Found: 17
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Supervised dimensionality reduction for big data.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-23102-2
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- Article
Detection of low-frequency DNA variants by targeted sequencing of the Watson and Crick strands.
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- Nature Biotechnology, 2021, v. 39, n. 10, p. 1220, doi. 10.1038/s41587-021-00900-z
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- Article
Predicting survival in head and neck squamous cell carcinoma from TP53 mutation.
- Published in:
- Human Genetics, 2015, v. 134, n. 5, p. 497, doi. 10.1007/s00439-014-1470-0
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- Article
Detection of malignant peripheral nerve sheath tumors in patients with neurofibromatosis using aneuploidy and mutation identification in plasma.
- Published in:
- eLife, 2022, p. 1, doi. 10.7554/eLife.74238
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- Article
Eliminating accidental deviations to minimize generalization error and maximize replicability: Applications in connectomics and genomics.
- Published in:
- PLoS Computational Biology, 2021, v. 17, n. 9, p. 1, doi. 10.1371/journal.pcbi.1009279
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- Article
A Probabilistic Model to Predict Clinical Phenotypic Traits from Genome Sequencing.
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- PLoS Computational Biology, 2014, v. 10, n. 9, p. 1, doi. 10.1371/journal.pcbi.1003825
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- Article
A multimodality test to guide the management of patients with a pancreatic cyst.
- Published in:
- Science Translational Medicine, 2019, v. 11, n. 501, p. 1, doi. 10.1126/scitranslmed.aav4772
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- Article
Evaluation of liquid from the Papanicolaou test and other liquid biopsies for the detection of endometrial and ovarian cancers.
- Published in:
- Science Translational Medicine, 2018, v. 10, n. 433, p. 1, doi. 10.1126/scitranslmed.aap8793
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- Article
Proteins linked to autosomal dominant and autosomal recessive disorders harbor characteristic rare missense mutation distribution patterns.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 21, p. 5995, doi. 10.1093/hmg/ddv309
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- Article
Mutational Signature of Aristolochic Acid Exposure as Revealed by Whole-Exome Sequencing.
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- Science Translational Medicine, 2013, v. 5, n. 197, p. 1, doi. 10.1126/scitranslmed.3006200
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- Article
Matching phenotypes to whole genomes: Lessons learned from four iterations of the personal genome project community challenges.
- Published in:
- Human Mutation, 2017, v. 38, n. 9, p. 1266, doi. 10.1002/humu.23265
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- Article
Assessing the Pathogenicity of Insertion and Deletion Variants with the Variant Effect Scoring Tool (VEST-Indel).
- Published in:
- Human Mutation, 2016, v. 37, n. 1, p. 28, doi. 10.1002/humu.22911
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- Article
Experimental Assessment of Splicing Variants Using Expression Minigenes and Comparison with In Silico Predictions.
- Published in:
- Human Mutation, 2014, v. 35, n. 10, p. 1249, doi. 10.1002/humu.22624
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- Article
Machine learning to detect the SINEs of cancer.
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- Science Translational Medicine, 2024, v. 16, n. 731, p. 1, doi. 10.1126/scitranslmed.adi3883
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- Article
Integration of genetic and metabolic features related to sialic acid metabolism distinguishes human breast cell subtypes.
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- PLoS ONE, 2018, v. 13, n. 5, p. 1, doi. 10.1371/journal.pone.0195812
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- Article
Identifying Mendelian disease genes with the Variant Effect Scoring Tool.
- Published in:
- BMC Genomics, 2013, v. 14, n. Suppl 3, p. 1, doi. 10.1186/1471-2164-14-S3-S3
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- Publication type:
- Article
CRAVAT: cancer-related analysis of variants toolkit.
- Published in:
- Bioinformatics, 2013, v. 29, n. 5, p. 647, doi. 10.1093/bioinformatics/btt017
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- Article