Found: 75
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VISTA : visualizing global DNA sequence alignments of arbitrary length.
- Published in:
- Bioinformatics, 2000, v. 16, n. 11, p. 1046, doi. 10.1093/bioinformatics/16.11.1046
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- Publication type:
- Article
A genome-wide approach to identifying novel-imprinted genes.
- Published in:
- Human Genetics, 2008, v. 122, n. 6, p. 625, doi. 10.1007/s00439-007-0440-1
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- Publication type:
- Article
Evaluation of the SNP tagging approach in an independent population sample—array-based SNP discovery in Sami.
- Published in:
- Human Genetics, 2007, v. 122, n. 2, p. 141, doi. 10.1007/s00439-007-0379-2
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- Publication type:
- Article
Fine mapping spatiotemporal mechanisms of genetic variants underlying cardiac traits and disease.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-36638-2
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- Publication type:
- Article
Author Correction: Fine mapping spatiotemporal mechanisms of genetic variants underlying cardiac traits and disease.
- Published in:
- 2023
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- Publication type:
- Correction Notice
Fine mapping spatiotemporal mechanisms of genetic variants underlying cardiac traits and disease.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-36638-2
- By:
- Publication type:
- Article
Detection of low prevalence somatic mutations in solid tumors with ultra-deep targeted sequencing.
- Published in:
- Genome Biology, 2011, v. 12, n. 12, p. 1, doi. 10.1186/gb-2011-12-12-r124
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- Publication type:
- Article
The Genomics Gold Rush.
- Published in:
- 2007
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- Publication type:
- Editorial
Genomics Links Inflammation With Neurocognitive Impairment in Children Living With Human Immunodeficiency Virus Type-1.
- Published in:
- 2021
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- Publication type:
- journal article
Human genetic variation and its contribution to complex traits.
- Published in:
- 2009
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- Publication type:
- journal article
Identifying DNase I hypersensitive sites as driver distal regulatory elements in breast cancer.
- Published in:
- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00100-x
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- Publication type:
- Article
PTEN regulates glioblastoma oncogenesis through chromatin-associated complexes of DAXX and histone H3.3.
- Published in:
- Nature Communications, 2017, v. 8, n. 5, p. 15223, doi. 10.1038/ncomms15223
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- Publication type:
- Article
MiningABs: mining associated biomarkers across multi-connected gene expression datasets.
- Published in:
- BMC Bioinformatics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2105-15-173
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- Publication type:
- Article
Effective filtering strategies to improve data quality from population-based whole exome sequencing studies.
- Published in:
- BMC Bioinformatics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2105-15-125
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- Publication type:
- Article
In heart failure reactivation of RNA-binding proteins is associated with the expression of 1,523 fetal-specific isoforms.
- Published in:
- PLoS Computational Biology, 2022, v. 18, n. 2, p. 1, doi. 10.1371/journal.pcbi.1009918
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- Publication type:
- Article
9p21 DNA variants associated with coronary artery disease impair interferon-? signalling response.
- Published in:
- Nature, 2011, v. 470, n. 7333, p. 264, doi. 10.1038/nature09753
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- Publication type:
- Article
A second generation human haplotype map of over 3.1 million SNPs.
- Published in:
- Nature, 2007, v. 449, n. 7164, p. 851, doi. 10.1038/nature06258
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- Publication type:
- Article
A sequence-based variation map of 8.27 million SNPs in inbred mouse strains.
- Published in:
- Nature, 2007, v. 448, n. 7157, p. 1050, doi. 10.1038/nature06067
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- Publication type:
- Article
Efficient Prioritization of Multiple Causal eQTL Variants via Sparse Polygenic Modeling.
- Published in:
- Genetics, 2017, v. 207, n. 4, p. 1301, doi. 10.1534/genetics.117.300435
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- Publication type:
- Article
Erratum: Elucidating the role of 8q24 in colorectal cancer.
- Published in:
- 2009
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- Publication type:
- Correction notice
Elucidating the role of 8q24 in colorectal cancer.
- Published in:
- Nature Genetics, 2009, v. 41, n. 8, p. 868, doi. 10.1038/ng0809-868
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- Publication type:
- Article
Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides.
- Published in:
- Nature Genetics, 2008, v. 40, n. 2, p. 149, doi. 10.1038/ng.2007.61
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- Publication type:
- Article
New models of collaboration in genome-wide association studies: the Genetic Association Information Network.
- Published in:
- Nature Genetics, 2007, v. 39, n. 9, p. 1045, doi. 10.1038/ng2127
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- Publication type:
- Article
The resequencing imperative.
- Published in:
- Nature Genetics, 2007, v. 39, n. 4, p. 439, doi. 10.1038/ng0407-439
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- Publication type:
- Article
Common deletions and SNPs are in linkage disequilibrium in the human genome.
- Published in:
- Nature Genetics, 2006, v. 38, n. 1, p. 82, doi. 10.1038/ng1695
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- Publication type:
- Article
Fine-scale recombination patterns differ between chimpanzees and humans.
- Published in:
- Nature Genetics, 2005, v. 37, n. 4, p. 429, doi. 10.1038/ng1529
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- Publication type:
- Article
Pgltools: a genomic arithmetic tool suite for manipulation of Hi-C peak and other chromatin interaction data.
- Published in:
- BMC Bioinformatics, 2017, v. 18, p. 1, doi. 10.1186/s12859-017-1621-0
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- Publication type:
- Article
Allele-Specific KRT1 Expression Is a Complex Trait.
- Published in:
- PLoS Genetics, 2006, v. 2, n. 6, p. e93, doi. 10.1371/journal.pgen.0020093
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- Publication type:
- Article
Systematic genetic analysis of the MHC region reveals mechanistic underpinnings of HLA type associations with disease.
- Published in:
- eLife, 2019, p. 1, doi. 10.7554/eLife.48476
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- Publication type:
- Article
Pancreatic islet chromatin accessibility and conformation reveals distal enhancer networks of type 2 diabetes risk.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-09975-4
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- Publication type:
- Article
Subtle changes in chromatin loop contact propensity are associated with differential gene regulation and expression.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-019-08940-5
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- Publication type:
- Article
Whole Genome Sequencing Revealed Mutations in Two Independent Genes as the Underlying Cause of Retinal Degeneration in an Ashkenazi Jewish Pedigree.
- Published in:
- Genes, 2017, v. 8, n. 9, p. 210, doi. 10.3390/genes8090210
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- Publication type:
- Article
Microdroplet-based PCR enrichment for large-scale targeted sequencing.
- Published in:
- 2010
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- Publication type:
- Correction notice
Microdroplet-based PCR enrichment for large-scale targeted sequencing.
- Published in:
- Nature Biotechnology, 2009, v. 27, n. 11, p. 1025, doi. 10.1038/nbt.1583
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- Publication type:
- Article
Variation in conserved non-coding sequences on chromosome 5q and susceptibility to asthma and atopy.
- Published in:
- Respiratory Research, 2005, v. 6, p. 145, doi. 10.1186/1465-9921-6-145
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- Publication type:
- Article
Revealing sequence variation patterns in rice with machine learning methods.
- Published in:
- BMC Bioinformatics, 2008, v. 9, p. 1, doi. 10.1186/1471-2105-9-S10-O8
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- Publication type:
- Article
Transcriptome Sequencing Reveals Potential Mechanism of Cryptic 3’ Splice Site Selection in SF3B1-mutated Cancers.
- Published in:
- PLoS Computational Biology, 2015, v. 11, n. 3, p. 1, doi. 10.1371/journal.pcbi.1004105
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- Publication type:
- Article
A Covering Method for Detecting Genetic Associations between Rare Variants and Common Phenotypes.
- Published in:
- PLoS Computational Biology, 2010, v. 6, n. 10, p. 1, doi. 10.1371/journal.pcbi.1000954
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- Publication type:
- Article
Author Correction: Cellular deconvolution of GTEx tissues powers discovery of disease and cell-type associated regulatory variants.
- Published in:
- 2020
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- Publication type:
- Correction Notice
Whole Transcriptome Sequencing Enables Discovery and Analysis of Viruses in Archived Primary Central Nervous System Lymphomas.
- Published in:
- PLoS ONE, 2013, v. 8, n. 9, p. 1, doi. 10.1371/journal.pone.0073956
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- Publication type:
- Article
Transcriptome Sequencing of Tumor Subpopulations Reveals a Spectrum of Therapeutic Options for Squamous Cell Lung Cancer.
- Published in:
- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0058714
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- Publication type:
- Article
High-Resolution Mutational Profiling Suggests the Genetic Validity of Glioblastoma Patient-Derived Pre-Clinical Models.
- Published in:
- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0056185
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- Publication type:
- Article
Brief Report: Oxidative Stress Mediates Cardiomyocyte Apoptosis in a Human Model of Danon Disease and Heart Failure.
- Published in:
- Stem Cells, 2015, v. 33, n. 7, p. 2343, doi. 10.1002/stem.2015
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- Publication type:
- Article
Functional screening of an asthma QTL in YAC transgenic mice.
- Published in:
- Nature Genetics, 1999, v. 23, n. 2, p. 241, doi. 10.1038/13880
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- Publication type:
- Article
BAP1 mutation is a frequent somatic event in peritoneal malignant mesothelioma.
- Published in:
- Journal of Translational Medicine, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s12967-015-0485-1
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- Publication type:
- Article
An RNA editing fingerprint of cancer stem cell reprogramming.
- Published in:
- Journal of Translational Medicine, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s12967-014-0370-3
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- Publication type:
- Article
BAP1 mutation is a frequent somatic event in peritoneal malignant mesothelioma.
- Published in:
- 2015
- By:
- Publication type:
- journal article
An RNA editing fingerprint of cancer stem cell reprogramming.
- Published in:
- 2015
- By:
- Publication type:
- journal article
IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis.
- Published in:
- Human Genetics, 2018, v. 137, n. 6/7, p. 447, doi. 10.1007/s00439-018-1897-9
- By:
- Publication type:
- Article
Ultra‐Sharp Nanowire Arrays Natively Permeate, Record, and Stimulate Intracellular Activity in Neuronal and Cardiac Networks.
- Published in:
- Advanced Functional Materials, 2022, v. 32, n. 8, p. 1, doi. 10.1002/adfm.202108378
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- Publication type:
- Article