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Development of a Personalized Tumor Neoantigen Based Vaccine Formulation (FRAME-001) for Use in a Phase II Trial for the Treatment of Advanced Non-Small Cell Lung Cancer.
- Published in:
- Pharmaceutics, 2022, v. 14, n. 7, p. N.PAG, doi. 10.3390/pharmaceutics14071515
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- Publication type:
- Article
Micronuclei-based model system reveals functional consequences of chromothripsis in human cells.
- Published in:
- eLife, 2019, p. 1, doi. 10.7554/eLife.50292
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- Publication type:
- Article
Mouse microRNA profiles determined with a new and sensitive cloning method.
- Published in:
- Nucleic Acids Research, 2006, v. 34, n. 17, p. e115, doi. 10.1093/nar/gkl653
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- Publication type:
- Article
Optimizing Nanopore sequencing-based detection of structural variants enables individualized circulating tumor DNA-based disease monitoring in cancer patients.
- Published in:
- Genome Medicine, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13073-021-00899-7
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- Publication type:
- Article
Clinical and molecular characterization of an infant with a tandem duplication and deletion of 19p13.
- Published in:
- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 8, p. 1884, doi. 10.1002/ajmg.a.37076
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- Article
Genome-wide patterns and properties of de novo mutations in humans.
- Published in:
- Nature Genetics, 2015, v. 47, n. 7, p. 822, doi. 10.1038/ng.3292
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- Publication type:
- Article
In situ detection of miRNAs in animal embryos using LNA-modified oligonucleotide probes.
- Published in:
- Nature Methods, 2006, v. 3, n. 1, p. 27, doi. 10.1038/nmeth843
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- Publication type:
- Article
ViVar: A Comprehensive Platform for the Analysis and Visualization of Structural Genomic Variation.
- Published in:
- PLoS ONE, 2014, v. 9, n. 12, p. 1, doi. 10.1371/journal.pone.0113800
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- Publication type:
- Article
Author Correction: Accurate detection of circulating tumor DNA using nanopore consensus sequencing.
- Published in:
- 2023
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- Publication type:
- Correction Notice
Accurate detection of circulating tumor DNA using nanopore consensus sequencing.
- Published in:
- NPJ Genomic Medicine, 2021, v. 6, n. 1, p. 1, doi. 10.1038/s41525-021-00272-y
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- Publication type:
- Article
Distinct Genomic Profiles Are Associated with Treatment Response and Survival in Ovarian Cancer.
- Published in:
- Cancers, 2022, v. 14, n. 6, p. 1511, doi. 10.3390/cancers14061511
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- Publication type:
- Article
Mate pair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations.
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- European Journal of Human Genetics, 2014, v. 22, n. 5, p. 652, doi. 10.1038/ejhg.2013.220
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- Publication type:
- Article
Discovery of variants unmasked by hemizygous deletions.
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- European Journal of Human Genetics, 2012, v. 20, n. 7, p. 748, doi. 10.1038/ejhg.2011.263
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- Publication type:
- Article
Cloning and expression of new microRNAs from zebrafish.
- Published in:
- Nucleic Acids Research, 2006, v. 34, n. 9, p. 2558, doi. 10.1093/nar/gkl278
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- Publication type:
- Article
Substrate requirements for let-7 function in the developing zebrafish embryo.
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- Nucleic Acids Research, 2004, v. 32, n. 21, p. 6284, doi. 10.1093/nar/gkh968
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- Publication type:
- Article
Destabilized SMC5/6 complex leads to chromosome breakage syndrome with severe lung disease.
- Published in:
- 2016
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- Publication type:
- journal article
A high-quality human reference panel reveals the complexity and distribution of genomic structural variants.
- Published in:
- Nature Communications, 2016, v. 7, n. 10, p. 12989, doi. 10.1038/ncomms12989
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- Publication type:
- Article
The presence of extra chromosomes leads to genomic instability.
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- Nature Communications, 2016, v. 7, n. 2, p. 10754, doi. 10.1038/ncomms10754
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- Publication type:
- Article
Chromothripsis is a common mechanism driving genomic rearrangements in primary and metastatic colorectal cancer.
- Published in:
- Genome Biology, 2011, v. 12, n. 10, p. 1, doi. 10.1186/gb-2011-12-10-r103
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- Publication type:
- Article
Chromothripsis as a mechanism driving complex de novo structural rearrangements in the germline†.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 10, p. 1916, doi. 10.1093/hmg/ddr073
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- Publication type:
- Article
Deciphering the pathogenic consequences of chromosomal aberrations in human genetic disease.
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- Molecular Cytogenetics (17558166), 2014, v. 7, n. 1, p. 186, doi. 10.1186/s13039-014-0100-9
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- Publication type:
- Article
LPIN2 Is Associated With Type 2 Diabetes, Glucose Metabolism, and Body Composition.
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- Diabetes, 2007, v. 56, n. 12, p. 3020, doi. 10.2337/db07-0338
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- Publication type:
- Article
Targeted Inhibition of miRNA Maturation with Morpholinos Reveals a Role for miR-375 in Pancreatic Islet Development.
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- PLoS Biology, 2007, v. 5, n. 8, p. 1738, doi. 10.1371/journal.pbio.0050203
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- Publication type:
- Article
sv-callers: a highly portable parallel workflow for structural variant detection in whole-genome sequence data.
- Published in:
- PeerJ, 2020, p. 1, doi. 10.7717/peerj.8214
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- Publication type:
- Article
Mapping and phasing of structural variation in patient genomes using nanopore sequencing.
- Published in:
- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-01343-4
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- Publication type:
- Article
From squiggle to basepair: computational approaches for improving nanopore sequencing read accuracy.
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- Genome Biology, 2018, v. 19, n. 1, p. N.PAG, doi. 10.1186/s13059-018-1462-9
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- Publication type:
- Article
Gene length corrected trimmed mean of M-values (GeTMM) processing of RNA-seq data performs similarly in intersample analyses while improving intrasample comparisons.
- Published in:
- BMC Bioinformatics, 2018, v. 19, n. 1, p. 1, doi. 10.1186/s12859-018-2246-7
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- Publication type:
- Article
Multi-contact 4C: long-molecule sequencing of complex proximity ligation products to uncover local cooperative and competitive chromatin topologies.
- Published in:
- Nature Protocols, 2020, v. 15, n. 2, p. 364, doi. 10.1038/s41596-019-0242-7
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- Publication type:
- Article
Improving mammalian genome scaffolding using large insert mate-pair next-generation sequencing.
- Published in:
- BMC Genomics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2164-14-257
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- Publication type:
- Article
Partner independent fusion gene detection by multiplexed CRISPR-Cas9 enrichment and long read nanopore sequencing.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-16641-7
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- Publication type:
- Article
Prioritization of genes driving congenital phenotypes of patients with de novo genomic structural variants.
- Published in:
- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0692-0
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- Publication type:
- Article
Molecular dissection of germline chromothripsis in a developmental context using patient-derived iPS cells.
- Published in:
- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0399-z
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- Publication type:
- Article
High mRNA expression of splice variant SYK short correlates with hepatic disease progression in chemonaive lymph node negative colon cancer patients.
- Published in:
- PLoS ONE, 2017, v. 12, n. 9, p. 1, doi. 10.1371/journal.pone.0185607
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- Publication type:
- Article