Found: 22
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Deciphering the exact breakpoints of structural variations using long sequencing reads with DeBreak.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-35996-1
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- Article
Selective suppression of melanoma lacking IFN-γ pathway by JAK inhibition depends on T cells and host TNF signaling.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-32754-7
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- Article
Redox-active quinones induces genome-wide DNA methylation changes by an iron-mediated and Tet-dependent mechanism.
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- Nucleic Acids Research, 2014, v. 42, n. 3, p. 1593, doi. 10.1093/nar/gkt1090
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- Article
TransVar: a multilevel variant annotator for precision genomics.
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- Nature Methods, 2015, v. 12, n. 11, p. 1002, doi. 10.1038/nmeth.3622
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- Article
Accurate long-read de novo assembly evaluation with Inspector.
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- Genome Biology, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s13059-021-02527-4
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- Article
Hotspot mutations delineating diverse mutational signatures and biological utilities across cancer types.
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- BMC Genomics, 2016, v. 17, p. 249, doi. 10.1186/s12864-016-2727-x
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- Article
Towards accurate characterization of clonal heterogeneity based on structural variation.
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- BMC Bioinformatics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2105-15-299
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- Article
The Evolution of Small Insertions and Deletions in the Coding Genes of Drosophila melanogaster.
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- Molecular Biology & Evolution, 2013, v. 30, n. 12, p. 2699, doi. 10.1093/molbev/mst167
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- Article
Ago2 facilitates Rad51 recruitment and DNA double-strand break repair by homologous recombination.
- Published in:
- Cell Research, 2014, v. 24, n. 5, p. 532, doi. 10.1038/cr.2014.36
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- Article
Clinical Actionability Enhanced through Deep Targeted Sequencing of Solid Tumors.
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- Clinical Chemistry, 2015, v. 61, n. 3, p. 544, doi. 10.1373/clinchem.2014.231100
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- Article
Functional annotation of rare gene aberration drivers of pancreatic cancer.
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- Nature Communications, 2016, v. 7, n. 1, p. 10500, doi. 10.1038/ncomms10500
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- Article
In vivo screening identifies GATAD2B as a metastasis driver in KRAS-driven lung cancer.
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- Nature Communications, 2018, v. 9, p. 1, doi. 10.1038/s41467-018-04572-3
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- Article
The genetic basis of hydrocephalus: genes, pathways, mechanisms, and global impact.
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- Fluids & Barriers of the CNS, 2024, v. 21, n. 1, p. 1, doi. 10.1186/s12987-024-00513-z
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- Article
Marker chromosome genomic structure and temporal origin implicate a chromoanasynthesis event in a family with pleiotropic psychiatric phenotypes.
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- Human Mutation, 2018, v. 39, n. 7, p. 939, doi. 10.1002/humu.23537
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- Article
Impact and characterization of serial structural variations across humans and great apes.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-52027-9
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- Article
Combining accurate tumor genome simulation with crowdsourcing to benchmark somatic structural variant detection.
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- Genome Biology, 2018, v. 19, n. 1, p. N.PAG, doi. 10.1186/s13059-018-1539-5
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- Article
ClinSeK: a targeted variant characterization framework for clinical sequencing.
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- Genome Medicine, 2015, v. 7, n. 1, p. 1, doi. 10.1186/s13073-015-0155-1
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- Article
Pseudo-Sanger sequencing: massively parallel production of long and near error-free reads using NGS technology.
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- BMC Genomics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2164-14-711
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- Article
Reduced sister chromatid cohesion acts as a tumor penetrance modifier.
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- PLoS Genetics, 2022, v. 18, n. 8, p. 1, doi. 10.1371/journal.pgen.1010341
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- Article
MRLR: unraveling high-resolution meiotic recombination by linked reads.
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- Bioinformatics, 2020, v. 36, n. 1, p. 10, doi. 10.1093/bioinformatics/btz503
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- Article
Rainbow: an integrated tool for efficient clustering and assembling RAD-seq reads.
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- Bioinformatics, 2012, v. 28, n. 21, p. 2732, doi. 10.1093/bioinformatics/bts482
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- Article
B-assembler: a circular bacterial genome assembler.
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- BMC Genomics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s12864-022-08577-7
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- Article