Volume 14 Supplement 1
Edited by Cenk Sahinalp and Steven Jones
Publication of this supplement was funded by the authors.
The Eleventh Asia Pacific Bioinformatics Conference (APBC 2013). Go to conference site.
Vancouver, Canada
21-24 January 2013
Proceedings
Genome-wide association studies (GWAS) have identified many common polymorphisms associated with complex traits. However, these associated common variants explain only a small fraction of the phenotypic varian...
BMC Genomics 2013 14(Suppl 1):S1
Published on: 21 January 2013
Proceedings
MicroRNAs (miRNAs) play a critical role in down-regulating gene expression. By coupling with Argonaute family proteins, miRNAs bind to target sites on mRNAs and employ translational repression. A large amount ...
BMC Genomics 2013 14(Suppl 1):S2
Published on: 21 January 2013
Proceedings
Pairwise comparison of time series data for both local and time-lagged relationships is a computationally challenging problem relevant to many fields of inquiry. The Local Similarity Analysis (LSA) statistic i...
BMC Genomics 2013 14(Suppl 1):S3
Published on: 21 January 2013
Proceedings
Deciphering cis-regulatory networks has become an attractive yet challenging task. This paper presents a simple method for cis-regulatory network discovery which aims to avoid some of the common problems of previ...
BMC Genomics 2013 14(Suppl 1):S4
Published on: 21 January 2013
Proceedings
Glycine max is an economically important crop and many different varieties of soybean exist around the world. The first draft sequences and gene models of G. max (domesticated soybean) as well as G. soja (wild so...
BMC Genomics 2013 14(Suppl 1):S5
Published on: 21 January 2013
Proceedings
Yeast deletion-mutant collections have been successfully used to infer the mode-of-action of drugs especially by profiling chemical-genetic and genetic-genetic interactions on a genome-wide scale. Although ten...
BMC Genomics 2013 14(Suppl 1):S6
Published on: 21 January 2013
Proceedings
Error correction of sequenced reads remains a difficult task, especially in single-cell sequencing projects with extremely non-uniform coverage. While existing error correction tools designed for standard (mul...
BMC Genomics 2013 14(Suppl 1):S7
Published on: 21 January 2013
Proceedings
Recent studies in genomics have highlighted the significance of structural variation in determining individual variation. Current methods for identifying structural variation, however, are predominantly focuse...
BMC Genomics 2013 14(Suppl 1):S8
Published on: 21 January 2013
Proceedings
The cost of RNA-Seq has been decreasing over the last few years. Despite this, experiments with four or less biological replicates are still quite common. Estimating the variances of gene expression estimates ...
BMC Genomics 2013 14(Suppl 1):S9
Published on: 21 January 2013
Proceedings
Reconstructability of population history, from genetic information of extant individuals, is studied under a simulation setting. We do not address the issue of accuracy of the reconstruction algorithms: we ass...
BMC Genomics 2013 14(Suppl 1):S10
Published on: 21 January 2013
Proceedings
Identifying the genetic variants that contribute to disease susceptibilities is important both for developing methodologies and for studying complex diseases in molecular biology. It has been demonstrated that...
BMC Genomics 2013 14(Suppl 1):S11
Published on: 21 January 2013
Proceedings
Structural variations in human genomes, such as deletions, play an important role in cancer development. Next-Generation Sequencing technologies have been central in providing ways to detect such variations. M...
BMC Genomics 2013 14(Suppl 1):S12
Published on: 21 January 2013
The Erratum to this article has been published in BMC Genomics 2013 14:S16
Proceedings
With the introduction of next-generation sequencing (NGS) technologies, we are facing an exponential increase in the amount of genomic sequence data. The success of all medical and genetic applications of next...
BMC Genomics 2013 14(Suppl 1):S13
Published on: 21 January 2013
Proceedings
One challenge in applying bioinformatic tools to clinical or biological data is high number of features that might be provided to the learning algorithm without any prior knowledge on which ones should be used...
BMC Genomics 2013 14(Suppl 1):S14
Published on: 21 January 2013
Proceedings
Gene duplication, followed by functional evolution of duplicate genes, is a primary engine of evolutionary innovation. In turn, gene expression evolution is a critical component of overall functional evolution...
BMC Genomics 2013 14(Suppl 1):S15
Published on: 21 January 2013
Erratum
BMC Genomics 2013 14(Suppl 1):S16
Published on: 15 March 2013
The original article was published in BMC Genomics 2013 14:S12
The editors of BMC Genomics support initiatives that expedite the peer review process and are happy to consider manuscripts that have been reviewed in Peerage of Science. Please indicate in your cover letter if this applies to your manuscript.
