Data Analysis of Multiplex Sequencing at SOLiD Platform: A Probabilistic Approach to Characterization and Reliability Increase
- 1 Engineering and Geoscience Institute, Federal University of Western Pará (UFOPa), Santarém, Brazil
- 2 Institute of Mathematical and Computer Sciences, University of São Paulo (USP), São Carlos, Brazil
- 3 Department of Morphology and Physiological Sciences, State University of Pará, Marabá, Brazil
- 4 Biological Science Institute, Federal University of Pará (UFPa), Belém, Brazil
- 5 Biological Science Institute, Federal University of Pará (UFPa), Belém, Brazil
- 6 Technological Institute, Federal University of Pará (UFPa), Belém, Brazil
- 7 Laboratory of Computing and Applied Mathematics, National Institute for Space Research (INPE), São José Dos Campos, Brazil
- 8 Technological Institute, Federal University of Pará (UFPa), Belém, Brazil
Abstract
New sequencing technologies such as Illumina/Solexa, SOLiD/ABI, and 454/Roche, revolutionized the biological researches. In this context, the SOLiD platform has a particular sequencing type, known as multiplex run, which enables the sequencing of several samples in a single run. It implies in cost reduction and simplifies the analysis of related samples. Meanwhile, this sequencing type requires an additional filtering step to ensure the reliability of the results. Thus, we propose in this paper a probabilistic model which considers the intrinsic characteristics of each sequencing to characterize multiplex runs and filter low-quality data, increasing the data analysis reliability of multiplex sequencing performed on SOLiD. The results show that the proposed model proves to be satisfactory due to: 1) identification of faults in the sequencing process; 2) adaptation and development of new protocols for sample preparation; 3) the assignment of a degree of confidence to the data generated; and 4) guiding a filtering process, without discarding useful sequences in an arbitrary manner.
- Ma, R., Gong, J. and Jiang, X. (2017) Novel Applications of Next-Generation Sequencing in Breast Cancer Research. Genes & Diseases, 4, 149-153. https://doi.org/10.1016/j.gendis.2017.07.003
- Mardis, E.R. (2013) Next-Generation Sequencing Platforms. Annual Review of Analytical Chemistry, 6, 287-303. https://doi.org/10.1146/annurev-anchem-062012-092628
- Dopazo, J. (2014) Genomics and Transcriptomics in Drug Discovery. Drug Discovery Today, 19, 126-132. https://doi.org/10.1016/j.drudis.2013.06.003
- Pillai, S., Gopalan, V. and Lam, A.K.-Y. (2017) Review of Sequencing Platforms and Their Applications in Phaeochromocytoma and Paragangliomas. Critical Reviews in Oncology/Hematology, 116 (Supplement C), 58-67. https://doi.org/10.1016/j.critrevonc.2017.05.005
- David, M., Dzamba, M., Lister, D., Ilie, L. and Brudno, M. (2011) Shrimp2: Sensitive Yet Practical Short Read Mapping. Bioinformatics, 27, 1011-1012. https://doi.org/10.1093/bioinformatics/btr046
- Li, H. and Homer, N. (2010) A Survey of Sequence Alignment Algorithms for Next-Generation Sequencing. Briefings in Bioinformatics, 11, 473-483. https://doi.org/10.1093/bib/bbq015
- Applied Biosystem, SOL-iD(TM) System Barcoding, Application Note (2008).
- Applied Biosystem, SOLiD(TM) Fragment Library Barcoding Kit Module 1{16 Protocol, Tech. rep., Thermo Fisher Scientific Inc. (2010)
- Ambardar, S., Gupta, R., Trakroo, D., Lal, R. and Vakhlu, J. (2016) High Throughput Sequencing: An Overview of Sequencing Chemistry. Indian Journal of Microbiology, 56, 394-404. https://doi.org/10.1007/s12088-016-0606-4
- Parameswaran, P., Jalili, R., Tao, L., Shokralla, S., Gharizadeh, B., Ronaghi, M. and Fire, A.Z. (2007) A Pyrosequencing-Tailored Nucleotide Barcode Design Unveils Opportunities for Large-Scale Sample Multiplexing. Nucleic Acids Research, 35, e130. https://doi.org/10.1093/nar/gkm760
- Farrer, R.A., Henk, D.A., MacLean, D., Studholme, D.J. and Fisher, M.C. (2013) Using False Discovery Rates to Benchmark SNP-Callers in Next-Generation Sequencing Projects. Scientific Reports, 3, 1512.
- Parker, D.J., Ritchie, M.G. and Kankare, M. (2016) Preparing for Winter: The Transcriptomic Response Associated with Different Day Lengths in Drosophila Montana. G3: Genes, Genomes, Genetics, 6, 1373-1381.
- Richardson, R., Mitchell, K., Hammond, N.L., Mollo, M.R., Kouwenhoven, E.N., Wyatt, N.D., Donaldson, I.J., Zeef, L., Burgis, T., Blance, R., van Heeringen, S.J., Stunnenberg, H.G., Zhou, H., Missero, C., Romano, R.A., Sinha, S., Dixon, M.J. and Dixon, J. (2017) p63 Exerts Spatio-Temporal Control of Palatal Epithelial Cell Fate to Prevent Cleft Palate. PLOS Genetics, 13, 1-24. https://doi.org/10.1371/journal.pgen.1006828