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1.
BMC Genomics ; 17(Suppl 13): 1036, 2016 12 22.
Article in English | MEDLINE | ID: mdl-28155656

ABSTRACT

InCoB became since its inception in 2002 one of the largest annual bioinformatics conferences in the Asia-Pacific region with attendance ranging between 150 and 250 delegates depending on the venue location. InCoB 2016 in Singapore was attended by almost 220 delegates. This year, sessions on structural bioinformatics, sequence and sequencing, and next-generation sequencing fielded the highest number of oral presentation. Forty-four out 96 oral presentations were associated with an accepted manuscript in supplemental issues of BMC Bioinformatics, BMC Genomics, BMC Medical Genomics or BMC Systems Biology. Articles with a genomics focus are reviewed in this editorial. Next year's InCoB will be held in Shenzen, China from September 20 to 22, 2017.


Subject(s)
Computational Biology , Animals , Computational Biology/methods , Genomics/methods , High-Throughput Nucleotide Sequencing , Humans
2.
BMC Genomics ; 17(Suppl 13): 1025, 2016 12 22.
Article in English | MEDLINE | ID: mdl-28155657

ABSTRACT

BACKGROUND: The ability to sequence the transcriptomes of single cells using single-cell RNA-seq sequencing technologies presents a shift in the scientific paradigm where scientists, now, are able to concurrently investigate the complex biology of a heterogeneous population of cells, one at a time. However, till date, there has not been a suitable computational methodology for the analysis of such intricate deluge of data, in particular techniques which will aid the identification of the unique transcriptomic profiles difference between the different cellular subtypes. In this paper, we describe the novel methodology for the analysis of single-cell RNA-seq data, obtained from neocortical cells and neural progenitor cells, using machine learning algorithms (Support Vector machine (SVM) and Random Forest (RF)). RESULTS: Thirty-eight key transcripts were identified, using the SVM-based recursive feature elimination (SVM-RFE) method of feature selection, to best differentiate developing neocortical cells from neural progenitor cells in the SVM and RF classifiers built. Also, these genes possessed a higher discriminative power (enhanced prediction accuracy) as compared commonly used statistical techniques or geneset-based approaches. Further downstream network reconstruction analysis was carried out to unravel hidden general regulatory networks where novel interactions could be further validated in web-lab experimentation and be useful candidates to be targeted for the treatment of neuronal developmental diseases. CONCLUSION: This novel approach reported for is able to identify transcripts, with reported neuronal involvement, which optimally differentiate neocortical cells and neural progenitor cells. It is believed to be extensible and applicable to other single-cell RNA-seq expression profiles like that of the study of the cancer progression and treatment within a highly heterogeneous tumour.


Subject(s)
Brain/metabolism , Gene Expression Profiling , Machine Learning , Organogenesis/genetics , Single-Cell Analysis , Transcriptome , Algorithms , Biomarkers , Brain/embryology , Brain/growth & development , Models, Statistical , Neurogenesis/genetics , Organ Specificity , Reproducibility of Results , Single-Cell Analysis/methods , Support Vector Machine
3.
Front Biosci (Elite Ed) ; 4(1): 311-9, 2012 01 01.
Article in English | MEDLINE | ID: mdl-22201873

ABSTRACT

In the past decade, information technology has enabled synergistic advances in key domains of immunological research including the development of diagnostics and vaccines. Computational methods of epitope mapping now play instrumental roles in bench experiments, by facilitating the selection of immunogenic targets and the modeling of downstream cellular responses. In this article, we summarize the latest development and application of immune epitope prediction methods and discuss future directions in this field which could enhance our understanding of immune specificity.


Subject(s)
Computational Biology , Databases, Protein , Peptides/immunology , Animals , B-Lymphocytes/immunology , Epitopes/immunology , Humans , T-Lymphocytes/immunology
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