-
1
-
-
13144306071
-
Genome-wide association studies for common diseases and complex traits
-
Hirschhorn, J. and Daly, M. (2005) Genome-wide association studies for common diseases and complex traits. Nat. Rev. Genet., 6, 95-108.
-
(2005)
Nat. Rev. Genet.
, vol.6
, pp. 95-108
-
-
Hirschhorn, J.1
Daly, M.2
-
2
-
-
20244380171
-
Complement factor H polymorphism in age-related macular degeneration
-
Klein, R., Zeiss, C., Chew, E., Tsai, J., Sackler, R., Haynes, C., Henning, A., SanGiovanni, J., Mane, S., Mayne, S.T. et al. (2005) Complement factor H polymorphism in age-related macular degeneration. Science, 308, 385-389.
-
(2005)
Science
, vol.308
, pp. 385-389
-
-
Klein, R.1
Zeiss, C.2
Chew, E.3
Tsai, J.4
Sackler, R.5
Haynes, C.6
Henning, A.7
SanGiovanni, J.8
Mane, S.9
Mayne, S.T.10
-
3
-
-
84969213492
-
Genome-wide association study of 14, 000 cases of seven common diseases and 3,000 shared controls
-
Burton, P., Clayton, D., Cardon, L., Craddock, N., Deloukas, P., Duncanson, A., Kwiatkowski, D., McCarthy, M., Ouwehand, W., Samani, N. et al. (2007) Genome-wide association study of 14, 000 cases of seven common diseases and 3, 000 shared controls. Nature, 447, 661-678.
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
Burton, P.1
Clayton, D.2
Cardon, L.3
Craddock, N.4
Deloukas, P.5
Duncanson, A.6
Kwiatkowski, D.7
McCarthy, M.8
Ouwehand, W.9
Samani, N.10
-
4
-
-
33847176604
-
A genome-wide association study identifies novel risk loci for type 2 diabetes
-
Sladek, R., Rocheleau, G., Rung, J., Dina, C., Shen, L., Serre, D., Boutin, P., Vincent, D., Belisle, A., Hadjadj, S. et al. (2007) A genome-wide association study identifies novel risk loci for type 2 diabetes. Nature, 445, 881-885.
-
(2007)
Nature
, vol.445
, pp. 881-885
-
-
Sladek, R.1
Rocheleau, G.2
Rung, J.3
Dina, C.4
Shen, L.5
Serre, D.6
Boutin, P.7
Vincent, D.8
Belisle, A.9
Hadjadj, S.10
-
5
-
-
3843056691
-
Multiple rare alleles contribute to low plasma levels of HDL cholesterol
-
Cohen, J., Kiss, R., Pertsemlidis, A., Marcel, Y., McPherson, R. and Hobbs, H. (2004) Multiple rare alleles contribute to low plasma levels of HDL cholesterol. Science, 305, 869-872.
-
(2004)
Science
, vol.305
, pp. 869-872
-
-
Cohen, J.1
Kiss, R.2
Pertsemlidis, A.3
Marcel, Y.4
McPherson, R.5
Hobbs, H.6
-
6
-
-
33847759937
-
Schizophrenia: a common disease caused by multiple rare alleles
-
McClellan, J., Susser, E. and King, M. (2007) Schizophrenia: a common disease caused by multiple rare alleles. Br. J. Psychiatry, 190, 194-199.
-
(2007)
Br. J. Psychiatry
, vol.190
, pp. 194-199
-
-
McClellan, J.1
Susser, E.2
King, M.3
-
7
-
-
44349132708
-
Common and rare variants in multifactorial susceptibility to common diseases
-
Bodmer, W. and Bonilla, C. (2008) Common and rare variants in multifactorial susceptibility to common diseases. Nat. Genet., 40, 695-701.
-
(2008)
Nat. Genet.
, vol.40
, pp. 695-701
-
-
Bodmer, W.1
Bonilla, C.2
-
8
-
-
67149117126
-
Discovery of rare variants via sequencing: implications for the design of complex trait association studies
-
Li, B. and Leal, S. (2009) Discovery of rare variants via sequencing: implications for the design of complex trait association studies. PLoS Genet., 5, e1000481.
-
(2009)
PLoS Genet.
, vol.5
-
-
Li, B.1
Leal, S.2
-
9
-
-
39649117755
-
The impact of next-generation sequencing technology on genetics
-
2008
-
Mardis, E. (2008) The impact of next-generation sequencing technology on genetics. Trends Genet., 24, 133-141, 2008.
-
(2008)
Trends Genet.
, vol.24
, pp. 133-141
-
-
Mardis, E.1
-
10
-
-
24044455869
-
Genome sequencing in microfabricated high-density picolitre reactors
-
Margulies, M., Egholm, M., Altman, W., Attiya, S., Bader, J., Bemben, L., Berka, J., Braverman, M., Chen, Y., Chen, Z. et al. (2005) Genome sequencing in microfabricated high-density picolitre reactors. Nature, 437, 376-380.
-
(2005)
Nature
, vol.437
, pp. 376-380
-
-
Margulies, M.1
Egholm, M.2
Altman, W.3
Attiya, S.4
Bader, J.5
Bemben, L.6
Berka, J.7
Braverman, M.8
Chen, Y.9
Chen, Z.10
-
11
-
-
2442674039
-
Decoding randomly ordered DNA arrays
-
Gunderson, K., Kruglyak, S., Graige, M., Garcia, F., Kermani, B., Zhao, C., Che, D., Dickinson, T., Wickham, E., Bierle, J. et al. (2004) Decoding randomly ordered DNA arrays. Genome Res., 14, 870-877.
-
(2004)
Genome Res.
, vol.14
, pp. 870-877
-
-
Gunderson, K.1
Kruglyak, S.2
Graige, M.3
Garcia, F.4
Kermani, B.5
Zhao, C.6
Che, D.7
Dickinson, T.8
Wickham, E.9
Bierle, J.10
-
12
-
-
41749104588
-
Single-molecule DNA sequencing of a viral genome
-
Harris, T., Buzby, P., Babcock, H., Beer, E., Bowers, J., Braslavsky, I., Causey, M., Colonell, J., DiMeo, J., Efcavitch, J. et al. (2008) Single-molecule DNA sequencing of a viral genome. Science, 320, 106-109.
-
(2008)
Science
, vol.320
, pp. 106-109
-
-
Harris, T.1
Buzby, P.2
Babcock, H.3
Beer, E.4
Bowers, J.5
Braslavsky, I.6
Causey, M.7
Colonell, J.8
DiMeo, J.9
Efcavitch, J.10
-
13
-
-
67650323916
-
Targeted resequencing and analysis of the Diamond-Blackfan anemia disease locus RPS 19
-
Martinez, B., Eriksson, O., Badhai, J., Frjmark, A.-S., Bongcam-Rudloff, E., Dahl, N. and Schuster, J. (2009) Targeted resequencing and analysis of the Diamond-Blackfan anemia disease locus RPS 19 PLoS ONE, 4, e6172.
-
(2009)
PLoS ONE
, vol.4
-
-
Martinez, B.1
Eriksson, O.2
Badhai, J.3
Frjmark, A.-S.4
Bongcam-Rudloff, E.5
Dahl, N.6
Schuster, J.7
-
14
-
-
77956323966
-
Deep sequencing of target linkage assay-identified regions in familial breast cancer: methods, analysis pipeline and troubleshooting
-
Rosa-Rosa, J., Gracia-Aznrez, F., Hodges, E., Pita, G., Rooks, M., Xuan, Z., Bhattacharjee, A., Brizuela, L., Silva, J., Hannon, G. et al. (2010) Deep sequencing of target linkage assay-identified regions in familial breast cancer: methods, analysis pipeline and troubleshooting. PLoS ONE, 5, e9976.
-
(2010)
PLoS ONE
, vol.5
-
-
Rosa-Rosa, J.1
Gracia-Aznrez, F.2
Hodges, E.3
Pita, G.4
Rooks, M.5
Xuan, Z.6
Bhattacharjee, A.7
Brizuela, L.8
Silva, J.9
Hannon, G.10
-
15
-
-
78049361216
-
Target-enrichment strategies for next-generation sequencing
-
Mamanova, L., Coffey, A., Scott, C., Kozarewa, I., Turner, E., Kumar, A., Howard, E., Shendure, J. and Turner, D. (2009) Target-enrichment strategies for next-generation sequencing. Nat. Meth., 110, 471-478.
-
(2009)
Nat. Meth.
, vol.110
, pp. 471-478
-
-
Mamanova, L.1
Coffey, A.2
Scott, C.3
Kozarewa, I.4
Turner, E.5
Kumar, A.6
Howard, E.7
Shendure, J.8
Turner, D.9
-
16
-
-
35748951614
-
Direct selection of human genomic loci by microarray hybridization
-
Albert, T., Molla, M., Muzny, D., Nazareth, L., Wheeler, D., Song, X., Richmond, T., Middle, C., Rodesch, M., Packard, C. et al. (2007) Direct selection of human genomic loci by microarray hybridization. Nat. Meth., 4, 903-905.
-
(2007)
Nat. Meth.
, vol.4
, pp. 903-905
-
-
Albert, T.1
Molla, M.2
Muzny, D.3
Nazareth, L.4
Wheeler, D.5
Song, X.6
Richmond, T.7
Middle, C.8
Rodesch, M.9
Packard, C.10
-
17
-
-
59849113821
-
Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing
-
Gnirke, A., Melnikov, A., Maguire, J., Rogov, P., LeProust, E., Brockman, W., Fennell, T., Giannoukos, G., Fisher, S., Russ, C. et al. (2009) Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing. Nat. Biotechnol., 27, 182-189.
-
(2009)
Nat. Biotechnol.
, vol.27
, pp. 182-189
-
-
Gnirke, A.1
Melnikov, A.2
Maguire, J.3
Rogov, P.4
LeProust, E.5
Brockman, W.6
Fennell, T.7
Giannoukos, G.8
Fisher, S.9
Russ, C.10
-
18
-
-
70249111091
-
Targeted capture and massively parallel sequencing of 12 human exomes
-
Ng, S., Turner, E., Robertson, P., Flygare, S., Bigham, A., Lee, C., Shaffer, T., Wong, M., Bhattacharjee, A., Eichler, E. et al. (2009) Targeted capture and massively parallel sequencing of 12 human exomes. Nature, 461, 272-276.
-
(2009)
Nature
, vol.461
, pp. 272-276
-
-
Ng, S.1
Turner, E.2
Robertson, P.3
Flygare, S.4
Bigham, A.5
Lee, C.6
Shaffer, T.7
Wong, M.8
Bhattacharjee, A.9
Eichler, E.10
-
19
-
-
0036590151
-
Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools
-
Norton, N., Williams, N., Williams, H., Spurlock, G., Kirov, G., Morris, D., Hoogendoorn, B., Owen, M. and O'Donovan, M. (2002) Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools. Hum. Genet., 110, 471-478.
-
(2002)
Hum. Genet.
, vol.110
, pp. 471-478
-
-
Norton, N.1
Williams, N.2
Williams, H.3
Spurlock, G.4
Kirov, G.5
Morris, D.6
Hoogendoorn, B.7
Owen, M.8
O'Donovan, M.9
-
20
-
-
36549088042
-
Association mapping using pooled DNA
-
Yang, H. and Fann, C. (2007) Association mapping using pooled DNA. Meth. Mol. Biol., 376, 161-175.
-
(2007)
Meth. Mol. Biol.
, vol.376
, pp. 161-175
-
-
Yang, H.1
Fann, C.2
-
21
-
-
0031889566
-
Allele frequency distributions in pooled DNA samples: applications to mapping complex disease genes
-
Shaw, S., Carrasquillo, M., Kashuk, C., Puffenberger, E. and Chakravarti, A. (1998) Allele frequency distributions in pooled DNA samples: applications to mapping complex disease genes. Genome Res., 8, 111-123.
-
(1998)
Genome Res.
, vol.8
, pp. 111-123
-
-
Shaw, S.1
Carrasquillo, M.2
Kashuk, C.3
Puffenberger, E.4
Chakravarti, A.5
-
23
-
-
67650034261
-
Overlapping pools for high-throughput targeted resequencing
-
Prabhu, S. and Pe'er, I. (2009) Overlapping pools for high-throughput targeted resequencing. Genome Res., 19, 1254-1261.
-
(2009)
Genome Res.
, vol.19
, pp. 1254-1261
-
-
Prabhu, S.1
Pe'er, I.2
-
24
-
-
0005476664
-
New results in the theory of superimposed codes
-
Bansko, Bulgaria
-
D'yachkov, A.G., Macula, A., Torney, D., Vilenkin, P. and Yekhanin, S. (2000) New results in the theory of superimposed codes. Proceedings of International Workshop on Algebraic and Combinatorial Coding Theory (ACCT). Bansko, Bulgaria, pp. 126-136.
-
(2000)
Proceedings of International Workshop on Algebraic and Combinatorial Coding Theory (ACCT)
, pp. 126-136
-
-
D'yachkov, A.G.1
Macula, A.2
Torney, D.3
Vilenkin, P.4
Yekhanin, S.5
-
26
-
-
65749101850
-
Weighted superimposed codes and constrained integer compressed sensing
-
Dai, W. and Milenkovic, O. (2009) Weighted superimposed codes and constrained integer compressed sensing. IEEE Trans. Inf. Theory, 55, 2215-2229.
-
(2009)
IEEE Trans. Inf. Theory
, vol.55
, pp. 2215-2229
-
-
Dai, W.1
Milenkovic, O.2
-
27
-
-
67650047735
-
DNA Sudoku-harnessing high-throughput sequencing for multiplexed specimen analysis
-
Erlich, Y., Chang, K., Gordon, A., Ronen, R., Navon, O., Rooks, M. and Hannon, G. (2009) DNA Sudoku-harnessing high-throughput sequencing for multiplexed specimen analysis. Genome Res., 19, 1243-1253.
-
(2009)
Genome Res.
, vol.19
, pp. 1243-1253
-
-
Erlich, Y.1
Chang, K.2
Gordon, A.3
Ronen, R.4
Navon, O.5
Rooks, M.6
Hannon, G.7
-
28
-
-
70349696280
-
Group testing and sparse signal recovery
-
Monterey, CA. IEEE Signal Processing Society, Piscataway, NJ, USA
-
Gilbert, A., Iwen, M. and Strauss, M. (2008) Group testing and sparse signal recovery. In 42nd Asilomar Conference on Signals, Systems, and Computers, Monterey, CA. IEEE Signal Processing Society, Piscataway, NJ, USA.
-
(2008)
42nd Asilomar Conference on Signals, Systems, and Computers
-
-
Gilbert, A.1
Iwen, M.2
Strauss, M.3
-
29
-
-
77952737626
-
Compressed Genotyping
-
Erlich, Y., Gordon, A., Brand, M., Hannon, G. and Mitra, P. (2009) Compressed Genotyping. Arxiv preprint Quantitative Biology/0909.3691.
-
(2009)
Arxiv preprint Quantitative Biology/0909.
, pp. 3691
-
-
Erlich, Y.1
Gordon, A.2
Brand, M.3
Hannon, G.4
Mitra, P.5
-
31
-
-
33645712892
-
Compressed sensing
-
Donoho, D. (2006) Compressed sensing. IEEE Trans. Inf. Theory, 52, 1289-1306.
-
(2006)
IEEE Trans. Inf. Theory
, vol.52
, pp. 1289-1306
-
-
Donoho, D.1
-
32
-
-
36849088522
-
Sparse MRI: the application of compressed sensing for rapid MR imaging
-
Lustig, M., Donoho, D. and Pauly, J. (2007) Sparse MRI: the application of compressed sensing for rapid MR imaging. Magn. Reson. Med., 58, 1182-1195.
-
(2007)
Magn. Reson. Med.
, vol.58
, pp. 1182-1195
-
-
Lustig, M.1
Donoho, D.2
Pauly, J.3
-
33
-
-
85032752277
-
Single-pixel imaging via compressive sampling
-
Duarte, M., Davenport, M., Takhar, D., Laska, J., Sun, T., Kelly, K. and Baraniuk, R. (2008) Single-pixel imaging via compressive sampling. IEEE Signal Process. Mag., 25, 83-91.
-
(2008)
IEEE Signal Process. Mag.
, vol.25
, pp. 83-91
-
-
Duarte, M.1
Davenport, M.2
Takhar, D.3
Laska, J.4
Sun, T.5
Kelly, K.6
Baraniuk, R.7
-
34
-
-
34548525109
-
Compressed wavefield extrapolation
-
Lin, T. and Herrmann, F. (2007) Compressed wavefield extrapolation. Geophysics, 72, SM77-SM93.
-
(2007)
Geophysics
, vol.72
-
-
Lin, T.1
Herrmann, F.2
-
35
-
-
57949117273
-
Compressed sensing in astronomy
-
Bobin, J., Starck, J. and Ottensamer, R. (2008) Compressed sensing in astronomy. J. Sel. Top. Signal Process., 2, 718-726.
-
(2008)
J. Sel. Top. Signal Process.
, vol.2
, pp. 718-726
-
-
Bobin, J.1
Starck, J.2
Ottensamer, R.3
-
36
-
-
59849117352
-
Compressive sensing DNA microarrays
-
Dai, W., Sheikh, M., Milenkovic, O. and Baraniuk, R. (2009) Compressive sensing DNA microarrays. EURASIP J. Bioinform. Syst. Biol., 2009, 162824.
-
(2009)
EURASIP J. Bioinform. Syst. Biol.
, vol.2009
, pp. 162824
-
-
Dai, W.1
Sheikh, M.2
Milenkovic, O.3
Baraniuk, R.4
-
37
-
-
78650826512
-
NESTA: a fast and accurate first-order method for sparse recovery
-
arXiv:0904.3367
-
Becker, S., Bobin, J. and Candes, E. (2009) NESTA: a fast and accurate first-order method for sparse recovery. Arxiv preprint arXiv:0904.3367.
-
(2009)
Arxiv preprint
-
-
Becker, S.1
Bobin, J.2
Candes, E.3
-
38
-
-
71749099456
-
Deep sequencing to reveal new variants in pooled DNA samples
-
Out, A., van Minderhout, I., Goeman, J., Ariyurek, Y., Ossowski, S., Schneeberger, K., Weigal, D., van Galen, M., Taschner, P., Tops, C. et al. (2009) Deep sequencing to reveal new variants in pooled DNA samples. Hum. Mutat., 30, 1703-1712.
-
(2009)
Hum. Mutat.
, vol.30
, pp. 1703-1712
-
-
Out, A.1
van Minderhout, I.2
Goeman, J.3
Ariyurek, Y.4
Ossowski, S.5
Schneeberger, K.6
Weigal, D.7
van Galen, M.8
Taschner, P.9
Tops, C.10
-
39
-
-
29144439194
-
Decoding by linear programming
-
Candes, E. and Tao, T. (2005) Decoding by linear programming. IEEE Trans. Inf. Theory, 51, 4203-4215.
-
(2005)
IEEE Trans. Inf. Theory
, vol.51
, pp. 4203-4215
-
-
Candes, E.1
Tao, T.2
-
40
-
-
78049373242
-
Stable signal recovery from incomplete and inaccurate measurements
-
math/0503066
-
Candes, E., Romberg, J. and Tao, T. (2005) Stable signal recovery from incomplete and inaccurate measurements. Arxiv preprint math/0503066.
-
(2005)
Arxiv preprint
-
-
Candes, E.1
Romberg, J.2
Tao, T.3
-
41
-
-
33646365077
-
For most large underdetermined systems of linear equations the minimal l1-norm solution is also the sparsest solution
-
Donoho, D. (2006) For most large underdetermined systems of linear equations the minimal l1-norm solution is also the sparsest solution. Commun. Pure Appl. Math., 59, 797-829.
-
(2006)
Commun. Pure Appl. Math.
, vol.59
, pp. 797-829
-
-
Donoho, D.1
-
42
-
-
33947416035
-
Near-optimal signal recovery from random projections: universal encoding strategies?
-
Candes, E. and Tao, T. (2006) Near-optimal signal recovery from random projections: universal encoding strategies? IEEE Trans. Inf. Theory, 52, 5406-5425.
-
(2006)
IEEE Trans. Inf. Theory
, vol.52
, pp. 5406-5425
-
-
Candes, E.1
Tao, T.2
-
43
-
-
33748540464
-
Error correction via linear programming
-
Wiley-IEEE Computer Society Press, Hoboken USA
-
Candes, E., Rudelson, M., Tao, T. and Vershynin, R. (2005) Error correction via linear programming. In Annual Symposium on Foundations of Computer Science, Vol. 46. Wiley-IEEE Computer Society Press, Hoboken, USA, pp. 295-308.
-
(2005)
Annual Symposium on Foundations of Computer Science
, vol.46
, pp. 295-308
-
-
Candes, E.1
Rudelson, M.2
Tao, T.3
Vershynin, R.4
-
44
-
-
39449126969
-
Gradient projection for sparse reconstruction: application to compressed sensing and other inverse problems
-
Figueiredo, M., Nowak, R. and Wright, S. (2007) Gradient projection for sparse reconstruction: application to compressed sensing and other inverse problems. IEEE J. Sel. Top. Signal Process., 1, 586-597.
-
(2007)
IEEE J. Sel. Top. Signal Process.
, vol.1
, pp. 586-597
-
-
Figueiredo, M.1
Nowak, R.2
Wright, S.3
-
45
-
-
22144488449
-
Sparse nonnegative solution of underdetermined linear equations by linear programming
-
Donoho, D. and Tanner, J. (2005) Sparse nonnegative solution of underdetermined linear equations by linear programming. Proc. Natl Acad. Sci. USA, 102, 9446-9451.
-
(2005)
Proc. Natl Acad. Sci. USA
, vol.102
, pp. 9446-9451
-
-
Donoho, D.1
Tanner, J.2
-
46
-
-
60749100685
-
SNP frequency estimation using massively parallel sequencing of pooled DNA
-
Ingman, M. and Gyllensten, U. (2009) SNP frequency estimation using massively parallel sequencing of pooled DNA. Eur. J. Hum. Genet., 17, 383-386.
-
(2009)
Eur. J. Hum. Genet.
, vol.17
, pp. 383-386
-
-
Ingman, M.1
Gyllensten, U.2
-
47
-
-
55549097836
-
Mapping short DNA sequencing reads and calling variants using mapping quality scores
-
Li, H., Ruan, J. and Durbin, R. (2008) Mapping short DNA sequencing reads and calling variants using mapping quality scores. Genome Res., 18, 1851-1858.
-
(2008)
Genome Res.
, vol.18
, pp. 1851-1858
-
-
Li, H.1
Ruan, J.2
Durbin, R.3
-
48
-
-
0032894224
-
Quantitative RT-PCR: pitfalls and potential
-
Freeman, W., Walker, S. and Vrana, K. (1999) Quantitative RT-PCR: pitfalls and potential. Biotechniques, 26, 112-125.
-
(1999)
Biotechniques
, vol.26
, pp. 112-125
-
-
Freeman, W.1
Walker, S.2
Vrana, K.3
-
49
-
-
70349646530
-
BayesCall: a model-based base-calling algorithm for high-throughput short-read sequencing
-
Kao, W., Stevens, K. and Song, Y. (2009) BayesCall: a model-based base-calling algorithm for high-throughput short-read sequencing. Genome Res., 19, 1884-1895.
-
(2009)
Genome Res.
, vol.19
, pp. 1884-1895
-
-
Kao, W.1
Stevens, K.2
Song, Y.3
-
50
-
-
33947636650
-
Most pooling variation in array-based DNA pooling is attributable to array error rather than pool construction error
-
Macgregor, S. (2007) Most pooling variation in array-based DNA pooling is attributable to array error rather than pool construction error. Eur. J. Hum. Genet., 15, 501-504.
-
(2007)
Eur. J. Hum. Genet.
, vol.15
, pp. 501-504
-
-
Macgregor, S.1
-
51
-
-
39449109476
-
An interior-point method for large-scale l1-regularized least squares
-
Kim, S., Koh, K., Lustig, M., Boyd, S. and Gorinevsky, D. (2007) An interior-point method for large-scale l1-regularized least squares. IEEE J. Sel. Top. Signal Process., 1, 606-617.
-
(2007)
IEEE J. Sel. Top. Signal Process.
, vol.1
, pp. 606-617
-
-
Kim, S.1
Koh, K.2
Lustig, M.3
Boyd, S.4
Gorinevsky, D.5
-
52
-
-
40149103278
-
Error-correcting barcoded primers for pyrosequencing hundreds of samples in multiplex
-
Hamady, M., Walker, J., Harris, J., Gold, N. and Knight, R. (2008) Error-correcting barcoded primers for pyrosequencing hundreds of samples in multiplex. Nat. Meth., 5, 235-237.
-
(2008)
Nat. Meth.
, vol.5
, pp. 235-237
-
-
Hamady, M.1
Walker, J.2
Harris, J.3
Gold, N.4
Knight, R.5
-
54
-
-
44849087307
-
Bayesian compressive sensing
-
Ji, S., Xue, Y. and Carin, L. (2008) Bayesian compressive sensing. IEEE Trans. Signal Process., 56, 2346-2356.
-
(2008)
IEEE Trans. Signal Process.
, vol.56
, pp. 2346-2356
-
-
Ji, S.1
Xue, Y.2
Carin, L.3
-
55
-
-
72949124697
-
Bayesian compressive sensing via belief propagation
-
Baron, D., Sarvatham, S. and Baraniuk, R. (2010) Bayesian compressive sensing via belief propagation. IEEE Trans. Signal Process., 58, 269-280.
-
(2010)
IEEE Trans. Signal Process.
, vol.58
, pp. 269-280
-
-
Baron, D.1
Sarvatham, S.2
Baraniuk, R.3
-
56
-
-
43149107930
-
Quality scores and SNP detection in sequencing-by-synthesis systems
-
Brockman, W., Alvarez, P., Young, S., Garber, M., Giannoukos, G., Lee, W., Russ, C., Lander, E., Nusbaum, C. and Jaffe, D. (2008) Quality scores and SNP detection in sequencing-by-synthesis systems. Genome Res., 18, 763.
-
(2008)
Genome Res.
, vol.18
, pp. 763
-
-
Brockman, W.1
Alvarez, P.2
Young, S.3
Garber, M.4
Giannoukos, G.5
Lee, W.6
Russ, C.7
Lander, E.8
Nusbaum, C.9
Jaffe, D.10
-
57
-
-
77956295988
-
The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data
-
McKenna, A.H., Hanna, M., Banks, E., Sivachenko, A., Cibulskis, K., Kernytsky, A., Garimella, K., Altshuler, D., Gabriel, S., Daly, M. et al. (2010) The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res.
-
(2010)
Genome Res.
-
-
McKenna, A.H.1
Hanna, M.2
Banks, E.3
Sivachenko, A.4
Cibulskis, K.5
Kernytsky, A.6
Garimella, K.7
Altshuler, D.8
Gabriel, S.9
Daly, M.10
|