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Volume 19 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 that they have no competing interests.
Seoul, Korea31 October - 3 November 2017
Edited by Jin-Wu Nam.
Related articles have been published in supplements to BMC Systems Biology and BMC Medical Genomics.
Aberrant mutations in KRAS play a critical role in tumor initiation and progression, and are a negative prognosis factor in lung adenocarcinoma (LUAD).
Citation: BMC Bioinformatics 2018 19(Suppl 1):40
Published on: 19 February 2018
The haplotype assembly problem for diploid is to find a pair of haplotypes from a given set of aligned Single Nucleotide Polymorphism (SNP) fragments (reads). It has many applications in association studies, d...
Citation: BMC Bioinformatics 2018 19(Suppl 1):52
Published on: 19 February 2018
LncRNAs are long regulatory non-coding RNAs, some of which are arguably predicted to have coding potential. Despite coding potential classifiers that utilize ribosome profiling data successfully detected activ...
Citation: BMC Bioinformatics 2018 19(Suppl 1):41
Published on: 19 February 2018
The read length of single-molecule DNA sequencers is reaching 1 Mb. Popular alignment software tools widely used for analyzing such long reads often take advantage of single-instruction multiple-data (SIMD) op...
Citation: BMC Bioinformatics 2018 19(Suppl 1):45
Published on: 19 February 2018
DNA damage causes aging, cancer, and other serious diseases. The comet assay can detect multiple types of DNA lesions with high sensitivity, and it has been widely applied. Although comet assay platforms have ...
Citation: BMC Bioinformatics 2018 19(Suppl 1):44
Published on: 19 February 2018
The Correction to this article has been published in BMC Bioinformatics 2018 19:170
Bioinformatics research for finding biological mechanisms can be done by analysis of transcriptome data with pathway based interpretation. Therefore, researchers have tried to develop tools to analyze transcri...
Citation: BMC Bioinformatics 2018 19(Suppl 1):42
Published on: 19 February 2018
Since many proteins become functional only after they interact with their partner proteins and form protein complexes, it is essential to identify the sets of proteins that form complexes. Therefore, several c...
Citation: BMC Bioinformatics 2018 19(Suppl 1):39
Published on: 19 February 2018
It is known that functional RNAs often switch their functions by forming different secondary structures. Popular tools for RNA secondary structures prediction, however, predict the single ‘best’ structures, an...
Citation: BMC Bioinformatics 2018 19(Suppl 1):38
Published on: 19 February 2018
While next-generation sequencing (NGS) costs have fallen in recent years, the cost and complexity of computation remain substantial obstacles to the use of NGS in bio-medical care and genomic research. The rap...
Citation: BMC Bioinformatics 2018 19(Suppl 1):43
Published on: 19 February 2018
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