Found: 19
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A Scalable Strand-Specific Protocol Enabling Full-Length Total RNA Sequencing From Single Cells.
- Published in:
- Frontiers in Genetics, 2021, v. 11, p. 1, doi. 10.3389/fgene.2021.665888
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- Article
A Distributed Whole Genome Sequencing Benchmark Study.
- Published in:
- Frontiers in Genetics, 2020, v. 11, p. N.PAG, doi. 10.3389/fgene.2020.612515
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- Publication type:
- Article
A platform for oncogenomic reporting and interpretation.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-28348-y
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- Article
A clinical transcriptome approach to patient stratification and therapy selection in acute myeloid leukemia.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-22625-y
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- Article
The transcriptional landscape of Shh medulloblastoma.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-21883-0
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- Publication type:
- Article
Complete genomic landscape of a recurring sporadic parathyroid carcinoma.
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- Journal of Pathology, 2013, v. 230, n. 3, p. 249, doi. 10.1002/path.4203
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- Article
Comparative analysis of the genome sequences of Bordetella pertussis, Bordetella parapertussis and Bordetella bronchiseptica.
- Published in:
- Nature Genetics, 2003, v. 35, n. 1, p. 32, doi. 10.1038/ng1227
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- Article
MEN1 mutations in Hürthle cell (oncocytic) thyroid carcinoma.
- Published in:
- 2015
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- Publication type:
- journal article
Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma.
- Published in:
- Nature, 2011, v. 476, n. 7360, p. 298, doi. 10.1038/nature10351
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- Publication type:
- Article
Enhancing clinical genomic accuracy with panelGC: a novel metric and tool for quantifying and monitoring GC biases in hybridization capture panel sequencing.
- Published in:
- Briefings in Bioinformatics, 2024, v. 25, n. 5, p. 1, doi. 10.1093/bib/bbae442
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- Article
Genomic analyses identify recurrent MEF2D fusions in acute lymphoblastic leukaemia.
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- Nature Communications, 2016, v. 7, n. 11, p. 13331, doi. 10.1038/ncomms13331
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- Article
Comprehensive whole genome sequence analyses yields novel genetic and structural insights for Intellectual Disability.
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- BMC Genomics, 2017, v. 18, p. 1, doi. 10.1186/s12864-017-3671-0
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- Article
Whole genome and whole transcriptome genomic profiling of a metastatic eccrine porocarcinoma.
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- NPJ Precision Oncology, 2018, v. 2, n. 1, p. N.PAG, doi. 10.1038/s41698-018-0050-5
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- Article
The Genome of the Beluga Whale (Delphinapterus leucas).
- Published in:
- Genes, 2017, v. 8, n. 12, p. 378, doi. 10.3390/genes8120378
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- Publication type:
- Article
The Genome of the Northern Sea Otter (Enhydra lutris kenyoni).
- Published in:
- Genes, 2017, v. 8, n. 12, p. 379, doi. 10.3390/genes8120379
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- Article
Barnacle: detecting and characterizing tandem duplications and fusions in transcriptome assemblies.
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- BMC Genomics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2164-14-550
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- Article
Genomic and Cytogenetic Characterization of a Balanced Translocation Disrupting NUP98.
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- Cytogenetic & Genome Research, 2017, v. 152, n. 3, p. 117, doi. 10.1159/000479463
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- Article
MAVIS: merging, annotation, validation, and illustration of structural variants.
- Published in:
- Bioinformatics, 2019, v. 35, n. 3, p. 515, doi. 10.1093/bioinformatics/bty621
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- Publication type:
- Article
BreakFusion: targeted assembly-based identification of gene fusions in whole transcriptome paired-end sequencing data.
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- Bioinformatics, 2012, v. 28, n. 14, p. 1923, doi. 10.1093/bioinformatics/bts272
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- Article