van Dijk, E. L., Auger, H., Jaszczyszyn, Y. and Thermes, C. (2014) Ten years of next-generation sequencing technology. Trends Genet., 30, 418–426
Article
PubMed
Google Scholar
Metzker, M. L. (2010) Sequencing technologies— the next generation. Nat. Rev. Genet., 11, 31–46
CAS
Article
PubMed
Google Scholar
Shendure, J. and Ji, H. (2008) Next-generation DNA sequencing. Nat. Biotechnol., 26, 1135–1145
CAS
Article
PubMed
Google Scholar
Schlötterer, C., Tobler, R., Kofler, Rand Nolte, V. (2014) Sequencing pools of individuals—mining genome-wide polymorphism data without big funding. Nat. Rev. Genet., 15, 749–763
Article
PubMed
Google Scholar
Futschik, A. and Schlötterer, C. (2010) The next generation of molecular markers from massively parallel sequencing of pooled DNA samples. Genetics, 186, 207–218
CAS
Article
PubMed
PubMed Central
Google Scholar
Patterson, N. and Gabriel, S. (2009) Combinatorics and next-generation sequencing. Nat. Biotechnol., 27, 826–827
CAS
Article
PubMed
Google Scholar
Wang, W., Yin, X., Soo Pyon, Y., Hayes, Mand Li, J. (2013) Rare variant discovery and calling by sequencing pooled samples with overlaps. Bioinformatics, 29, 29–38
Article
PubMed
PubMed Central
Google Scholar
Smith, A. M., Heisler, L. E., St Onge, R. P., Farias-Hesson, E.,Wallace, I. M., Bodeau, J., Harris, A. N., Perry, K. M., Giaever, G., Pourmand, N., et al. (2010) Highly-multiplexed barcode sequencing: an efficient method for parallel analysis of pooled samples. Nucleic Acids Res., 38, e142
Article
PubMed
PubMed Central
Google Scholar
Gautier, M., Foucaud, J., Gharbi, K., Cézard, T., Galan, M., Loiseau, A., Thomson, M., Pudlo, P., Kerdelhué, C. and Estoup, A. (2013) Estimation of population allele frequencies from next-generation sequencing data: pool-versus individual-based genotyping. Mol. Ecol., 22, 3766–3779
CAS
Article
PubMed
Google Scholar
Cao, C.-C. and Sun, X. (2015) Accurate estimation of haplotype frequency from pooled sequencing data and cost-effective identification of rare haplotype carriers by overlapping pool sequencing. Bioinformatics, 31, 515–522
Article
PubMed
Google Scholar
Lonardi, S., Duma, D., Alpert, M., Cordero, F., Beccuti, M., Bhat, P. R., Wu, Y., Ciardo, G., Alsaihati, B., Ma, Y., et al. (2013) Combinatorial pooling enables selective sequencing of the barley gene space. PLoS Comput. Biol., 9, e1003010
CAS
Article
PubMed
PubMed Central
Google Scholar
Lo, C., Liu, R., Lee, J., Robasky, K., Byrne, S., Lucchesi, C., Aach, J., Church, G., Bafna, V. and Zhang, K. (2013) On the design of clonebased haplotyping. Genome Biol., 14, R100
Article
PubMed
PubMed Central
Google Scholar
Skums, P., Artyomenko, A., Glebova, O., Ramachandran, S., Mandoiu, I., Campo, D. S., Dimitrova, Z., Zelikovsky, A. and Khudyakov, Y. (2015) Computational framework for next-generation sequencing of heterogeneous viral populations using combinatorial pooling. Bioinformatics, 31, 682–690
Article
PubMed
Google Scholar
Ngo, H., and Du, D. (2000) A survey on combinatorial group testing algorithms with applications to DNA library screening. Discrete mathematical problems with medical applications, 55, 171–182.
Google Scholar
Erlich, Y., Chang, K., Gordon, A., Ronen, R., Navon, O., Rooks, M. and Hannon, G. J. (2009) DNA Sudoku—harnessing high-throughput sequencing for multiplexed specimen analysis. Genome Res., 19, 1243–1253
CAS
Article
PubMed
PubMed Central
Google Scholar
Thierry-Mieg, N. (2006) A new pooling strategy for high-throughput screening: the Shifted Transversal Design. BMC Bioinformatics, 7, 28
Article
PubMed
PubMed Central
Google Scholar
Dorfman, R. (1943) The detection of defective members of large populations. Ann. Math. Stat., 14, 436–440.
Article
Google Scholar
Prabhu, S. and Pe’er, I. (2009) Overlapping pools for high-throughput targeted resequencing. Genome Res., 19, 1254–1261
CAS
Article
PubMed
PubMed Central
Google Scholar
Chen, H.-B. and Hwang, F. K. (2008) A survey on nonadaptive group testing algorithms through the angle of decoding. J. Comb. Optim., 15, 49–59.
CAS
Article
Google Scholar
Candes, E., Romberg, J. and Tao, T. (2006) Stable signal recovery from incomplete and inaccurate measurements. Commun. Pure Appl. Math., 59, 1207–1223.
Article
Google Scholar
Donoho, D. (2006) Compressed sensing. IEEE Trans. Inf. Theory, 52, 1289–1306.
Article
Google Scholar
Bodmer, W. and Bonilla, C. (2008) Common and rare variants in multifactorial susceptibility to common diseases. Nat. Genet., 40, 695–701
CAS
Article
PubMed
PubMed Central
Google Scholar
Manolio, T. A., Collins, F. S., Cox, N. J., Goldstein, D. B., Hindorff, L. A., Hunter, D. J., McCarthy, M. I., Ramos, E. M., Cardon, L. R., Chakravarti, A., et al. (2009) Finding the missing heritability of complex diseases. Nature, 461, 747–753
CAS
Article
PubMed
PubMed Central
Google Scholar
Nelson, M. R., Wegmann, D., Ehm, M. G., Kessner, D., St Jean, P., Verzilli, C., Shen, J., Tang, Z., Bacanu, S. A., Fraser, D., et al. (2012) An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people. Science, 337, 100–104
CAS
Article
PubMed
PubMed Central
Google Scholar
Tennessen, J. A., Bigham, A. W., O’Connor, T. D., Fu, W., Kenny, E. E., Gravel, S., McGee, S., Do, R., Liu, X., Jun, G., et al., (2012) Evolution and functional impact of rare coding variation from deep sequencing of human exomes. Science, 337, 64–69
CAS
Article
PubMed
PubMed Central
Google Scholar
Du, D. and Hwang, F. (2000) Combinatorial group testing and its applications, 2nd ed. Singapore: World Scientific
Thierry-Mieg, N. and Bailly, G. (2008) Interpool: interpreting smartpooling results. Bioinformatics, 24, 696–703
CAS
Article
PubMed
Google Scholar
Golan, D., Erlich, Y. and Rosset, S. (2012) Weighted pooling—practical and cost-effective techniques for pooled high-throughput sequencing. Bioinformatics, 28, i197–i206
CAS
Article
PubMed
PubMed Central
Google Scholar
Shental, N., Amir, A. and Zuk, O. (2010) Identification of rare alleles and their carriers using compressed se(que)nsing. Nucleic Acids Res., 38, e179
Article
PubMed
PubMed Central
Google Scholar
Erlich, Y., Gordon, A., Brand, M., Hannon, G. J. and Mitra, P. P. (2010) Compressed Genotyping. IEEE Trans. Inf. Theory, 56, 706–723
Article
PubMed
PubMed Central
Google Scholar
Erlich, Y., Shental, N., Amir, A. and Zuk, O. (2009) Compressed sensing approach for high throughput carrier screen. In Communication, Control, and Computing, 2009 Allerton 2009 47th Annual Allerton Conference
Google Scholar
Figueiredo, M. A., Nowak, R. D., and Wright, S. J. (2007) Gradient projection for sparse reconstruction: Application to compressed sensing and other inverse problems. Selected Topics in Signal Processing, 1, 586–597
Article
Google Scholar
Cao, C.-C., Li, C. and Sun, X. (2014) Quantitative group testing-based overlapping pool sequencing to identify rare variant carriers. BMC Bioinformatics, 15, 195
Article
PubMed
PubMed Central
Google Scholar
Hwang, F. (2000) Random k-set pool designs with distinct columns. Probab. Engrg. Inform. Sci., 14, 49–56.
Article
Google Scholar
He, D., Zaitlen, N., Pasaniuc, B., Eskin, E. and Halperin, E. (2011) Genotyping common and rare variation using overlapping pool sequencing. BMC Bioinformatics, 12, S2
Google Scholar
Hormozdiariy, F., Wang, Z., Yangy, W. -Y. and Eskiny, E. (2012) Efficient genotyping of individuals using overlapping pool sequencing and imputation. In Signals, Systems and Computers (ASILOMAR), 2012 Conference Record of the Forty Sixth Asilomar Conference. 1023–1027.
Chapter
Google Scholar
Zuzarte, P. C., Denroche, R. E., Fehringer, G., Katzov-Eckert, H., Hung, R. J. and McPherson, J. D. (2014) A two-dimensional pooling strategy for rare variant detection on next-generation sequencing platforms. PLoS One, 9, e93455
Article
PubMed
PubMed Central
Google Scholar
Bonachea, E. M., Zender, G., White, P., Corsmeier, D., Newsom, D., Fitzgerald-Butt, S., Garg, V. and McBride, K. L. (2014) Use of a targeted, combinatorial next-generation sequencing approach for the study of bicuspid aortic valve. BMC Med. Genomics, 7, 56
Article
PubMed
PubMed Central
Google Scholar
Cao, C.-C., Li, C., Huang, Z., Ma, X. and Sun, X. (2013) Identifying rare variants with optimal depth of coverage and cost-effective overlapping pool sequencing. Genet. Epidemiol., 37, 820–830
Article
PubMed
Google Scholar
Trégouët, D.-A., König, I. R., Erdmann, J., Munteanu, A., Braund, P. S., Hall, A. S., Grosshennig, A., Linsel-Nitschke, P., Perret, C., DeSuremain, M., et al. (2009) Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease. Nat. Genet., 41, 283–285
Article
PubMed
Google Scholar
Niu, T. (2004) Algorithms for inferring haplotypes. Genet. Epidemiol., 27, 334–347
Article
PubMed
Google Scholar
Iliadis, A., Anastassiou, D. and Wang, X. (2012) Fast and accurate haplotype frequency estimation for large haplotype vectors from pooled DNA data. BMC Genet., 13, 94
CAS
Article
PubMed
PubMed Central
Google Scholar
Chang, Y.-C., Chang, L.-Y., Chang, T.-J., Jiang, Y.-D., Lee, K.-C., Kuo, S.-S., Lee, W.-J. and Chuang, L.-M. (2010) The associations of LPIN1 gene expression in adipose tissue with metabolic phenotypes in the Chinese population. Obesity (Silver Spring), 18, 7–12
CAS
Article
Google Scholar
Jin, H., Stewart, T. L., Hof, R. V., Reid, D. M., Aspden, R. M. and Ralston, S. (2009) A rare haplotype in the upstream regulatory region of COL1A1 is associated with reduced bone quality and hip fracture. J. Bone Miner. Res., 24, 448–454
CAS
Article
PubMed
Google Scholar
Lambert, J. C., Grenier-Boley, B., Harold, D., Zelenika, D., Chouraki, V., Kamatani, Y., Sleegers, K., Ikram, M. A., Hiltunen, M., Reitz, C., et al. (2013) Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer’s disease. Mol. Psychiatry, 18, 461–470
CAS
Article
PubMed
PubMed Central
Google Scholar
Martin, R. J. L., McKnight, A. J., Patterson, C. C., Sadlier, D. M., Maxwell, A. P. and Group, T. W. U. G. S., and the Warren 3/UK GoKinD Study Group. (2010) A rare haplotype of the vitamin D receptor gene is protective against diabetic nephropathy. Nephrol. Dial. Transplant., 25, 497–503
CAS
Article
PubMed
Google Scholar
Long, Q., Jeffares, D. C., Zhang, Q., Ye, K., Nizhynska, V., Ning, Z., Tyler-Smith, C. and Nordborg, M. (2011) PoolHap: inferring haplotype frequencies from pooled samples by next generation sequencing. PLoS One, 6, e15292
CAS
Article
PubMed
PubMed Central
Google Scholar
Kessner, D., Turner, T. L. and Novembre, J. (2013) Maximum likelihood estimation of frequencies of known haplotypes from pooled sequence data. Mol. Biol. Evol., 30, 1145–1158
CAS
Article
PubMed
PubMed Central
Google Scholar
Pirinen, M. (2009) Estimating population haplotype frequencies from pooled SNP data using incomplete database information. Bioinformatics, 25, 3296–3302
CAS
Article
PubMed
Google Scholar
Gasbarra, D., Kulathinal, S., Pirinen, M. and Sillanpää, M. J. (2011) Estimating haplotype frequencies by combining data from large DNA pools with database information. IEEE/ACM Trans. Comput. Biol. Bioinformatics, 8, 36–44
Article
Google Scholar
Treangen, T. J. and Salzberg, S. L. (2012) Repetitive DNA and nextgeneration sequencing: computational challenges and solutions. Nat. Rev. Genet., 13, 36–46
CAS
Google Scholar
Zhang, G., Fang, X., Guo, X., Li, L., Luo, R., Xu, F., Yang, P., Zhang, L., Wang, X., Qi, H., et al. (2012) The oyster genome reveals stress adaptation and complexity of shell formation. Nature, 490, 49–54
CAS
Article
PubMed
Google Scholar
Lonardi, S., Duma, D., Alpert, M., Cordero, F., Beccuti, M., Bhat, P. R., Wu, Y., Ciardo, G., Alsaihati, B. and Ma, Y. (2011) Barcoding-free BAC pooling enables combinatorial selective sequencing of the barley gene space. arXiv:1112.4438.
Google Scholar
Engler, F. W., Hatfield, J., Nelson, W. and Soderlund, C. A. (2003) Locating sequence on FPC maps and selecting a minimal tiling path. Genome Res., 13, 2152–2163
CAS
Article
PubMed
PubMed Central
Google Scholar
Bozdag, S., Close, T. J. and Lonardi, S. (2008) Computing the minimal tiling path from a physical map by integer linear programming. In Algorithms in Bioinformatics. 148–161. Berlin: Springer Berlin Heidelberg
Chapter
Google Scholar
Duma, D., Wootters, M., Gilbert, A. C., Ngo, H. Q., Rudra, A., Alpert, M., Close, T. J., Ciardo, G. and Lonardi, S. (2013) Accurate decoding of pooled sequenced data using compressed sensing. In Algorithms in Bioinformatics. 70–84. Berlin: Springer Berlin Heidelberg
Chapter
Google Scholar
Glusman, G., Cox, H. Cand Roach, J. C. (2014) Whole-genome haplotyping approaches and genomic medicine. Genome Med., 6, 73
Article
PubMed
PubMed Central
Google Scholar
Yang, H., Chen, X. and Wong, W. H. (2011) Completely phased genome sequencing through chromosome sorting. Proc. Natl. Acad. Sci. USA, 108, 12–17
CAS
Article
PubMed
PubMed Central
Google Scholar
Fan, H. C., Wang, J., Potanina, A. and Quake, S. R. (2011) Wholegenome molecular haplotyping of single cells. Nat. Biotechnol., 29, 51–57
CAS
Article
PubMed
PubMed Central
Google Scholar
Ma, L., Xiao, Y., Huang, H., Wang, Q., Rao, W., Feng, Y., Zhang, K. and Song, Q. (2010) Direct determination of molecular haplotypes by chromosome microdissection. Nat. Methods, 7, 299–301
CAS
Article
PubMed
PubMed Central
Google Scholar
Selvaraj, S., R Dixon, J., Bansal, Vand Ren, B. (2013) Whole-genome haplotype reconstruction using proximity-ligation and shotgun sequencing. Nat. Biotechnol., 31, 1111–1118
CAS
Article
PubMed
PubMed Central
Google Scholar
Snyder, M. W., Adey, A., Kitzman, J. O. and Shendure, J. (2015) Haplotype-resolved genome sequencing: experimental methods and applications. Nat. Rev. Genet., 16, 344–358
CAS
Article
PubMed
Google Scholar
Kitzman, J. O., Mackenzie, A. P., Adey, A., Hiatt, J. B., Patwardhan, R. P., Sudmant, P. H., Ng, S. B., Alkan, C., Qiu, R., Eichler, E. E., et al. (2011) Haplotype-resolved genome sequencing of a Gujarati Indian individual. Nat. Biotechnol., 29, 59–63
CAS
Article
PubMed
PubMed Central
Google Scholar
Suk, E.-K., McEwen, G. K., Duitama, J., Nowick, K., Schulz, S., Palczewski, S., Schreiber, S., Holloway, D. T., McLaughlin, S., Peckham, H., et al. (2011) A comprehensively molecular haplotyperesolved genome of a European individual. Genome Res., 21, 1672–1685
CAS
Article
PubMed
PubMed Central
Google Scholar
Peters, B. A., Kermani, B. G., Sparks, A. B., Alferov, O., Hong, P., Alexeev, A., Jiang, Y., Dahl, F., Tang, Y. T., Haas, J., et al. (2012) Accurate whole-genome sequencing and haplotyping from 10 to 20 human cells. Nature, 487, 190–195
CAS
Article
PubMed
PubMed Central
Google Scholar
Kaper, F., Swamy, S., Klotzle, B., Munchel, S., Cottrell, J., Bibikova, M., Chuang, H.-Y., Kruglyak, S., Ronaghi, M., Eberle, M. A., et al. (2013) Whole-genome haplotyping by dilution, amplification, and sequencing. Proc. Natl. Acad. Sci. USA, 110, 5552–5557
CAS
Article
PubMed
PubMed Central
Google Scholar
Amini, S., Pushkarev, D., Christiansen, L., Kostem, E., Royce, T., Turk, C., Pignatelli, N., Adey, A., Kitzman, J. O., Vijayan, K., et al. (2014) Haplotype-resolved whole-genome sequencing by contiguity-preserving transposition and combinatorial indexing. Nat. Genet., 46, 1343–1349
CAS
Article
PubMed
PubMed Central
Google Scholar
Zielinski, D., Gordon, A., Zaks, B. L. and Erlich, Y. (2014) iPipet: sample handling using a tablet. Nat. Methods, 11, 784–785
CAS
Article
PubMed
Google Scholar
Cradic, K.W., Murphy, S. J., Drucker, T. M., Sikkink, R. A., Eberhardt, N. L., Neuhauser, C., Vasmatzis, G. and Grebe, S. K. (2014) A simple method for gene phasing using mate pair sequencing. BMC Med. Genet., 15, 19
Article
PubMed
PubMed Central
Google Scholar
Feder, A. F., Petrov, D. A. and Bergland, A. O. (2012) LDx: estimation of linkage disequilibrium from high-throughput pooled resequencing data. PLoS One, 7, e48588
CAS
Article
PubMed
PubMed Central
Google Scholar
Clarke, J., Wu, H. C., Jayasinghe, L., Patel, A., Reid, S. and Bayley, H. (2009) Continuous base identification for single-molecule nanopore DNA sequencing. Nat. Nanotechnol., 4, 265–270
CAS
Article
PubMed
Google Scholar
Eid, J., Fehr, A., Gray, J., Luong, K., Lyle, J., Otto, G., Peluso, P., Rank, D., Baybayan, P., Bettman, B., et al. (2009) Real-time DNA sequencing from single polymerase molecules. Science, 323, 133–138
CAS
Article
PubMed
Google Scholar
Konczal, M., Koteja, P., Stuglik, M. T., Radwan, J. and Babik, W. (2014) Accuracy of allele frequency estimation using pooled RNA-Seq. Mol. Ecol. Resour., 14, 381–392
CAS
Article
PubMed
Google Scholar
Hill, J. T., Demarest, B. L., Bisgrove, B. W., Gorsi, B., Su, Y. -C., and Yost, H. J. (2013) MMAPPR: mutation mapping analysis pipeline for pooled RNA-seq. Genome Res., 23, 687–697.
CAS
Article
PubMed
PubMed Central
Google Scholar