-
1
-
-
52649157765
-
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
-
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
-
3
-
-
44949250815
-
Viral population estimation using pyrosequencing
-
Eriksson N, Pachter L, Mitsuya Y, Rhee S-Y, Wang C, Gharizadeh B, et al. Viral population estimation using pyrosequencing. PLoS Comput Biol. 2008; 4(5):1000074.
-
(2008)
PLoS Comput Biol.
, vol.4
, Issue.5
, pp. 1000074
-
-
Eriksson, N.1
Pachter, L.2
Mitsuya, Y.3
Rhee, S.-Y.4
Wang, C.5
Gharizadeh, B.6
-
4
-
-
77950840976
-
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
-
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
-
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
-
7
-
-
84855286473
-
Ultrasensitive detection of rare mutations using next-generation targeted resequencing
-
Flaherty P, Natsoulis G, Muralidharan O, Winters M, Buenrostro J, Bell J, et al. Ultrasensitive detection of rare mutations using next-generation targeted resequencing. Nucleic Acids Res. 2012; 40(1):e2.
-
(2012)
Nucleic Acids Res.
, vol.40
, Issue.1
, pp. e2
-
-
Flaherty, P.1
Natsoulis, G.2
Muralidharan, O.3
Winters, M.4
Buenrostro, J.5
Bell, J.6
-
8
-
-
43149107930
-
Quality scores and snp detection in sequencing-by-synthesis systems
-
Brockman W, Alvarez P, Young S, Garber M, Giannoukos G, Lee WL, et al. Quality scores and snp detection in sequencing-by-synthesis systems. Genome Res. 2008; 18(5):763-70.
-
(2008)
Genome Res.
, vol.18
, Issue.5
, pp. 763-770
-
-
Brockman, W.1
Alvarez, P.2
Young, S.3
Garber, M.4
Giannoukos, G.5
Lee, W.L.6
-
9
-
-
52649157765
-
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
-
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
-
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
-
12
-
-
84884893391
-
V-phaser 2: variant inference for viral populations
-
Yang X, Charlebois P, Macalalad A, Henn MR, Zody MC. V-phaser 2: variant inference for viral populations. BMC Genomics. 2013; 14(1):674.
-
(2013)
BMC Genomics.
, vol.14
, Issue.1
, pp. 674
-
-
Yang, X.1
Charlebois, P.2
Macalalad, A.3
Henn, M.R.4
Zody, M.C.5
-
13
-
-
79251565226
-
Removing noise from pyrosequenced amplicons
-
Quince C, Lanzen A, Davenport RJ, Turnbaugh PJ. Removing noise from pyrosequenced amplicons. BMC Bioinf. 2011; 12(1):38.
-
(2011)
BMC Bioinf.
, vol.12
, Issue.1
, pp. 38
-
-
Quince, C.1
Lanzen, A.2
Davenport, R.J.3
Turnbaugh, P.J.4
-
14
-
-
84938969775
-
-
Roche 454
-
Roche 454. http://www.genomeweb.com/sequencing/roche-shutting-down-454-sequencing-business.
-
-
-
-
15
-
-
0031978181
-
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
-
-
84868687174
-
Improved base-calling and quality scores for 454 sequencing based on a hurdle poisson model
-
De Beuf K, Schrijver JD, Thas O, Criekinge WV, Irizarry RA, Clement L. Improved base-calling and quality scores for 454 sequencing based on a hurdle poisson model. BMC Bioinf. 2012; 13(1):303.
-
(2012)
BMC Bioinf.
, vol.13
, Issue.1
, pp. 303
-
-
De Beuf, K.1
Schrijver, J.D.2
Thas, O.3
Criekinge, W.V.4
Irizarry, R.A.5
Clement, L.6
-
17
-
-
55549089660
-
Accurate whole human genome sequencing using reversible terminator chemistry
-
Bentley DR, Balasubramanian S, Swerdlow HP, Smith GP, Milton J, Brown CG, et al. Accurate whole human genome sequencing using reversible terminator chemistry. Nature. 2008; 456(7218):53-9.
-
(2008)
Nature.
, vol.456
, Issue.7218
, pp. 53-59
-
-
Bentley, D.R.1
Balasubramanian, S.2
Swerdlow, H.P.3
Smith, G.P.4
Milton, J.5
Brown, C.G.6
-
18
-
-
77956837921
-
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
-
19
-
-
84859749487
-
Analysis of context-dependent errors for illumina sequencing
-
Abnizova I, Leonard S, Skelly T, Brown A, Jackson D, Gourtovaia M, et al. Analysis of context-dependent errors for illumina sequencing. J Bioinf Comput Biol. 2012; 10(02):1241005.
-
(2012)
J Bioinf Comput Biol.
, vol.10
, Issue.2
, pp. 1241005
-
-
Abnizova, I.1
Leonard, S.2
Skelly, T.3
Brown, A.4
Jackson, D.5
Gourtovaia, M.6
-
20
-
-
84938973408
-
-
Manual Illumina
-
Manual Illumina. http://supportres.illumina.com/documents/myillumina/ec3129a6-b41f-4d98-963f-668391997f1a/olb_194_userguide_15009920d.pdf.
-
-
-
-
21
-
-
67649884743
-
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
-
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
-
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
-
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
-
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
-
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
-
-
Local variants
-
Local variants. https://github.com/ozagordi/localvariants.
-
-
-
-
29
-
-
79956314887
-
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
-
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
-
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
|