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Native bacterial communities and Listeria monocytogenes survival in soils collected from the Lower Mainland of British Columbia, Canada.
- Published in:
- Canadian Journal of Microbiology, 2018, v. 64, n. 10, p. 695, doi. 10.1139/cjm-2018-0115
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- Article
Large-scale profiling of microRNAs for The Cancer Genome Atlas.
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- Nucleic Acids Research, 2016, v. 44, n. 1, p. e3, doi. 10.1093/nar/gkv808
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- Article
A platform for oncogenomic reporting and interpretation.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-28348-y
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- Article
The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
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- Nature Genetics, 2013, v. 45, n. 5, p. 522, doi. 10.1038/ng.2583
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- Article
Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.
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- Nature Genetics, 2012, v. 44, n. 1, p. 58, doi. 10.1038/ng.993
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- Article
Common variation at 10p12.31 near MLLT10 influences meningioma risk.
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- Nature Genetics, 2011, v. 43, n. 9, p. 825, doi. 10.1038/ng.879
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- Article
A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3).
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- Nature Genetics, 2010, v. 42, n. 12, p. 1126, doi. 10.1038/ng.696
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- Article
Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk.
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- Nature Genetics, 2010, v. 42, n. 6, p. 492, doi. 10.1038/ng.585
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- Article
A somatic reference standard for cancer genome sequencing.
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- Scientific Reports, 2016, p. 24607, doi. 10.1038/srep24607
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- Article
JAGuaR: Junction Alignments to Genome for RNA-Seq Reads.
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- PLoS ONE, 2014, v. 9, n. 7, p. 1, doi. 10.1371/journal.pone.0102398
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- Article
IMMU-03. TUMOR NECROSIS FACTOR OVERCOMES IMMUNE EVASION IN P53-MUTANT MEDULLOBLASTOMA.
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- Neuro-Oncology, 2019, v. 21, p. ii93, doi. 10.1093/neuonc/noz036.124
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- Article
Application of a Neural Network Whole Transcriptome–Based Pan-Cancer Method for Diagnosis of Primary and Metastatic Cancers.
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- JAMA Network Open, 2019, v. 2, n. 4, p. e192597, doi. 10.1001/jamanetworkopen.2019.2597
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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
Rare disruptive mutations and their contribution to the heritable risk of colorectal cancer.
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- Nature Communications, 2016, v. 7, n. 6, p. 11883, doi. 10.1038/ncomms11883
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- Article
MLLT1 YEATS domain mutations in clinically distinctive Favourable Histology Wilms tumours.
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- Nature Communications, 2015, v. 6, n. 12, p. 10013, doi. 10.1038/ncomms10013
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- Article
Increasing quality, throughput and speed of sample preparation for strand-specific messenger RNA sequencing.
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- BMC Genomics, 2017, v. 18, p. 1, doi. 10.1186/s12864-017-3900-6
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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
Chromosome 7p11.2 (EGFR) variation influences glioma risk.
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- Human Molecular Genetics, 2011, v. 20, n. 14, p. 2897, doi. 10.1093/hmg/ddr192
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- Article
The silent mutational landscape of infant MLL-AF4 pro-B acute lymphoblastic leukemia.
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- Genes, Chromosomes & Cancer, 2013, v. 52, n. 10, p. 954, doi. 10.1002/gcc.22090
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- Article
Sources of erroneous sequences and artifact chimeric reads in next generation sequencing of genomic DNA from formalin-fixed paraffin-embedded samples.
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- Nucleic Acids Research, 2019, v. 47, n. 2, p. e12, doi. 10.1093/nar/gky1142
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- Article
Fine-scale mapping of the 6p25.3 chronic lymphocytic leukaemia susceptibility locus.
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- Human Molecular Genetics, 2010, v. 19, n. 9, p. 1840, doi. 10.1093/hmg/ddq044
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- Article
Whole genome and transcriptome integrated analyses guide clinical care of pediatric poor prognosis cancers.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-48363-5
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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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MAVIS: merging, annotation, validation, and illustration of structural variants.
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- Bioinformatics, 2019, v. 35, n. 3, p. 515, doi. 10.1093/bioinformatics/bty621
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- Article
Automated high throughput nucleic acid purification from formalin-fixed paraffin-embedded tissue samples for next generation sequence analysis.
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- PLoS ONE, 2017, v. 12, n. 6, p. 1, doi. 10.1371/journal.pone.0178706
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- Article