Volume 13 Supplement 1
Publication of this supplement has not been supported by sponsorship. Information about the source of funding for publication charges can be found in the individual articles. The articles have undergone the journal's standard peer review process for supplements. The Supplement Editor declares no competing interests.
Madrid, Spain3-6 December 2018
Edited by Illhoi Yoo.
MicroRNAs (miRNAs) are a family of short, non-coding RNAs that have been linked to critical cellular activities, most notably regulation of gene expression. The identification of miRNA is a cross-disciplinary ...
Citation: Human Genomics 2019 13(Suppl 1):43
As one of the most popular data representation methods, non-negative matrix decomposition (NMF) has been widely concerned in the tasks of clustering and feature selection. However, most of the previously propo...
Citation: Human Genomics 2019 13(Suppl 1):46
Protein–protein interaction (PPI) information extraction from biomedical literature helps unveil the molecular mechanisms of biological processes. Especially, the PPIs associated with human malignant neoplasms...
Citation: Human Genomics 2019 13(Suppl 1):44
Microbes are greatly associated with human health and disease, especially in densely populated cities. It is essential to understand the microbial ecosystem in an urban environment for cities to monitor the tr...
Citation: Human Genomics 2019 13(Suppl 1):47
In recent years, with the development of high-throughput genome sequencing technologies, a large amount of genome data has been generated, which has caused widespread concern about data storage and transmissio...
Citation: Human Genomics 2019 13(Suppl 1):49
Gene set analysis is a well-established approach for interpretation of data from high-throughput gene expression studies. Achieving reproducible results is an essential requirement in such studies. One factor ...
Citation: Human Genomics 2019 13(Suppl 1):42
De novo genome assembly is a technique that builds the genome of a specimen using overlaps of genomic fragments without additional work with reference sequence. Sequence fragments (called reads) are assembled ...
Citation: Human Genomics 2019 13(Suppl 1):48
Modern applications such as bioinformatics collecting data in various ways can easily result in heterogeneous data. Traditional variable selection methods assume samples are independent and identically distrib...
Citation: Human Genomics 2019 13(Suppl 1):45
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0.885 - Source Normalized Impact per Paper (SNIP)
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Human Genomics
