Effects of GC Bias in Next-Generation-Sequencing Data on De Novo Genome Assembly
Open accessAbstract
Next-generation-sequencing (NGS) has revolutionized the field of genome assembly because of its much higher data throughput and much lower cost compared with traditional Sanger sequencing. However, NGS poses new computational challenges to de novo genome assembly. Among the challenges, GC bias in NGS data is known to aggravate genome assembly. However, it is not clear to what extent GC bias affects genome assembly in general. In this work, we conduct a systematic analysis on the effects of GC bias on genome assembly. Our analyses reveal that GC bias only lowers assembly completeness when the degree of GC bias is above a threshold. At a strong GC bias, the assembly fragmentation due to GC bias can be explained by the low coverage of reads in the GC-poor or GC-rich regions of a genome. This effect is observed for all the assemblers under study. Increasing the total amount of NGS data thus rescues the assembly fragmentation because of GC bias. However, the amount of data needed for a full rescue depends on the distribution of GC contents. Both low and high coverage depths due to GC bias lower the accuracy of assembly. These pieces of information provide guidance toward a better de novo genome assembly in the presence of GC bias.
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High-throughput sequencing and sample dilution are modeled using random sampling because GC content in the files did not show practically significant bias in the PCR GC bias test.
“Illumina sequencing was previously observed to have bias on GC-extreme sequences15,27,28, but GC content in our files did not show practically significant bias in the PCR GC bias test. Therefore, high-throughput sequencing and sample dilution are modeled using random sampling.”
From Quantifying Molecular Bias in DNA Data Storage (2019) · cites this paper as [27]
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Database resources of the National Center for Biotechnology Information: update
Wheeler, D. L. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkh073 · Cited by 10,691 · see citing works
Velvet: Algorithms for de novo short read assembly using de Bruijn graphsPreprint
Zerbino, D. R., & Birney, E. (2008) · Genome Research · doi:10.1101/gr.074492.107 · Cited by 9,387 · see citing works
Genome sequencing in microfabricated high-density picolitre reactors
Margulies, M., Egholm, M., Altman, W. E., Attiya, S., Bader, J. S., Bemben, L. A., Berka, J., Braverman, M. S., Chen, Y.-J., Chen, Z., et al. (2005) · Nature · doi:10.1038/nature03959 · Cited by 7,693 · see citing works
Self-citationSequencing technologies – the next generation
Metzker, M. L. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2626 · Cited by 7,066 · see citing works
Versatile and open software for comparing large genomes
Kurtz, S., Phillippy, A., Delcher, A. L., Smoot, M., Shumway, M., Antonescu, C., & Salzberg, S. L. (2004) · Genome Biology · doi:10.1186/gb-2004-5-2-r12 · Cited by 5,254 · see citing works
Accurate whole human genome sequencing using reversible terminator chemistry
Bentley, D. R., Balasubramanian, S., Swerdlow, H. P., Smith, G. P., Milton, J., Brown, C. G., Hall, K. P., Evers, D. J., Barnes, C. L., Bignell, H. R., et al. (2008) · Nature · doi:10.1038/nature07517 · Cited by 3,684 · see citing works
ABySS: A parallel assembler for short read sequence dataPreprint
Simpson, J. T., Wong, K., Jackman, S. D., Schein, J. E., Jones, S. J. M., & Birol, İ. (2009) · Genome Research · doi:10.1101/gr.089532.108 · Cited by 3,583 · see citing works
De novo assembly of human genomes with massively parallel short read sequencing
Li, R., Zhu, H., Ruan, J., Qian, W., Fang, X., Shi, Z., Li, Y., Li, S., Shan, G., Kristiansen, K., et al. (2010) · Genome Research · doi:10.1101/gr.097261.109 · Cited by 2,926 · cited 1× · see citing works
“In this study, we applied seven NGS assemblers: ALLPATHS-LG [24,25], ABySS [26], Edena [27], SOAPdenovo [28], SSAKE [29], Velvet [30,31] and Velvet-SC [14].”
MethodBias caused by template annealing in the amplification of mixtures of 16S rRNA genes by PCR
Suzuki, M. T., & Giovannoni, S. (1996) · Applied and Environmental Microbiology · doi:10.1128/aem.62.2.625-630.1996 · Cited by 2,021 · see citing works
Next-generation sequencing transforms today's biology
Schuster, S. C. (2007) · Nature Methods · doi:10.1038/nmeth1156 · Cited by 1,813 · see citing works
Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries
Aird, D., Ross, M. G., Chen, W.-S., Danielsson, M., Fennell, T., Russ, C., Jaffe, D. B., Nusbaum, C., & Gnirke, A. (2011) · Genome Biology · doi:10.1186/gb-2011-12-2-r18 · Cited by 1,174 · see citing works
Substantial biases in ultra-short read data sets from high-throughput DNA sequencing
Dohm, J. C., Lottaz, C., Borodina, T., & Himmelbauer, H. (2008) · Nucleic Acids Research · doi:10.1093/nar/gkn425 · Cited by 1,088 · see citing works
Pagani, I., Liolios, K., Jansson, J., Chen, I.-M. A., Smirnova, T., Nosrat, B., Markowitz, V. M., & Kyrpides, N. C. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr1100 · Cited by 1,061 · see citing works
Summarizing and correcting the GC content bias in high-throughput sequencing
Benjamini, Y., & Speed, T. P. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks001 · Cited by 913 · see citing works
ALLPATHS: de novo assembly of whole-genome shotgun microreads.Preprint
Butler, J., Maccallum, I., Kleber, M., Shlyakhter, I., Belmonte, M., Lander, E., Nusbaum, C., & Jaffe, D. (2008) · Genome Research · doi:10.1101/gr.7337908 · Cited by 893 · see citing works
A large genome center's improvements to the Illumina sequencing system
Quail, M. A., Kozarewa, I., Smith, F., Scally, A., Stephens, P. J., Durbin, R. M., Swerdlow, H., & Turner, D. (2008) · Nature Methods · doi:10.1038/nmeth.1270 · Cited by 732 · see citing works
PILER: identification and classification of genomic repeats
Edgar, R. C., & Myers, E. W. (2005) · Bioinformatics · doi:10.1093/bioinformatics/bti1003 · Cited by 711 · see citing works
Fisher, S., Barry, A. J., Abreu, J., Minie, B., Nolan, J., Delorey, T. M., Young, G., Fennell, T. J., Allen, A., Ambrogio, L., et al. (2011) · Genome biology · doi:10.1186/gb-2011-12-1-r1 · Cited by 683 · see citing works
GAGE: A critical evaluation of genome assemblies and assembly algorithmsPreprint
Salzberg, S. L., Phillippy, A. M., Zimin, A. V., Puiu, D., Magoč, T., Koren, S., Treangen, T. J., Schatz, M. C., Delcher, A. L., Roberts, M., et al. (2011) · Genome Research · doi:10.1101/gr.131383.111 · Cited by 680 · see citing works
Optimizing illumina next-generation sequencing library preparation for extremely at-biased genomes
Oyola, S. O., Otto, T. D., Gu, Y., Maslen, G. L., Manske, M., Campino, S. G., Turner, D., MacInnis, B. L., Kwiatkowski, D. P., Swerdlow, H., et al. (2012) · BMC Genomics · doi:10.1186/1471-2164-13-1 · Cited by 654 · see citing works
Kozarewa, I., Ning, Z., Quail, M. A., Sanders, M. J., Berriman, M., & Turner, D. J. (2009) · Nature Methods · doi:10.1038/nmeth.1311 · Cited by 565 · see citing works
Database resources of the National Center for Biotechnology Information
Sayers, E. W., Barrett, T., Benson, D. A., Bolton, E., Bryant, S. H., Canese, K., Chetvernin, V., Church, D. M., DiCuccio, M. N., Federhen, S., et al. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr1184 · Cited by 524 · see citing works
Assembling millions of short DNA sequences using SSAKE
Warren, R. M., Sutton, G. G., Jones, S. J. M., & Holt, R. A. (2006) · Bioinformatics · doi:10.1093/bioinformatics/btl629 · Cited by 497 · see citing works
Whole-genome sequencing and variant discovery in C. elegans
Hillier, L. W., Marth, G., Quinlan, A. R., Dooling, D. J., Fewell, G. A., Barnett, D. W., Fox, P. M., Glasscock, J. I., Hickenbotham, M. T., Huang, W., et al. (2008) · Nature Methods · doi:10.1038/nmeth.1179 · Cited by 405 · see citing works
Genome assembly reborn: recent computational challenges
Pop, M. (2009) · Briefings in Bioinformatics · doi:10.1093/bib/bbp026 · Cited by 382 · see citing works
Rapid whole-genome mutational profiling using next-generation sequencing technologiesPreprint
Smith, D. R., Quinlan, A. R., Peckham, H. E., Makowsky, K., Tao, W., Woolf, B., Shen, L., Donahue, W. F., Tusneem, N. A., Strömberg, M. P., et al. (2008) · Genome Research · doi:10.1101/gr.077776.108 · Cited by 260 · see citing works
Zhang, W., Chen, J., Yang, Y., Tang, Y., Shang, J., & Shen, B. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017915 · Cited by 250 · see citing works
Efficient de novo assembly of single-cell bacterial genomes from short-read data sets
Chitsaz, H., Yee-Greenbaum, J. L., Tesler, G., Lombardo, M., Dupont, C. L., Badger, J. H., Novotny, M. A., Rusch, D. B., Fraser, L. J., Gormley, N. A., et al. (2011) · Nature Biotechnology · doi:10.1038/nbt.1966 · Cited by 236 · see citing works
Comparative analysis of algorithms for next-generation sequencing read alignment
Ruffalo, M., LaFramboise, T., & Koyutürk, M. (2011) · Bioinformatics · doi:10.1093/bioinformatics/btr477 · Cited by 232 · see citing works
Zerbino, D. R., McEwen, G. K., Margulies, E. H., & Birney, E. (2009) · PLoS ONE · doi:10.1371/journal.pone.0008407 · Cited by 224 · see citing works
An efficient and economic enhancer mix for PCR
Ralser, M., Querfurth, R., Warnatz, H.-J., Lehrach, H. R., Yaspo, M., & Krobitsch, S. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.06.151 · Cited by 213 · see citing works
De novo assembly of short sequence reads
Paszkiewicz, K., & Studholme, D. J. (2010) · Briefings in Bioinformatics · doi:10.1093/bib/bbq020 · Cited by 204 · see citing works
ALLPATHS 2: small genomes assembled accurately and with high continuity from short paired reads
MacCallum, I., Przybylski, D., Gnerre, S., Burton, J. N., Shlyakhter, I. A., Gnirke, A., Malek, J. A., McKernan, K. J., Ranade, S., Shea, T., et al. (2009) · Genome biology · doi:10.1186/gb-2009-10-10-r103 · Cited by 180 · see citing works
Challenges of sequencing human genomes
Koboldt, D., Ding, L., Mardis, E., & Wilson, R. K. (2010) · Briefings Bioinform. · doi:10.1093/bib/bbq016 · Cited by 158 · see citing works
Comparing De Novo Genome Assembly: The Long and Short of It
Narzisi, G., & Mishra, B. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019175 · Cited by 146 · see citing works
Amplification efficiency of thermostable DNA polymerases
Arezi, B., Xing, W., Sorge, J. A., & Hogrefe, H. H. (2003) · Analytical Biochemistry · doi:10.1016/s0003-2697(03)00465-2 · Cited by 144 · see citing works
A fundamental study of the PCR amplification of GC-rich DNA templates
Mamedov, T., Pienaar, E., Whitney, S. E., TerMaat, J. R., Carvill, G. L., Goliath, R., Subramanian, A., & Viljoen, H. J. (2008) · Computational Biology and Chemistry · doi:10.1016/j.compbiolchem.2008.07.021 · Cited by 128 · see citing works
Comparative studies of <i>de novo</i> assembly tools for next-generation sequencing technologies
Lin, Y., Li, J., Shen, H., Zhang, L., Papasian, C. J., & Deng, H. (2011) · Bioinformatics · doi:10.1093/bioinformatics/btr319 · Cited by 126 · see citing works
Improved PCR Method for Amplification of GC-Rich DNA Sequences
Hubé, F., Reverdiau, P., Iochmann, S., & Gruel, Y. (2005) · Molecular Biotechnology · doi:10.1385/mb:31:1:081 · Cited by 67 · see citing works
Sequencing and Genome Assembly Using Next-Generation Technologies
Nagarajan, N., & Pop, M. (2010) · Methods in molecular biology · doi:10.1007/978-1-60761-842-3_1 · Cited by 53 · see citing works
A fast hybrid short read fragment assembly algorithm
Schmidt, B., Sinha, R., Beresford‐Smith, B., & Puglisi, S. J. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp374 · Cited by 53 · see citing works
Golovko, G., Khanipov, K., Rojas, M., Martinez-Alcántara, A., Howard, J. J., Ballesteros, E., Gupta, S., Widger, W. R., & Fofanov, Y. (2012) · BMC Bioinformatics · doi:10.1186/1471-2105-13-166 · Cited by 10 · see citing works
Shintani, M., Matsumoto, T., Yoshikawa, H., Yamane, H., Ohkuma, M., Nojiri, H., & Top, E. M. (2011) · Microbiology · doi:10.1099/mic.0.053280-0 · Cited by 10 · see citing works
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Delahaye, C., & Nicolas, J. (2021) · PLoS ONE · doi:10.1371/journal.pone.0257521 · Cited by 529 · see citing works
Primer and platform effects on 16S rRNA tag sequencing
Tremblay, J., Singh, K. P., Fern, A., Kirton, E., He, S., Woyke, T., Lee, J., Chen, F., Dangl, J. L., & Tringe, S. G. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.00771 · Cited by 530 · see citing works
KrakenUniq: confident and fast metagenomics classification using unique k-mer counts
Breitwieser, F. P., Baker, D. N., & Salzberg, S. L. (2018) · Genome biology · doi:10.1186/s13059-018-1568-0 · Cited by 480 · see citing works
Gillieatt, B. F., & Coleman, N. V. (2024) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuae017 · Cited by 293 · see citing works
Angly, F. E., Dennis, P. G., Skarshewski, A., Vanwonterghem, I., Hugenholtz, P., & Tyson, G. W. (2014) · Microbiome · doi:10.1186/2049-2618-2-11 · Cited by 293 · see citing works
Reevaluating the Genetic Contribution of Monogenic Dilated Cardiomyopathy
Mazzarotto, F., Tayal, U., Buchan, R. J., Midwinter, W., Wilk, A., Whiffin, N., Govind, R., Mazaika, E., de Marvao, A., Dawes, T. J. W., et al. (2020) · Circulation · doi:10.1161/circulationaha.119.037661 · Cited by 259 · see citing works
Analysis of plant microbe interactions in the era of next generation sequencing technologies
Knief, C. (2014) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00216 · Cited by 252 · see citing works
From Benchtop to Desktop: Important Considerations when Designing Amplicon Sequencing Workflows
Murray, D. C., Coghlan, M. L., & Bunce, M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0124671 · Cited by 222 · see citing works
The present and future ofde novowhole-genome assembly
Sohn, J.-I., & Nam, J. (2016) · Briefings in Bioinformatics · doi:10.1093/bib/bbw096 · Cited by 198 · see citing works
HEDGES error-correcting code for DNA storage corrects indels and allows sequence constraints
Press, W. H., Hawkins, J. A., Jones, S. K., Schaub, J. M., & Finkelstein, I. J. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2004821117 · Cited by 178 · see citing works
GC bias affects genomic and metagenomic reconstructions, underrepresenting GC-poor organisms
Browne, P. D., Nielsen, T. K., Kot, W., Aggerholm, A., Gilbert, M. T. P., Puetz, L., Rasmussen, M., Zervas, A., & Hansen, L. H. (2020) · GigaScience · doi:10.1093/gigascience/giaa008 · Cited by 175 · see citing works
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Berná, L., Rodriguez, M., Chiribao, M. L., Parodi‐Talice, A., Pita, S., Rijo, G., Álvarez-Valín, F., & Robello, C. (2018) · Microbial Genomics · doi:10.1099/mgen.0.000177 · Cited by 166 · see citing works
Pflug, J. M., Holmes, V. R., Burrus, C., Johnston, J. S., & Maddison, D. R. (2020) · G3 Genes Genomes Genetics · doi:10.1534/g3.120.401028 · Cited by 157 · see citing works
Goldstein, S., Beka, L., Graf, J., & Klassen, J. L. (2019) · BMC Genomics · doi:10.1186/s12864-018-5381-7 · Cited by 154 · see citing works
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Yang, G., Chen, Y., Wang, J., Guo, C., Zhao, L., Wang, X., Guo, Y. Q., Li, L., Li, D.-Z., & Guo, Z. (2016) · Plant Methods · doi:10.1186/s13007-016-0139-1 · Cited by 96 · see citing works
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Gene loss, adaptive evolution and the co-evolution of plumage coloration genes with opsins in birds
Borges, R., Khan, I., Johnson, W. E., Gilbert, M. T. P., Zhang, G., Jarvis, E. D., O’Brien, S. J., & Antunes, A. (2015) · BMC Genomics · doi:10.1186/s12864-015-1924-3 · Cited by 65 · see citing works
Yuan, X., Bai, J., Zhang, J., Yang, L., Duan, J., Li, Y., & Gao, M. (2018) · IEEE Transactions on Computational Biology and Bioinformatics · doi:10.1109/tcbb.2018.2883333 · Cited by 59 · see citing works
Tyler, A. D., Christianson, S., Knox, N., Mabon, P., Wolfe, J. N., Domselaar, G. V., Graham, M., & Sharma, M. K. (2016) · PLoS ONE · doi:10.1371/journal.pone.0148676 · Cited by 59 · see citing works
Koumbaris, G., Kypri, E., Tsangaras, K., Achilleos, A., Mina, P., Neofytou, M. C., Velissariou, V., Christopoulou, G., Kallikas, I., González-Liñán, A., et al. (2016) · Clinical Chemistry · doi:10.1373/clinchem.2015.252502 · Cited by 53 · see citing works
IntSIM: An Integrated Simulator of Next-Generation Sequencing Data
Yuan, X., Zhang, J., & Yang, L. (2016) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2016.2560939 · Cited by 52 · see citing works
Mood and hormonal changes during late pregnancy and puerperium.
Asher, I., Kaplan, B., Modai, I., Neri, A., Valevski, A., & Weizman, A. (1995) · PubMed · Cited by 51 · see citing works
Heitkam, T., Weber, B., Walter, I., Liedtke, S., Ost, C., & Schmidt, T. (2020) · The Plant Journal · doi:10.1111/tpj.14705 · Cited by 50 · see citing works
Fourth Report on Chicken Genes and Chromosomes 2022
Smith, J., Alfieri, J. M., Anthony, N., Arensburger, P., Athrey, G., Balacco, J., Balic, A., Bardou, P., Barela, P., Bigot, Y., et al. (2022) · Cytogenetic and Genome Research · doi:10.1159/000529376 · Cited by 52 · see citing works
Vasudevan, K., Ragupathi, N. K. D., Jacob, J. J., & Veeraraghavan, B. (2019) · Genomics · doi:10.1016/j.ygeno.2019.04.006 · Cited by 49 · see citing works
Chiocchetti, A. G., Kopp, M., Waltes, R., Haslinger, D., Duketis, E., Jarczok, T. A., Poustka, F., Voran, A., Graab, U., Meyer, J., et al. (2014) · Molecular Psychiatry · doi:10.1038/mp.2014.103 · Cited by 47 · see citing works
Morales‐Hojas, R., Hinsley, M., Armean, I. M., Silk, R. N., Harrup, L. E., Gonzalez‐Uriarte, A., Veronesi, E., Campbell, L. I., Nayduch, D., Saski, C. A., et al. (2018) · BMC Genomics · doi:10.1186/s12864-018-5014-1 · Cited by 47 · see citing works
Egan, C., Rummel, A., Kokkoris, V., Klironomos, J. N., Lekberg, Y., & Hart, M. M. (2018) · Fungal ecology · doi:10.1016/j.funeco.2018.01.004 · Cited by 45 · see citing works
Kiefer, J. S. T., Batsukh, S., Bauer, E., Hirota, B., Weiß, B., Wierz, J. C., Fukatsu, T., Kaltenpoth, M., & Engl, T. (2021) · Communications Biology · doi:10.1038/s42003-021-02057-6 · Cited by 43 · see citing works
Luan, X., Liu, D., Cao, Z., Luo, L., Liu, M., Gao, M., & Zhang, X. (2014) · PLoS ONE · doi:10.1371/journal.pone.0113211 · Cited by 43 · see citing works
Martínez-Álvaro, M., Mattock, J., Auffret, M. D., Weng, Z., Duthie, C.-A., Dewhurst, R. J., Cleveland, M. A., Watson, M., & Roehe, R. (2022) · Microbiome · doi:10.1186/s40168-022-01352-6 · Cited by 41 · see citing works
Next-Generation Sequencing in Diagnostic Pathology
Ilyas, M. (2017) · Pathobiology · doi:10.1159/000480089 · Cited by 42 · see citing works
Hloušková, P., Mandáková, T. M., Pouch, M., Trávníček, P., & Lysák, M. A. (2019) · Annals of Botany · doi:10.1093/aob/mcz036 · Cited by 41 · see citing works
Firdaus, Z., & Li, X. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25042320 · Cited by 43 · see citing works
GABenchToB: A Genome Assembly Benchmark Tuned on Bacteria and Benchtop Sequencers
Jünemann, S., Prior, K., Albersmeier, A., Albaum, S. P., Kalinowski, J., Goesmann, A., Stoye, J., & Harmsen, D. (2014) · PLoS ONE · doi:10.1371/journal.pone.0107014 · Cited by 39 · see citing works
Neofytou, M. C., Tsangaras, K., Kypri, E., Loizides, C., Ioannides, M., Achilleos, A., Mina, P., Keravnou, A., Sismani, C., Koumbaris, G., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0171319 · Cited by 39 · see citing works
Hargreaves, A. D., Zhou, L., Christensen, J., Marlétaz, F., Liu, S., Li, F., Jansen, P. G., Spiga, E., Hansen, M. T., Pedersen, S. V. H., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1702930114 · Cited by 38 · see citing works
A method for achieving complete microbial genomes and improving bins from metagenomics data
Lui, L., Nielsen, T., & Arkin, A. (2020) · bioRxiv · doi:10.1371/journal.pcbi.1008972 · Cited by 37 · see citing works
Variable Spontaneous Mutation and Loss of Heterozygosity among Heterozygous Genomes in Yeast
Nguyen, D. T., Wu, B., Long, H., Zhang, N., Patterson, C. E., Simpson, S., Morris, K., Thomas, W. K., Lynch, M., & Hao, W. (2020) · Molecular Biology and Evolution · doi:10.1093/molbev/msaa150 · Cited by 37 · see citing works
SNP in the Coffea arabica genome associated with coffee quality
Tran, H. T. M., Furtado, A., Vargas, C. A., Smyth, H. E., Lee, L. S., & Henry, R. J. (2018) · Tree Genetics & Genomes · doi:10.1007/s11295-018-1282-9 · Cited by 37 · see citing works
Resequencing Helminth Genomes for Population and Genetic Studies
Wit, J., & Gilleard, J. S. (2017) · Trends in Parasitology · doi:10.1016/j.pt.2017.01.009 · Cited by 36 · see citing works
Regional sequence expansion or collapse in heterozygous genome assemblies
Asalone, K. C., Ryan, K., Yamadi, M., Cohen, A., Farmer, W. G., George, D. J., Joppert, C., Kim, K., Mughal, M. F., Said, R., et al. (2020) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1008104 · Cited by 36 · see citing works
Chung, S. H., Mollhoff, I. N., Nguyen, U. T. T., Nguyen, A. B., Stucka, N., Tieu, E., Manna, S. K., Meleppat, R. K., Zhang, P., Nguyen, E. L., et al. (2020) · Molecular Therapy — Methods & Clinical Development · doi:10.1016/j.omtm.2020.01.006 · Cited by 35 · see citing works
Saski, C. A., Bhattacharjee, R., Scheffler, B. E., & Asiedu, R. (2015) · PLoS ONE · doi:10.1371/journal.pone.0134031 · Cited by 34 · see citing works
Applying Genome-Resolved Metagenomics to Deconvolute the Halophilic Microbiome
Uritskiy, G., & DiRuggiero, J. (2019) · Genes · doi:10.3390/genes10030220 · Cited by 33 · see citing works
Integrated next-generation sequencing analysis of whole exome and 409 cancer-related genes
Shimoda, Y., Nagashima, T., Urakami, K., TANABE, T., SAITO, J., Naruoka, A., Serizawa, M., Mochizuki, T., Ohshima, K., Ohnami, S., et al. (2016) · Biomedical Research · doi:10.2220/biomedres.37.367 · Cited by 32 · see citing works
RUBICON: a framework for designing efficient deep learning-based genomic basecallers
Singh, G., Alser, M., Denolf, K., Fırtına, C., Khodamoradi, A., Cavlak, M. B., Corporaal, H., & Mutlu, O. (2024) · Genome biology · doi:10.1186/s13059-024-03181-2 · Cited by 31 · see citing works
Zhao, Z., Wu, G., Wang, J., Liu, C., & Qiu, L.-H. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080146 · Cited by 30 · see citing works
Yao, Y., Nishimura, M., Murayama, K., Kuranobu, N., Tojo-Nishimura, S., Beppu, M., Ishige, T., Itoga, S., Tsuchida, S., Mori, M., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-53449-y · Cited by 30 · see citing works
Salavati, M., Caulton, A., Clark, R. C., Gažová, I., Smith, T. P. L., Worley, K. C., Cockett, N. E., Archibald, A. L., Clarke, S., Murdoch, B. M., et al. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2020.580580 · Cited by 29 · see citing works
Haplotype-aware inference of human chromosome abnormalities
Ariad, D., Yan, S. M., Victor, A. R., Barnes, F. L., Zouves, C., Viotti, M., & McCoy, R. C. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2109307118 · Cited by 29 · see citing works
Neuronal microRNA regulation in Experimental Autoimmune Encephalomyelitis
Juźwik, C. A., Drake, S. S., Lécuyer, M.-A., Johnson, R. M., Morquette, B., Zhang, Y., Charabati, M., Sagan, S., Bar-Or, A., Prat, A., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-31542-y · Cited by 29 · see citing works
A deep learning framework for imputing missing values in genomic dataPreprint
Qiu, Y. L., Zheng, H., & Gevaert, O. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/406066 · Cited by 29 · see citing works
Prevention, diagnosis and treatment of high‐throughput sequencing data pathologies
Zhou, X., & Rokas, A. (2014) · Molecular Ecology · doi:10.1111/mec.12680 · Cited by 29 · see citing works
Yuan, X., Zhang, J., Yang, L., Bai, J., & Fan, P. (2017) · IEEE Transactions on NanoBioscience · doi:10.1109/tnb.2017.2783910 · Cited by 28 · see citing works
Kim, M., Park, S., Baek, I., & Chun, J. (2014) · Systematic and Applied Microbiology · doi:10.1016/j.syapm.2014.11.008 · Cited by 27 · see citing works
Zseq: An Approach for Preprocessing Next-Generation Sequencing Data
Alkhateeb, A., & Rueda, L. G. (2017) · Journal of Computational Biology · doi:10.1089/cmb.2017.0021 · Cited by 27 · see citing works
Investigation into the annotation of protocol sequencing steps in the sequence read archive
Alnasir, J. J., & Shanahan, H. P. (2015) · GigaScience · doi:10.1186/s13742-015-0064-7 · Cited by 27 · see citing works
Contribution of Next-Generation Sequencing to Aquatic and Fish Virology
Nkili-Meyong, A. A., Bigarré, L., Labouba, I., Vallaeys, T., Avarre, J., & Berthet, N. (2016) · Intervirology · doi:10.1159/000477808 · Cited by 27 · see citing works
The microbiome of common bedding materials before and after use on commercial dairy farms
Ray, T., Gaire, T. N., Dean, C., Rowe, S. M., Godden, S., & Noyes, N. R. (2022) · Animal Microbiome · doi:10.1186/s42523-022-00171-2 · Cited by 25 · see citing works
Baets, S. D., Verhelst, J., den Hoecke, S. V., Smet, A., Schotsaert, M., Job, E. R., Roose, K., Schepens, B., Fiers, W. C., & Saelens, X. (2015) · PLoS ONE · doi:10.1371/journal.pone.0121491 · Cited by 25 · see citing works
Developing and characterising Ricinus communis SSR markers by data mining of whole-genome sequences
Tan, M., Wu, K., Wang, L., Yan, M., Zhao, Z., Xu, J., Zeng, Y., Zhang, X., Fu, C., Xue, J., et al. (2014) · Molecular Breeding · doi:10.1007/s11032-014-0083-6 · Cited by 25 · see citing works
TIGER: inferring DNA replication timing from whole-genome sequence data
Koren, A., Massey, D. J., & Bracci, A. N. (2021) · Bioinformatics · doi:10.1093/bioinformatics/btab166 · Cited by 24 · see citing works
In vitro and in silico parameters for precise cgMLST typing of Listeria monocytogenes
Palma, F., Mangone, I., Janowicz, A., Moura, A., Chiaverini, A., Torresi, M., Garofolo, G., Criscuolo, A., Brisse, S., Pasquale, A. D., et al. (2022) · BMC Genomics · doi:10.1186/s12864-022-08437-4 · Cited by 22 · see citing works
Revisiting Rustrela Virus: New Cases of Encephalitis and a Solution to the Capsid Enigma
Pfaff, F., Breithaupt, A., Rubbenstroth, D., Nippert, S., Baumbach, C., Gerst, S., Langner, C., Wylezich, C., Ebinger, A., Höper, D. W., et al. (2022) · Microbiology Spectrum · doi:10.1128/spectrum.00103-22 · Cited by 22 · see citing works
A practical comparison of the next-generation sequencing platform and assemblers using yeast genome
Jeon, M., Jeong, D. M., Doh, H., Kang, H. A., Jung, H., & Eyun, S. (2023) · Life Science Alliance · doi:10.26508/lsa.202201744 · Cited by 21 · see citing works
Evaluating coverage bias in next-generation sequencing of Escherichia coli
Gunasekera, S., Abraham, S., Stegger, M., Pang, S., Wang, P., Sahibzada, S., & O’Dea, M. A. (2021) · PLoS ONE · doi:10.1371/journal.pone.0253440 · Cited by 19 · see citing works
Evaluation of a high-throughput, cost-effective Illumina library preparation kit
Tvedte, E. S., Michalski, J. M., Cheng, S., Patkus, R. S., Tallon, L. J., Sadzewicz, L., Bruno, V. M., da Silva, J. C. F., Rasko, D. A., & Hotopp, J. C. D. (2021) · Scientific Reports · doi:10.1038/s41598-021-94911-0 · Cited by 18 · see citing works
Choi, I., Wojciechowski, M. F., Steele, K. P., Hopkins, A., Ruhlman, T. A., & Jansen, R. K. (2022) · Scientific Reports · doi:10.1038/s41598-022-25381-1 · Cited by 19 · see citing works
Marr, R. A., Moore, J., Formby, S., Martiniuk, J. T., Hamilton, J., Ralli, S., Konwar, K. M., Rajasundaram, N., Hahn, A. S., & Measday, V. (2023) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkad130 · Cited by 19 · see citing works
MetaGen: reference-free learning with multiple metagenomic samples
Xing, X., Liu, J. S., & Zhong, W. (2017) · Genome biology · doi:10.1186/s13059-017-1323-y · Cited by 19 · see citing works
Wu, B., Li, M., Liao, X., Luo, J., Wu, F., Pan, Y. F., & Wang, J. (2018) · IEEE Transactions on Computational Biology and Bioinformatics · doi:10.1109/tcbb.2018.2876855 · Cited by 19 · see citing works
- Authors
- Chen, Y.-C., Liu, T., Yu, C.-H., Chiang, T.-Y., & Hwang, C.-C.
- Affiliations
- National Cheng Kung University (TW)
- Corresponding author
- Hwang, Chi-Chuan
- Venue
- PLoS ONE
- Publisher
- Public Library of Science (PLoS)
- Published
- 2013-04-29
- Volume
- 8
- Issue
- 4
- Pages
- e62856
- ISSN
- 1932-6203 (ISSN-L)
- PMC
- PMC3639258
- OpenAlex
- W1998330439
- Cited by
- 285
- References
- 43
- Citations by year
- 2026: 7 · 2025: 22 · 2024: 25 · 2023: 20 · 2022: 26 · 2021: 48 · 2020: 30 · 2019: 13 · 2018: 27 · 2017: 23 · 2016: 18 · 2015: 11 · 2014: 12 · 2013: 2
- FWCI
- 6.42
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- PLoS ONE (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, other-oa)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Figshare (submittedVersion, cc-by)
- Funders
- National Science Council
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Physical Sciences › Computer Science › Artificial Intelligence › Algorithms and Data Compression
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fractal and DNA sequence analysis
- Keywords
- GC content bias, de novo genome assembly, next-generation sequencing, assembly completeness, read coverage, assembly accuracy
- MeSH terms
- Reference Standards, Artifacts, Genome, Bacterial, GC Rich Sequence, Genomics, High-Throughput Nucleotide Sequencing
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