메뉴 건너뛰기




Volumn 16, Issue 1, 2015, Pages

ViVaMBC: Estimating viral sequence variation in complex populations from illumina deep-sequencing data using model-based clustering

Author keywords

Codon; Illumina sequencing; Model based clustering; Second best base call; Viral quasispecies

Indexed keywords

ERRORS; NUCLEOTIDES; PROBABILITY; QUALITY CONTROL; VIRUSES;

EID: 84928225279     PISSN: None     EISSN: 14712105     Source Type: Journal    
DOI: 10.1186/s12859-015-0458-7     Document Type: Article
Times cited : (11)

References (31)
  • 1
    • 52649157765 scopus 로고    scopus 로고
    • Substantial biases in ultra-short read data sets from high-throughput dna sequencing
    • Dohm JC, Lottaz C, Borodina T, Himmelbauer H. Substantial biases in ultra-short read data sets from high-throughput dna sequencing. Nucleic Acids Res. 2008; 36(16):105.
    • (2008) Nucleic Acids Res. , vol.36 , Issue.16 , pp. 105
    • Dohm, J.C.1    Lottaz, C.2    Borodina, T.3    Himmelbauer, H.4
  • 2
    • 84874964797 scopus 로고    scopus 로고
    • Challenges and opportunities in estimating viral genetic diversity from next-generation sequencing data
    • Beerenwinkel N, Günthard HF, Roth V, Metzner KJ. Challenges and opportunities in estimating viral genetic diversity from next-generation sequencing data. Front Microbiol. 2012; 3:329.
    • (2012) Front Microbiol. , vol.3 , pp. 329
    • Beerenwinkel, N.1    Günthard, H.F.2    Roth, V.3    Metzner, K.J.4
  • 4
    • 77950840976 scopus 로고    scopus 로고
    • Deep sequencing of a genetically heterogeneous sample: local haplotype reconstruction and read error correction
    • Zagordi O, Geyrhofer L, Roth V, Beerenwinkel N. Deep sequencing of a genetically heterogeneous sample: local haplotype reconstruction and read error correction. J Comput Biol. 2010; 17(3):417-28.
    • (2010) J Comput Biol. , vol.17 , Issue.3 , pp. 417-428
    • Zagordi, O.1    Geyrhofer, L.2    Roth, V.3    Beerenwinkel, N.4
  • 5
    • 79955125679 scopus 로고    scopus 로고
    • Shorah: estimating the genetic diversity of a mixed sample from next-generation sequencing data
    • Zagordi O, Bhattacharya A, Eriksson N, Beerenwinkel N. Shorah: estimating the genetic diversity of a mixed sample from next-generation sequencing data. BMC Bioinf. 2011; 12(1):119.
    • (2011) BMC Bioinf. , vol.12 , Issue.1 , pp. 119
    • Zagordi, O.1    Bhattacharya, A.2    Eriksson, N.3    Beerenwinkel, N.4
  • 6
    • 84855173088 scopus 로고    scopus 로고
    • Qure: software for viral quasispecies reconstruction from next-generation sequencing data
    • Prosperi MC, Salemi M. Qure: software for viral quasispecies reconstruction from next-generation sequencing data. Bioinformatics. 2012; 28(1):132-3.
    • (2012) Bioinformatics. , vol.28 , Issue.1 , pp. 132-133
    • Prosperi, M.C.1    Salemi, M.2
  • 9
    • 52649157765 scopus 로고    scopus 로고
    • Substantial biases in ultra-short read data sets from high-throughput dna sequencing
    • Dohm JC, Lottaz C, Borodina T, Himmelbauer H. Substantial biases in ultra-short read data sets from high-throughput dna sequencing. Nucleic Acids Res. 2008; 36(16):105.
    • (2008) Nucleic Acids Res. , vol.36 , Issue.16 , pp. 105
    • Dohm, J.C.1    Lottaz, C.2    Borodina, T.3    Himmelbauer, H.4
  • 10
    • 84871227763 scopus 로고    scopus 로고
    • Lofreq: a sequence-quality aware, ultra-sensitive variant caller for uncovering cell-population heterogeneity from high-throughput sequencing datasets
    • Wilm A, Aw PPK, Bertrand D, Yeo GHT, Ong SH, Wong CH, et al. Lofreq: a sequence-quality aware, ultra-sensitive variant caller for uncovering cell-population heterogeneity from high-throughput sequencing datasets. Nucleic Acids Res. 2012:918.
    • (2012) Nucleic Acids Res. , pp. 918
    • Wilm, A.1    Aw, P.P.K.2    Bertrand, D.3    Yeo, G.H.T.4    Ong, S.H.5    Wong, C.H.6
  • 11
    • 84861108474 scopus 로고    scopus 로고
    • Highly sensitive and specific detection of rare variants in mixed viral populations from massively parallel sequence data
    • Macalalad AR, Zody MC, Charlebois P, Lennon NJ, Newman RM, Malboeuf CM, et al. Highly sensitive and specific detection of rare variants in mixed viral populations from massively parallel sequence data. PLoS Comput Biol. 2012; 8(3):1002417.
    • (2012) PLoS Comput Biol. , vol.8 , Issue.3 , pp. 1002417
    • Macalalad, A.R.1    Zody, M.C.2    Charlebois, P.3    Lennon, N.J.4    Newman, R.M.5    Malboeuf, C.M.6
  • 14
    • 84938969775 scopus 로고    scopus 로고
    • Roche 454
    • Roche 454. http://www.genomeweb.com/sequencing/roche-shutting-down-454-sequencing-business.
  • 15
    • 0031978181 scopus 로고    scopus 로고
    • Base-calling of automated sequencer traces using phred. ii. error probabilities
    • Ewing B, Green P. Base-calling of automated sequencer traces using phred. ii. error probabilities. Genome Res. 1998; 8(3):186-94.
    • (1998) Genome Res. , vol.8 , Issue.3 , pp. 186-194
    • Ewing, B.1    Green, P.2
  • 16
  • 18
    • 77956837921 scopus 로고    scopus 로고
    • Model-based quality assessment and base-calling for second-generation sequencing data
    • Bravo HC, Irizarry RA. Model-based quality assessment and base-calling for second-generation sequencing data. Biometrics. 2010; 66(3):665-74.
    • (2010) Biometrics. , vol.66 , Issue.3 , pp. 665-674
    • Bravo, H.C.1    Irizarry, R.A.2
  • 20
    • 84938973408 scopus 로고    scopus 로고
    • Manual Illumina
    • Manual Illumina. http://supportres.illumina.com/documents/myillumina/ec3129a6-b41f-4d98-963f-668391997f1a/olb_194_userguide_15009920d.pdf.
  • 21
    • 67649884743 scopus 로고    scopus 로고
    • Fast and accurate short read alignment with burrows-wheeler transform
    • Li H, Durbin R. Fast and accurate short read alignment with burrows-wheeler transform. Bioinformatics. 2009; 25(14):1754-60.
    • (2009) Bioinformatics. , vol.25 , Issue.14 , pp. 1754-1760
    • Li, H.1    Durbin, R.2
  • 22
    • 84900810127 scopus 로고    scopus 로고
    • Benchmarking of viral haplotype reconstruction programmes: an overview of the capacities and limitations of currently available programmes
    • Schirmer M, Sloan WT, Quince C. Benchmarking of viral haplotype reconstruction programmes: an overview of the capacities and limitations of currently available programmes. Brief Bioinf. 2014; 15(3):431-42.
    • (2014) Brief Bioinf. , vol.15 , Issue.3 , pp. 431-442
    • Schirmer, M.1    Sloan, W.T.2    Quince, C.3
  • 24
    • 0035998835 scopus 로고    scopus 로고
    • Model-based clustering, discriminant analysis, and density estimation
    • Fraley C, Raftery AE. Model-based clustering, discriminant analysis, and density estimation. J Am Stat Assoc. 2002; 97(458):611-31.
    • (2002) J Am Stat Assoc. , vol.97 , Issue.458 , pp. 611-631
    • Fraley, C.1    Raftery, A.E.2
  • 25
    • 78650928878 scopus 로고    scopus 로고
    • New direct-acting antivirals' combination for the treatment of chronic hepatitis c
    • Asselah T, Marcellin P. New direct-acting antivirals' combination for the treatment of chronic hepatitis c. Liver International. 2011; 31(s1):68-77.
    • (2011) Liver International. , vol.31 , pp. 68-77
    • Asselah, T.1    Marcellin, P.2
  • 26
    • 78649901946 scopus 로고    scopus 로고
    • Error correction of next-generation sequencing data and reliable estimation of hiv quasispecies
    • Zagordi O, Klein R, Däumer M, Beerenwinkel N. Error correction of next-generation sequencing data and reliable estimation of hiv quasispecies. Nucleic Acids Res. 2010; 38(21):7400-9.
    • (2010) Nucleic Acids Res. , vol.38 , Issue.21 , pp. 7400-7409
    • Zagordi, O.1    Klein, R.2    Däumer, M.3    Beerenwinkel, N.4
  • 27
    • 84861214061 scopus 로고    scopus 로고
    • Whole genome deep sequencing of hiv-1 reveals the impact of early minor variants upon immune recognition during acute infection
    • Henn MR, Boutwell CL, Charlebois P, Lennon NJ, Power KA, Macalalad AR, et al. Whole genome deep sequencing of hiv-1 reveals the impact of early minor variants upon immune recognition during acute infection. PLoS Pathogens. 2012; 8(3):1002529.
    • (2012) PLoS Pathogens. , vol.8 , Issue.3 , pp. 1002529
    • Henn, M.R.1    Boutwell, C.L.2    Charlebois, P.3    Lennon, N.J.4    Power, K.A.5    Macalalad, A.R.6
  • 28
    • 84938958117 scopus 로고    scopus 로고
    • Local variants
    • Local variants. https://github.com/ozagordi/localvariants.
  • 29
    • 79956314887 scopus 로고    scopus 로고
    • Genotype and snp calling from next-generation sequencing data
    • Nielsen R, Paul JS, Albrechtsen A, Song YS. Genotype and snp calling from next-generation sequencing data. Nat Rev Genet. 2011; 12(6):443-51.
    • (2011) Nat Rev Genet. , vol.12 , Issue.6 , pp. 443-451
    • Nielsen, R.1    Paul, J.S.2    Albrechtsen, A.3    Song, Y.S.4
  • 30
    • 84900323186 scopus 로고    scopus 로고
    • Prevalence and evolution of low frequency hiv drug resistance mutations detected by ultra deep sequencing in patients experiencing first line antiretroviral therapy failure
    • Vandenhende M-A, Bellecave P, Recordon-Pinson P, Reigadas S, Bidet Y, Bruyand M, et al. Prevalence and evolution of low frequency hiv drug resistance mutations detected by ultra deep sequencing in patients experiencing first line antiretroviral therapy failure. PloS One. 2014; 9(1):86771.
    • (2014) PloS One. , vol.9 , Issue.1 , pp. 86771
    • Vandenhende, M.-A.1    Bellecave, P.2    Recordon-Pinson, P.3    Reigadas, S.4    Bidet, Y.5    Bruyand, M.6
  • 31
    • 79958830099 scopus 로고    scopus 로고
    • Hepatitis c virus resistance to protease inhibitors
    • Halfon P, Locarnini S. Hepatitis c virus resistance to protease inhibitors. J Hepatol. 2011; 55(1):192-206.
    • (2011) J Hepatol. , vol.55 , Issue.1 , pp. 192-206
    • Halfon, P.1    Locarnini, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.