Found: 9
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ArCH: improving the performance of clonal hematopoiesis variant calling and interpretation.
- Published in:
- Bioinformatics, 2024, v. 40, n. 4, p. 1, doi. 10.1093/bioinformatics/btae121
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- Article
Manta: rapid detection of structural variants and indels for germline and cancer sequencing applications.
- Published in:
- Bioinformatics, 2016, v. 32, n. 8, p. 1220, doi. 10.1093/bioinformatics/btv710
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- Publication type:
- Article
Personalized treatment of Sézary syndrome by targeting a novel CTLA4:CD28 fusion.
- Published in:
- Molecular Genetics & Genomic Medicine, 2015, v. 3, n. 2, p. 130, doi. 10.1002/mgg3.121
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- Article
Isaac: ultra-fast whole-genome secondary analysis on Illumina sequencing platforms.
- Published in:
- Bioinformatics, 2013, v. 29, n. 16, p. 2041, doi. 10.1093/bioinformatics/btt314
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- Article
Sequencing by avidity enables high accuracy with low reagent consumption.
- Published in:
- Nature Biotechnology, 2024, v. 42, n. 1, p. 132, doi. 10.1038/s41587-023-01750-7
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- Article
Distribution and Abundance of Microsatellites in the Yeast Genome Can Be Explained by a Balance Between Slippage Events and Point Mutations.
- Published in:
- Molecular Biology & Evolution, 2000, v. 17, n. 8, p. 1210, doi. 10.1093/oxfordjournals.molbev.a026404
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- Article
Low-pass sequencing plus imputation using avidity sequencing displays comparable imputation accuracy to sequencing by synthesis while reducing duplicates.
- Published in:
- G3: Genes | Genomes | Genetics, 2024, v. 14, n. 2, p. 1, doi. 10.1093/g3journal/jkad276
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- Article
The International HapMap Project.
- Published in:
- Nature, 2003, v. 426, n. 6968, p. 789, doi. 10.1038/nature02168
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- Article
FGF12 copy number variant associated with epileptic encephalopathy.
- Published in:
- Clinical Genetics, 2024, v. 106, n. 1, p. 114, doi. 10.1111/cge.14542
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- Publication type:
- Article