Found: 17
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Association Analysis of Common Structural Variants in the Alzheimer's Disease Sequencing Project.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.078821
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- Article
Association Analysis of Common Structural Variants in the Alzheimer's Disease Sequencing Project.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.078821
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- Publication type:
- Article
Alexander of Alexandria, Arius, and Theological Method.
- Published in:
- Phronema, 2015, v. 30, n. 1, p. 1
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- Article
xAtlas: scalable small variant calling across heterogeneous next-generation sequencing experiments.
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- GigaScience, 2023, v. 12, n. 1, p. 1, doi. 10.1093/gigascience/giac125
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- Article
Mind the Gap: Upgrading Genomes with Pacific Biosciences RS Long-Read Sequencing Technology.
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- PLoS ONE, 2012, v. 7, n. 11, p. 1, doi. 10.1371/journal.pone.0047768
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- Article
Prevalence of alternative splicing choices in Arabidopsis thaliana.
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- BMC Plant Biology, 2010, v. 10, p. 102, doi. 10.1186/1471-2229-10-102
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- Article
PBHoney: identifying genomic variants via long-read discordance and interrupted mapping.
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- BMC Bioinformatics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2105-15-180
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- Article
"Science Cannot Stop With Science": Maurice Blondel and the Sciences.
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- Journal of the History of Ideas, 2008, v. 69, n. 2, p. 269, doi. 10.1353/jhi.2008.0015
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- Article
Against War: Views from the Underside of Modernity.
- Published in:
- 2009
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- Book Review
Deconstructing Jesus.
- Published in:
- 2001
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- Publication type:
- Book Review
What in the World is God Doing? (Book Review).
- Published in:
- 2000
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- Publication type:
- Book Review
Truvari: refined structural variant comparison preserves allelic diversity.
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- Genome Biology, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s13059-022-02840-6
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- Article
SVachra: a tool to identify genomic structural variation in mate pair sequencing data containing inward and outward facing reads.
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- BMC Genomics, 2017, v. 18, p. 29, doi. 10.1186/s12864-017-4021-y
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- Publication type:
- Article
Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-06159-4
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- Publication type:
- Article
Assessing structural variation in a personal genome--towards a human reference diploid genome.
- Published in:
- BMC Genomics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12864-015-1479-3
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- Publication type:
- Article
Assessing structural variation in a personal genome—towards a human reference diploid genome.
- Published in:
- BMC Genomics, 2015, v. 16, n. 1, p. 286, doi. 10.1186/s12864-015-1479-3
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- Publication type:
- Article
PacBio-LITS: a large-insert targeted sequencing method for characterization of human disease-associated chromosomal structural variations.
- Published in:
- BMC Genomics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12864-015-1370-2
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- Publication type:
- Article