022 · PMID 35641504not yet assessed
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not yet assessed
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Graph construction method impacts variation representation and analyses in a bovine super-pangenome ↗bioRxiv (Cold Spring Harbor Laboratory) · 2022not yet assessed
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Novel functional sequences uncovered through a bovine multiassembly graph ↗Proceedings of the National Academy of Sciences · 2021 · PMID 33972446not yet assessed
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Characterization of a haplotype-reference panel for genotyping by low-pass sequencing in Swiss Large White pigs ↗BMC Genomics · 2021 · PMID 33882824not yet assessed
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Structural variant-based pangenome construction has low sensitivity to variability of haplotype-resolved bovine assemblies ↗bioRxiv (Cold Spring Harbor Laboratory) · 2021not yet assessed
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Novel functional sequences uncovered through a bovine multi-assembly graph ↗bioRxiv (Cold Spring Harbor Laboratory) · 2021not yet assessed
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Characterization of a haplotype-reference panel for genotyping by low-pass sequencing in Swiss Large White pigs ↗bioRxiv (Cold Spring Harbor Laboratory) · 2021not yet assessed
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Characterization of a haplotype- reference panel for genotyping by low-pass sequencing in Swiss Large White pigs ↗Research Square · 2021not yet assessed
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Additional file 3 of Characterization of a haplotype-reference panel for genotyping by low-pass sequencing in Swiss Large White pigs ↗Open MIND · 2021not yet assessed
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Additional file 5 of Characterization of a haplotype-reference panel for genotyping by low-pass sequencing in Swiss Large White pigs ↗Figshare · 2021not yet assessed
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Assessing genomic diversity and signatures of selection in Original Braunvieh cattle using whole-genome sequencing data ↗BMC Genomics · 2020 · PMID 31914939not yet assessed
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Activation of cryptic splicing in bovine WDR19 is associated with reduced semen quality and male fertility ↗PLoS Genetics · 2020 · PMID 32407316not yet assessed
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Bovine breed-specific augmented reference graphs facilitate accurate sequence read mapping and unbiased variant discovery ↗Genome biology · 2020 · PMID 32718320not yet assessed
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Deletion of porcine <i>BOLL</i> is associated with defective acrosomes and subfertility in Yorkshire boars ↗Animal Genetics · 2020 · PMID 32975846not yet assessed
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A 63‐bp insertion in exon 2 of the porcine <i>KIF21A</i> gene is associated with arthrogryposis multiplex congenita ↗Animal Genetics · 2020 · PMID 32686171not yet assessed
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Activation of cryptic splicing in bovine <i>WDR19</i> is associated with reduced semen quality and male fertility ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
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Deletion of porcine <i>BOLL</i> causes defective acrosomes and subfertility in Yorkshire boars ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
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Supporting data for Novel functional sequences uncovered through a bovine multi-assembly graph ↗Zenodo (CERN European Organization for Nuclear Research) · 2020not yet assessed
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A 63-bp insertion in exon 2 of the porcine <i>KIF21A</i> gene is associated with arthrogryposis multiplex congenita ↗bioRxiv (Cold Spring Harbor Laboratory) · 2020not yet assessed
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Mapping Sequencing Reads to Bovine Breed-Specific Genome Graphs2020not yet assessed
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Deletion of porcine BOLL causes defective acrosomes and subfertility in Yorkshire boars ↗Figshare · 2020not yet assessed
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Error upload ↗Zenodo (CERN European Organization for Nuclear Research) · 2020not yet assessed
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A 63-bp insertion in exon 2 of the porcine KIF21A gene is associated with arthrogryposis multiplex congenita ↗Zenodo (CERN European Organization for Nuclear Research) · 2020not yet assessed
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Supporting data for Novel functional sequences uncovered through a bovine multi-assembly graph ↗Zenodo (CERN European Organization for Nuclear Research) · 2020not yet assessed
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Deletion of porcine BOLL causes defective acrosomes and subfertility in Yorkshire boars ↗Figshare · 2020not yet assessed
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A 63-bp insertion in exon 2 of the porcine KIF21A gene is associated with arthrogryposis multiplex congenita ↗Zenodo (CERN European Organization for Nuclear Research) · 2020not yet assessed
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Deletion of porcine BOLL causes defective acrosomes and subfertility in Yorkshire boars ↗Zenodo (CERN European Organization for Nuclear Research) · 2020not yet assessed
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MOESM5 of Assessing genomic diversity and signatures of selection in Original Braunvieh cattle using whole-genome sequencing data ↗Figshare · 2020not yet assessed
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MOESM4 of Assessing genomic diversity and signatures of selection in Original Braunvieh cattle using whole-genome sequencing data ↗Figshare · 2020not yet assessed
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MOESM11 of Assessing genomic diversity and signatures of selection in Original Braunvieh cattle using whole-genome sequencing data ↗Figshare · 2020not yet assessed
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MOESM7 of Assessing genomic diversity and signatures of selection in Original Braunvieh cattle using whole-genome sequencing data ↗Figshare · 2020not yet assessed
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MOESM9 of Assessing genomic diversity and signatures of selection in Original Braunvieh cattle using whole-genome sequencing data ↗Figshare · 2020not yet assessed
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MOESM10 of Assessing genomic diversity and signatures of selection in Original Braunvieh cattle using whole-genome sequencing data ↗Figshare · 2020not yet assessed
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MOESM8 of Assessing genomic diversity and signatures of selection in Original Braunvieh cattle using whole-genome sequencing data ↗Figshare · 2020not yet assessed
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Additional file 3 of Bovine breed-specific augmented reference graphs facilitate accurate sequence read mapping and unbiased variant discovery ↗Open MIND · 2020not yet assessed
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MOESM12 of Assessing genomic diversity and signatures of selection in Original Braunvieh cattle using whole-genome sequencing data ↗Figshare · 2020not yet assessed
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MOESM14 of Assessing genomic diversity and signatures of selection in Original Braunvieh cattle using whole-genome sequencing data ↗Figshare · 2020not yet assessed
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Accurate sequence variant genotyping in cattle using variation-aware genome graphs⚑Genetics Selection Evolution · 2019 · PMID 31092189L1 45/100 ⚑
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Widespread gene duplication and adaptive evolution in the RNA interference pathways of the Drosophila obscura group ↗BMC Evolutionary Biology · 2019 · PMID 31068148not yet assessed
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Bovine breed-specific augmented reference graphs facilitate accurate sequence read mapping and unbiased variant discovery ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
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Data for Bovine breed-specific augmented reference graphs facilitate accurate sequence read mapping and unbiased variant discovery ↗Zenodo (CERN European Organization for Nuclear Research) · 2019not yet assessed
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Assessing genomic diversity and signatures of selection in Original Braunvieh cattle using whole-genome sequencing data ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
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Data for Bovine breed-specific augmented reference graphs facilitate accurate sequence read mapping and unbiased variant discovery ↗Zenodo (CERN European Organization for Nuclear Research) · 2019not yet assessed
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Bovine breed-specific augmented reference graphs facilitate accurate sequence read mapping and unbiased variant discovery ↗Figshare · 2019not yet assessed
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MOESM4 of Accurate sequence variant genotyping in cattle using variation-aware genome graphs ↗Figshare · 2019not yet assessed
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Additional file 3: of Widespread gene duplication and adaptive evolution in the RNA interference pathways of the Drosophila obscura group ↗Figshare · 2019not yet assessed
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Additional file 4: of Widespread gene duplication and adaptive evolution in the RNA interference pathways of the Drosophila obscura group ↗Figshare · 2019not yet assessed
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Additional file 1: of Widespread gene duplication and adaptive evolution in the RNA interference pathways of the Drosophila obscura group ↗Figshare · 2019not yet assessed
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MOESM5 of Accurate sequence variant genotyping in cattle using variation-aware genome graphs ↗Figshare · 2019not yet assessed
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Widespread gene duplication and adaptive evolution in the RNA interference pathways of the Drosophila obscura group ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
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Accurate sequence variant genotyping in cattle using variation-aware genome graphs ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
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not yet assessed
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Encapsulation of dsRNA GIH (Gonad Inhibiting Hormone) Using Chitosan Nanoparticle With Several Physiochemical Optimizations2015not yet assessed
Full bibliography from OpenAlex; reproducibility verdicts matched by PMID.
Author attribution follows OpenAlex disambiguation, which is imperfect — a researcher's papers can be split across profiles or mixed with a namesake.
Merged across profiles sharing this ORCID where present. See every “Crysnanto D” paper on PubMed ↗