TY - JOUR
T1 - An adaptive landscape for training in the essentials of next gen sequencing data acquisition and bioinformatic analysis
AU - Farman, Mark
AU - Calie, Patrick
AU - Jaromczyk, Jerzy
AU - Jaromczyk, Jolanta
AU - Moore, Neil
AU - Harris, Daniel
AU - Schardl, Chris
N1 - Publisher Copyright:
© Farman et al; licensee BioMed Central Ltd.
PY - 2014/9/29
Y1 - 2014/9/29
N2 - Background Recent technological advances in Next Generation Sequencing (NGS) have reduced both the cost and time required to produce Large Data Sets (LDS) of nucleotide sequences. These advances have led to an exponential proliferation of nucleotide sequence data coupled with an exacerbation of a persistent conundrum: the level of difficulty in generating LDS is rapidly decreasing, but the exposure, development and training of students and investigators in the bioinformatic approaches requisite to the proper and correct analysis of such data sets is experiencing a parallel increase in difficulty. Materials and methods To address this national need, we have developed a clientoriented Summer Workshop in NGS technology and related bioinformatics that combines a practical experience to the biological and technical aspects of NGS coupled with an integrated bioinformatic exposure to a suite of appropriate analytical tools and approaches. The biological component utilizes experiences in both semiconductor and sequencing by synthesis technologies with nucleic acid samples provided to the Workshop clients. This allows clients to understand issues of DNA quality, biological sample contamination, and preliminary quality assessment of the output data. The bioinformatic modules then use the client-generated data as working platforms to allow the clients to engage in such activities as assessing sequence quality, de novo genome assembly, alignment of RNASeq data to a reference genome, construction of in silico gene models, and populating a genome browser, to name a few. The global perspective of the workshop is to develop client skills in formulating appropriate scientific questions prior to investing in NGS approaches, in choosing the most appropriate NGS platform (pyrosequencing, semi-conductor sequencing, or sequencing by synthesis) suitable for their specific questions, and in the efficient and correct analysis of genomic and transcriptomic data sets. In this, our third year, we continue to modify and adapt the Workshop curriculum to address the evolving needs of our clients, based upon our experiences with real time data from our Advanced Genetic Technologies Center at the University of Kentucky. One anticipated outcome is the future development of a virtual community of former and current Workshop participants who can share experiences and insights as NGS technologies and allied bioinformatic approaches evolve through time.
AB - Background Recent technological advances in Next Generation Sequencing (NGS) have reduced both the cost and time required to produce Large Data Sets (LDS) of nucleotide sequences. These advances have led to an exponential proliferation of nucleotide sequence data coupled with an exacerbation of a persistent conundrum: the level of difficulty in generating LDS is rapidly decreasing, but the exposure, development and training of students and investigators in the bioinformatic approaches requisite to the proper and correct analysis of such data sets is experiencing a parallel increase in difficulty. Materials and methods To address this national need, we have developed a clientoriented Summer Workshop in NGS technology and related bioinformatics that combines a practical experience to the biological and technical aspects of NGS coupled with an integrated bioinformatic exposure to a suite of appropriate analytical tools and approaches. The biological component utilizes experiences in both semiconductor and sequencing by synthesis technologies with nucleic acid samples provided to the Workshop clients. This allows clients to understand issues of DNA quality, biological sample contamination, and preliminary quality assessment of the output data. The bioinformatic modules then use the client-generated data as working platforms to allow the clients to engage in such activities as assessing sequence quality, de novo genome assembly, alignment of RNASeq data to a reference genome, construction of in silico gene models, and populating a genome browser, to name a few. The global perspective of the workshop is to develop client skills in formulating appropriate scientific questions prior to investing in NGS approaches, in choosing the most appropriate NGS platform (pyrosequencing, semi-conductor sequencing, or sequencing by synthesis) suitable for their specific questions, and in the efficient and correct analysis of genomic and transcriptomic data sets. In this, our third year, we continue to modify and adapt the Workshop curriculum to address the evolving needs of our clients, based upon our experiences with real time data from our Advanced Genetic Technologies Center at the University of Kentucky. One anticipated outcome is the future development of a virtual community of former and current Workshop participants who can share experiences and insights as NGS technologies and allied bioinformatic approaches evolve through time.
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U2 - 10.1186/1471-2105-15-S10-P25
DO - 10.1186/1471-2105-15-S10-P25
M3 - Article
AN - SCOPUS:84961647336
SN - 1471-2105
VL - 15
JO - BMC Bioinformatics
JF - BMC Bioinformatics
IS - 10
M1 - P25
ER -