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Editions published in BMC Medical Genomics 200
Too many entities requested (1514). Only 200 are displayed.
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Pregnant women carrying microcephaly foetuses and Zika virus contain potentially pathogenic microbes and parasites in their amniotic fluid
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Whole genome sequencing of one complex pedigree illustrates challenges with genomic medicine
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Serum MicroRNA profile in patients with colon adenomas or cancer
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Diet and exercise changes following direct-to-consumer personal genomic testing
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Post-operative atrial fibrillation examined using whole-genome RNA sequencing in human left atrial tissue
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Challenges and strategies for implementing genomic services in diverse settings: experiences from the Implementing GeNomics In pracTicE (IGNITE) network
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CVE: an R package for interactive variant prioritisation in precision oncology.
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Quantitative analysis of cryptic splicing associated with TDP-43 depletion
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Evolution of Translational Bioinformatics: lessons learned from TBC 2016.
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Association analysis of rare variants near the APOE region with CSF and neuroimaging biomarkers of Alzheimer's disease
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Efficient and biologically relevant consensus strategy for Parkinson's disease gene prioritization.
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A comparison of genomic profiles of complex diseases under different models.
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SFRP1 is a possible candidate for epigenetic therapy in non-small cell lung cancer
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Explorations to improve the completeness of exome sequencing
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Unsolved challenges of clinical whole-exome sequencing: a systematic literature review of end-users' views
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Identifying enriched drug fragments as possible candidates for metabolic engineering
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Protecting genomic data analytics in the cloud: state of the art and opportunities
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eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants
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Rules of co-occurring mutations characterize the antigenic evolution of human influenza A/H3N2, A/H1N1 and B viruses
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Genomic approaches to identifying targets for treating β hemoglobinopathies
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Individualized medicine enabled by genomics in Saudi Arabia
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Using gene expression signatures to identify novel treatment strategies in gulf war illness
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Inferring drug-disease associations based on known protein complexes
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TumorTracer: a method to identify the tissue of origin from the somatic mutations of a tumor specimen
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Association of SNPs in LCP1 and CTIF with hearing in 11 year old children: findings from the Avon Longitudinal Study of Parents and Children (ALSPAC) birth cohort and the G-EAR consortium
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Graph pyramids for protein function prediction
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Progression risk assessments of individual non-invasive gastric neoplasms by genomic copy-number profile and mucin phenotype
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Design of a randomized controlled trial of disclosing genomic risk of coronary heart disease: the Myocardial Infarction Genes (MI-GENES) study
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ASEQ: fast allele-specific studies from next-generation sequencing data.
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Relating hepatocellular carcinoma tumor samples and cell lines using gene expression data in translational research
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Identifying network biomarkers based on protein-protein interactions and expression data
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SeedsGraph: an efficient assembler for next-generation sequencing data
Subject - wd:Q15754662