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Author Correction: A benchmark of computational methods for correcting biases of established and unknown origin in CRISPR-Cas9 screening data.
- Published in:
- 2024
- By:
- Publication type:
- Correction Notice
Association Studies of BMI and Type 2 Diabetes in the Neuropeptide Y Pathway.
- Published in:
- Diabetes, 2007, v. 56, n. 5, p. 1460, doi. 10.2337/db06-1051
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- Publication type:
- Article
Estimating the human mutation rate using autozygosity in a founder population.
- Published in:
- Nature Genetics, 2012, v. 44, n. 11, p. 1277, doi. 10.1038/ng.2418
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- Publication type:
- Article
Structural diversity and African origin of the 17q21.31 inversion polymorphism.
- Published in:
- Nature Genetics, 2012, v. 44, n. 8, p. 872, doi. 10.1038/ng.2335
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- Publication type:
- Article
A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk.
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- Nature Genetics, 2010, v. 42, n. 9, p. 745, doi. 10.1038/ng.643
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- Publication type:
- Article
Demonstrating stratification in a European American population.
- Published in:
- Nature Genetics, 2005, v. 37, n. 8, p. 868, doi. 10.1038/ng1607
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- Publication type:
- Article
Next‐generation sequencing of baseline genetic mutations and outcomes of eltrombopag and azacitidine therapy in patients with myelodysplastic syndromes and thrombocytopenia: Data from the SUPPORT clinical trial.
- Published in:
- EJHaem, 2023, v. 4, n. 3, p. 876, doi. 10.1002/jha2.694
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- Publication type:
- Article
Whole-Genome Sequencing of Individuals from a Founder Population Identifies Candidate Genes for Asthma.
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- PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0104396
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- Publication type:
- Article
A benchmark of computational methods for correcting biases of established and unknown origin in CRISPR-Cas9 screening data.
- Published in:
- Genome Biology, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s13059-024-03336-1
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- Publication type:
- Article
Contribution and clinical relevance of germline variation to the cancer transcriptome.
- Published in:
- 2022
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- Publication type:
- journal article
Clonal hematopoiesis detection in patients with cancer using cell-free DNA sequencing.
- Published in:
- Science Translational Medicine, 2023, v. 15, n. 689, p. 1, doi. 10.1126/scitranslmed.abm8729
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- Publication type:
- Article
PureCN: copy number calling and SNV classification using targeted short read sequencing.
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- Source Code for Biology & Medicine, 2016, v. 11, p. 1, doi. 10.1186/s13029-016-0060-z
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- Publication type:
- Article
Association of MTOR Mutations With Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary Mosaicism.
- Published in:
- JAMA Neurology, 2016, v. 73, n. 7, p. 836, doi. 10.1001/jamaneurol.2016.0363
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- Publication type:
- Article