Works matching IS 17558794 AND DT 2018 AND VI 11
Results: 127
CRlncRC: a machine learning-based method for cancer-related long noncoding RNA identification using integrated features.
- Published in:
- BMC Medical Genomics, 2018, v. 11, n. 6, p. N.PAG, doi. 10.1186/s12920-018-0436-9
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- Publication type:
- Article
Improvement of cancer subtype prediction by incorporating transcriptome expression data and heterogeneous biological networks.
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- BMC Medical Genomics, 2018, v. 11, n. 6, p. N.PAG, doi. 10.1186/s12920-018-0435-x
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- Article
An isomiR expression panel based novel breast cancer classification approach using improved mutual information.
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- BMC Medical Genomics, 2018, v. 11, n. 6, p. N.PAG, doi. 10.1186/s12920-018-0434-y
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- Publication type:
- Article
Identification of cancer subtypes from single-cell RNA-seq data using a consensus clustering method.
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- BMC Medical Genomics, 2018, v. 11, n. 6, p. N.PAG, doi. 10.1186/s12920-018-0433-z
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- Publication type:
- Article
Discovering functional impacts of miRNAs in cancers using a causal deep learning model.
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- BMC Medical Genomics, 2018, v. 11, n. 6, p. N.PAG, doi. 10.1186/s12920-018-0432-0
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- Publication type:
- Article
Condition-specific gene co-expression network mining identifies key pathways and regulators in the brain tissue of Alzheimer's disease patients.
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- BMC Medical Genomics, 2018, v. 11, n. 6, p. N.PAG, doi. 10.1186/s12920-018-0431-1
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- Publication type:
- Article
CRlncRNA: a manually curated database of cancer-related long non-coding RNAs with experimental proof of functions on clinicopathological and molecular features.
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- BMC Medical Genomics, 2018, v. 11, n. 6, p. N.PAG, doi. 10.1186/s12920-018-0430-2
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- Article
Novel link prediction for large-scale miRNA-lncRNA interaction network in a bipartite graph.
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- BMC Medical Genomics, 2018, v. 11, n. 6, p. N.PAG, doi. 10.1186/s12920-018-0429-8
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- Publication type:
- Article
Novel disease syndromes unveiled by integrative multiscale network analysis of diseases sharing molecular effectors and comorbidities.
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- BMC Medical Genomics, 2018, v. 11, n. 6, p. N.PAG, doi. 10.1186/s12920-018-0428-9
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- Article
Analytical validation of a prognostic prostate cancer gene expression assay using formalin fixed paraffin embedded tissue.
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- BMC Medical Genomics, 2018, v. 11, n. 1, p. 1, doi. 10.1186/s12920-018-0442-y
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- Publication type:
- Article
Cri-du-chat syndrome mimics Silver-Russell syndrome depending on the size of the deletion: a case report.
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- BMC Medical Genomics, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s12920-018-0441-z
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- Publication type:
- Article
Mapping the landscape of tandem repeat variability by targeted long read single molecule sequencing in familial X-linked intellectual disability.
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- BMC Medical Genomics, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s12920-018-0446-7
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- Publication type:
- Article
A novel PAX5 rearrangement in TCF3-PBX1 acute lymphoblastic leukemia: a case report.
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- BMC Medical Genomics, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s12920-018-0444-9
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- Publication type:
- Article
Genetic investigation into an increased susceptibility to biliary atresia in an extended New Zealand Māori family.
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- BMC Medical Genomics, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s12920-018-0440-0
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- Article
Genomics of lipid-laden human hepatocyte cultures enables drug target screening for the treatment of non-alcoholic fatty liver disease.
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- BMC Medical Genomics, 2018, v. 11, n. 1, p. 1, doi. 10.1186/s12920-018-0438-7
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- Article
"Omics" data integration and functional analyses link Enoyl-CoA hydratase, short chain 1 to drug refractory dilated cardiomyopathy.
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- BMC Medical Genomics, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s12920-018-0439-6
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- Article
Identification of gene expression profiles in myocardial infarction: a systematic review and meta-analysis.
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- BMC Medical Genomics, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s12920-018-0427-x
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- Article
Personal Genome Project UK (PGP-UK): a research and citizen science hybrid project in support of personalized medicine.
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- BMC Medical Genomics, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s12920-018-0423-1
- Publication type:
- Article
Toward the precision breast cancer survival prediction utilizing combined whole genome-wide expression and somatic mutation analysis.
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- BMC Medical Genomics, 2018, v. 11, n. 5, p. N.PAG, doi. 10.1186/s12920-018-0419-x
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- Article
MiteFinderII: a novel tool to identify miniature inverted-repeat transposable elements hidden in eukaryotic genomes.
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- BMC Medical Genomics, 2018, v. 11, n. 5, p. N.PAG, doi. 10.1186/s12920-018-0418-y
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- Article
Discovery and disentanglement of aligned residue associations from aligned pattern clusters to reveal subgroup characteristics.
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- BMC Medical Genomics, 2018, v. 11, n. 5, p. N.PAG, doi. 10.1186/s12920-018-0417-z
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- Publication type:
- Article
Bi-stream CNN Down Syndrome screening model based on genotyping array.
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- BMC Medical Genomics, 2018, v. 11, n. 5, p. N.PAG, doi. 10.1186/s12920-018-0416-0
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- Article
Distributed gene clinical decision support system based on cloud computing.
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- BMC Medical Genomics, 2018, v. 11, n. 5, p. N.PAG, doi. 10.1186/s12920-018-0415-1
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- Publication type:
- Article
Gene Ontology-based function prediction of long non-coding RNAs using bi-random walk.
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- BMC Medical Genomics, 2018, v. 11, n. 5, p. N.PAG, doi. 10.1186/s12920-018-0414-2
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- Publication type:
- Article
Genomic analyses based on pulmonary adenocarcinoma in situ reveal early lung cancer signature.
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- BMC Medical Genomics, 2018, v. 11, n. 5, p. N.PAG, doi. 10.1186/s12920-018-0413-3
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- Article
Human ancestry indentification under resource constraints -- what can one chromosome tell us about human biogeographical ancestry?
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- BMC Medical Genomics, 2018, v. 11, n. 5, p. N.PAG, doi. 10.1186/s12920-018-0412-4
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- Article
Developing a healthcare dataset information resource (DIR) based on Semantic Web.
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- BMC Medical Genomics, 2018, v. 11, n. 5, p. N.PAG, doi. 10.1186/s12920-018-0411-5
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- Publication type:
- Article
integRATE: a desirability-based data integration framework for the prioritization of candidate genes across heterogeneous omics and its application to preterm birth.
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- BMC Medical Genomics, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s12920-018-0426-y
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- Article
A pan-cancer analysis of driver gene mutations, DNA methylation and gene expressions reveals that chromatin remodeling is a major mechanism inducing global changes in cancer epigenomes.
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- BMC Medical Genomics, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s12920-018-0425-z
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- Article
Transposase mapping identifies the genomic targets of BAP1 in uveal melanoma.
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- BMC Medical Genomics, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s12920-018-0424-0
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- Article
Identification of glioblastoma gene prognosis modules based on weighted gene co-expression network analysis.
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- BMC Medical Genomics, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s12920-018-0407-1
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- Article
Nucleotide excision repair is a predictor of early relapse in pediatric acute lymphoblastic leukemia.
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- BMC Medical Genomics, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s12920-018-0422-2
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- Article
Current landscape of personalized medicine adoption and implementation in Southeast Asia.
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- BMC Medical Genomics, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s12920-018-0420-4
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- Article
Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES).
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- BMC Medical Genomics, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s12920-018-0409-z
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- Article
Role of PUF60 gene in Verheij syndrome: a case report of the first Chinese Han patient with a de novo pathogenic variant and review of the literature.
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- 2018
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- Publication type:
- Case Study
Clinical analysis of germline copy number variation in DMD using a non-conjugate hierarchical Bayesian model.
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- BMC Medical Genomics, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s12920-018-0404-4
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- Publication type:
- Article
Strategies to minimize false positives and interpret novel microdeletions based on maternal copy-number variants in 87,000 noninvasive prenatal screens.
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- BMC Medical Genomics, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s12920-018-0410-6
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- Publication type:
- Article
Mitochondrial DNA 7908–8816 region mutations in maternally inherited essential hypertensive subjects in China.
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- BMC Medical Genomics, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s12920-018-0408-0
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- Publication type:
- Article
Logistic regression model training based on the approximate homomorphic encryption.
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- BMC Medical Genomics, 2018, v. 11, n. 4, p. N.PAG, doi. 10.1186/s12920-018-0401-7
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- Article
Privacy-preserving record linkage in large databases using secure multiparty computation.
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- BMC Medical Genomics, 2018, v. 11, n. 4, p. N.PAG, doi. 10.1186/s12920-018-0400-8
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- Publication type:
- Article
Secure top most significant genome variants search: iDASH 2017 competition.
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- BMC Medical Genomics, 2018, v. 11, n. 4, p. N.PAG, doi. 10.1186/s12920-018-0399-x
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- Article
Privacy-preserving logistic regression training.
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- BMC Medical Genomics, 2018, v. 11, n. 4, p. N.PAG, doi. 10.1186/s12920-018-0398-y
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- Article
Logistic regression over encrypted data from fully homomorphic encryption.
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- BMC Medical Genomics, 2018, v. 11, n. 4, p. N.PAG, doi. 10.1186/s12920-018-0397-z
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- Publication type:
- Article
iDASH secure genome analysis competition 2017.
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- BMC Medical Genomics, 2018, v. 11, n. 4, p. N.PAG, doi. 10.1186/s12920-018-0396-0
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- Publication type:
- Article
Genomics of drug sensitivity in bladder cancer: an integrated resource for pharmacogenomic analysis in bladder cancer.
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- BMC Medical Genomics, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s12920-018-0406-2
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- Article
New insights into the phenotypic spectrum of 14q22q23 deletions: a case report and literature review.
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- BMC Medical Genomics, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s12920-018-0405-3
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- Publication type:
- Article
Progression-specific genes identified in microdissected formalin-fixed and paraffin-embedded tissue containing matched ductal carcinoma in situ and invasive ductal breast cancers.
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- BMC Medical Genomics, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s12920-018-0403-5
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- Publication type:
- Article
Local genetic ancestry in CDKN2B-AS1 is associated with primary open-angle glaucoma in an African American cohort extracted from de-identified electronic health records.
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- BMC Medical Genomics, 2018, v. 11, n. 3, p. N.PAG, doi. 10.1186/s12920-018-0392-4
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- Article
Indel sensitive and comprehensive variant/mutation detection from RNA sequencing data for precision medicine.
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- BMC Medical Genomics, 2018, v. 11, n. 3, p. N.PAG, doi. 10.1186/s12920-018-0391-5
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- Publication type:
- Article
Rare variants in the splicing regulatory elements of EXOC3L4 are associated with brain glucose metabolism in Alzheimer’s disease.
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- BMC Medical Genomics, 2018, v. 11, n. 3, p. N.PAG, doi. 10.1186/s12920-018-0390-6
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- Publication type:
- Article