-
1
-
-
0017681196
-
DNA sequencing with chain-terminating inhibitors
-
Sanger, F., Nicklen, S., and Coulson, A. (1977) DNA sequencing with chain-terminating inhibitors. Proceedings of the National Academy of Sciences of the United States of America, 74, 5463.
-
(1977)
Proceedings of the National Academy of Sciences of the United States of America
, vol.74
, pp. 5463
-
-
Sanger, F.1
Nicklen, S.2
Coulson, A.3
-
2
-
-
42249087308
-
The complete genome of an individual by massively parallel DNA sequencing
-
Wheeler, D., et al. (2008) The complete genome of an individual by massively parallel DNA sequencing. Nature, 452, 872-876.
-
(2008)
Nature
, vol.452
, pp. 872-876
-
-
Wheeler, D.1
-
3
-
-
55549089660
-
Accurate whole human genome sequencing using reversible terminator chemistry
-
Bentley, D., et al. (2008) Accurate whole human genome sequencing using reversible terminator chemistry. Nature, 456, 53-59.
-
(2008)
Nature
, vol.456
, pp. 53-59
-
-
Bentley, D.1
-
4
-
-
55549097849
-
The diploid genome sequence of an Asian individual
-
Wang, J., et al. (2008) The diploid genome sequence of an Asian individual. Nature, 456, 60-65.
-
(2008)
Nature
, vol.456
, pp. 60-65
-
-
Wang, J.1
-
5
-
-
69249232047
-
A highly annotated whole-genome sequence of a Korean individual
-
Kim, J., et al. (2009) A highly annotated whole-genome sequence of a Korean individual. Nature, 460, 1011-1015.
-
(2009)
Nature
, vol.460
, pp. 1011-1015
-
-
Kim, J.1
-
6
-
-
34547633677
-
Genome-wide profiles of STAT1 DNA association using chromatin immunoprecipitation and massively parallel sequencing
-
Robertson, G., et al. (2007) Genome-wide profiles of STAT1 DNA association using chromatin immunoprecipitation and massively parallel sequencing. Nature Methods, 4, 651-657.
-
(2007)
Nature Methods
, vol.4
, pp. 651-657
-
-
Robertson, G.1
-
7
-
-
57749195712
-
RNA-Seq: A revolutionary tool for transcriptomics
-
Wang, Z., Gerstein, M., and Snyder,M. (2009) RNA-Seq: a revolutionary tool for transcriptomics. Nature Reviews Genetics, 10, 57-63.
-
(2009)
Nature Reviews Genetics
, vol.10
, pp. 57-63
-
-
Wang, Z.1
Gerstein, M.2
Snyder, M.3
-
8
-
-
70450217879
-
Human DNA methylomes at base resolution show widespread epigenomic differences
-
Lister, R., et al. (2009) Human DNA methylomes at base resolution show widespread epigenomic differences. Nature, 462, 315-322.
-
(2009)
Nature
, vol.462
, pp. 315-322
-
-
Lister, R.1
-
9
-
-
70249111091
-
Targeted capture and assively parallel sequencing of 12 human exomes
-
Ng, S., et al. (2009) Targeted capture and assively parallel sequencing of 12 human exomes. Nature, 461, 272-276.
-
(2009)
Nature
, vol.461
, pp. 272-276
-
-
Ng, S.1
-
10
-
-
0032540905
-
A sequencing method based on real-time pyrophosphate
-
Washington
-
Ronaghi, M., Uhlen, M., and Nyren, P. (1998) A sequencing method based on real-time pyrophosphate. Science(Washington), 281, 363-365.
-
(1998)
Science
, vol.281
, pp. 363-365
-
-
Ronaghi, M.1
Uhlen, M.2
Nyren, P.3
-
11
-
-
0034130561
-
Gene expression analysis by massively parallel signature sequencing MPSS on microbead arrays
-
Brenner, S., et al. (2000) Gene expression analysis by massively parallel signature sequencing (MPSS) on microbead arrays. Nature biotechnology, 18, 630-634.
-
(2000)
Nature Biotechnology
, vol.18
, pp. 630-634
-
-
Brenner, S.1
-
12
-
-
34948842866
-
Accuracy and quality of massively parallel DNA pyrosequencing
-
Huse, S., Huber, J., Morrison, H., Sogin, M., and Welch, D. (2007) Accuracy and quality of massively parallel DNA pyrosequencing. Genome Biology, 8, R143.
-
(2007)
Genome Biology
, vol.8
-
-
Huse, S.1
Huber, J.2
Morrison, H.3
Sogin, M.4
Welch, D.5
-
13
-
-
77952886150
-
Assembly algorithms for next-generation sequencing data
-
Miller, J., Koren, S., and Sutton, G. (2010) Assembly algorithms for next-generation sequencing data. Genomics, 95, 315-327.
-
(2010)
Genomics
, vol.95
, pp. 315-327
-
-
Miller, J.1
Koren, S.2
Sutton, G.3
-
14
-
-
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 Research, 18, 1851.
-
(2008)
Genome Research
, vol.18
, pp. 1851
-
-
Li, H.1
Ruan, J.2
Durbin, R.3
-
15
-
-
62349130698
-
Ultra-fast and memoryefficient alignment of short DNA sequences to the human genome
-
Langmead, B., Trapnell, C., Pop, M., and Salzberg, S. (2009) Ultra-fast and memoryefficient alignment of short DNA sequences to the human genome. Genome Biol, 10, R25.
-
(2009)
Genome Biol.
, vol.10
-
-
Langmead, B.1
Trapnell, C.2
Pop, M.3
Salzberg, S.4
-
16
-
-
77949587649
-
Fast and accurate long-read alignment with burrows-wheeler transform
-
Li, H. and Durbin, R. (2010) Fast and accurate long-read alignment with Burrows-Wheeler transform. Bioinformatics, 26, 589.
-
(2010)
Bioinformatics
, vol.26
, pp. 589
-
-
Li, H.1
Durbin, R.2
-
17
-
-
70349556543
-
Personalized copy number and segmental duplication maps using next-generation sequencing
-
Alkan, C., et al. (2009) Personalized copy number and segmental duplication maps using next-generation sequencing. Nature Genetics, 41, 1061-1067.
-
(2009)
Nature Genetics
, vol.41
, pp. 1061-1067
-
-
Alkan, C.1
-
18
-
-
70450177746
-
Bfast: An alignment tool for large scale genome resequencing
-
Homer, N., Merriman, B., and Nelson, S. (2009) BFAST: an alignment tool for large scale genome resequencing. PLoSOne, 4, e7767.
-
(2009)
PLoS One
, vol.4
-
-
Homer, N.1
Merriman, B.2
Nelson, S.3
-
19
-
-
40049104732
-
Soap: Short oligonucleotide alignment program
-
Li, R., Li, Y., Kristiansen, K., and Wang, J. (2008) SOAP: short oligonucleotide alignment program. Bioinformatics, 24, 713.
-
(2008)
Bioinformatics
, vol.24
, pp. 713
-
-
Li, R.1
Li, Y.2
Kristiansen, K.3
Wang, J.4
-
20
-
-
34547295064
-
Jigsaw puzzles edge matching and polyomino packing: Connections and complexity
-
Demaine, E. and Demaine, M. (2007) Jigsaw puzzles, edge matching, and polyomino packing: Connections and complexity. Graphs and Combinatorics, 23, 195-208.
-
(2007)
Graphs and Combinatorics
, vol.23
, pp. 195-208
-
-
Demaine, E.1
Demaine, M.2
-
21
-
-
0018426987
-
A strategy of DNA sequencing employing computer programs
-
Staden, R. (1979) A strategy of DNA sequencing employing computer programs. Nucleic Acids Research, 6, 2601.
-
(1979)
Nucleic Acids Research
, vol.6
, pp. 2601
-
-
Staden, R.1
-
22
-
-
0023988195
-
Genomic mapping by finger-printing random clones: A mathematical analysis
-
Lander, E. andWaterman, M. (1988) Genomic mapping by finger-printing random clones: a mathematical analysis. Genomics, 2, 231-239.
-
(1988)
Genomics
, vol.2
, pp. 231-239
-
-
Lander, E.1
Waterman, M.2
-
23
-
-
0029312158
-
Toward simplifying and accurately formulating fragment assembly
-
Myers, E. (1995) Toward simplifying and accurately formulating fragment assembly. Journal of Computational Biology, 2, 275-290.
-
(1995)
Journal of Computational Biology
, vol.2
, pp. 275-290
-
-
Myers, E.1
-
25
-
-
0001899550
-
TIGR Assembler: A new tool for assembling large shotgun sequencing projects
-
Sutton, G., White, O., Adams, M., and Kerlavage, A. (1995) TIGR Assembler: A new tool for assembling large shotgun sequencing projects. Genome Science and Technology, 1, 9-19.
-
(1995)
Genome Science and Technology
, vol.1
, pp. 9-19
-
-
Sutton, G.1
White, O.2
Adams, M.3
Kerlavage, A.4
-
26
-
-
0032849859
-
CAP3: A DNA sequence assembly program
-
Huang, X. and Madan, A. (1999) CAP3: A DNA sequence assembly program. Genome research, 9, 868.
-
(1999)
Genome research
, vol.9
, pp. 868
-
-
Huang, X.1
Madan, A.2
-
27
-
-
0034708758
-
A whole-genome assembly of drosophila
-
Myers, E., et al. (2000) A whole-genome assembly of Drosophila. Science, 287, 2196.
-
(2000)
Science
, vol.287
, pp. 2196
-
-
Myers, E.1
-
29
-
-
0035859921
-
An eulerian path approach to DNA fragment assembly
-
Pevzner, P., Tang, H., and Waterman, M. (2001) An Eulerian path approach to DNA fragment assembly. Proceedings of the National Academy of Sciences of the United States ofAmerica, 98, 9748.
-
(2001)
Proceedings of the National Academy of Sciences of the United States of America
, vol.98
, pp. 9748
-
-
Pevzner, P.1
Tang, H.2
Waterman, M.3
-
30
-
-
0346505466
-
Hierarchical scaffolding with bambus
-
Pop, M., Kosack, D., and Salzberg, S. (2004) Hierarchical scaffolding with Bambus. Genome Research, 14, 149.
-
(2004)
Genome Research
, vol.14
, pp. 149
-
-
Pop, M.1
Kosack, D.2
Salzberg, S.3
-
31
-
-
77957758142
-
Reptile: Representative tiling for short read error correction
-
Yang, X., Dorman, K., and Aluru, S. (2010) Reptile: Representative Tiling for Short Read Error Correction. Bioinformatics, 26, 2526
-
(2010)
Bioinformatics
, vol.26
, pp. 2526
-
-
Yang, X.1
Dorman, K.2
Aluru, S.3
-
32
-
-
78649358717
-
Quake: Quality-aware detection and correction of sequencing errors
-
Kelley, D., Schatz, M., and Salzberg, S. (2010) Quake: quality-aware detection and correction of sequencing errors. Genome Biology, 11, R116.
-
(2010)
Genome Biology
, vol.11
-
-
Kelley, D.1
Schatz, M.2
Salzberg, S.3
-
33
-
-
45549109750
-
Genome assembly forensics: Finding the elusive mis-assembly
-
Phillippy, A., Schatz, M., and Pop, M. (2008) Genome assembly forensics: finding the elusive mis-assembly. Genome Biology, 9, R55.
-
(2008)
Genome Biology
, vol.9
-
-
Phillippy, A.1
Schatz, M.2
Pop, M.3
-
34
-
-
40749116115
-
A machinelearningapproach to combined evidence validation of genome assemblies
-
Choi, J., Kim, S., Tang, H., Andrews, J., Gilbert, D., and Colbourne, J. (2008) A machinelearningapproach to combined evidence validation of genome assemblies. Bioinformatics, 24, 744.
-
(2008)
Bioinformatics
, vol.24
, pp. 744
-
-
Choi, J.1
Kim, S.2
Tang, H.3
Andrews, J.4
Gilbert, D.5
Colbourne, J.6
-
35
-
-
0031955116
-
Consed: A graphical tool for sequence finishing
-
Gordon, D., Abajian, C., and Green, P. (1998) Consed: a graphical tool for sequence finishing. Genome Research, 8, 195.
-
(1998)
Genome Research
, vol.8
, pp. 195
-
-
Gordon, D.1
Abajian, C.2
Green, P.3
-
36
-
-
77649253051
-
Visualizing genomes: Techniques and challenges
-
Nielsen, C., Cantor, M., Dubchak, I., Gordon, D., and Wang, T. (2010) Visualizing genomes: techniques and challenges. Nature Methods, 7 S5-S15.
-
(2010)
Nature Methods
, vol.7
-
-
Nielsen, C.1
Cantor, M.2
Dubchak, I.3
Gordon, D.4
Wang, T.5
-
37
-
-
34250210806
-
Hawkeye: An interactive visual analytics tool for genome assemblies
-
Schatz, M., Phillippy, A., Shneiderman, B., and Salzberg, S. (2007) Hawkeye: an interactive visual analytics tool for genome assemblies. Genome Biology, 8, R34.
-
(2007)
Genome Biology
, vol.8
-
-
Schatz, M.1
Phillippy, A.2
Shneiderman, B.3
Salzberg, S.4
-
38
-
-
41249098849
-
A high quality draft consensus sequence of the genome of a heterozygous grapevine variety
-
Velasco, R., et al. (2007) A high quality draft consensus sequence of the genome of a heterozygous grapevine variety. PLoS One, 2, 1326.
-
(2007)
PLoS One
, vol.2
, pp. 1326
-
-
Velasco, R.1
-
39
-
-
33746605947
-
A sanger pyrosequencing hybrid approach for the generation of high-quality draft assemblies of marine microbial genomes
-
Goldberg, S., et al. (2006) A Sanger/pyrosequencing hybrid approach for the generation of high-quality draft assemblies of marine microbial genomes. Proceedings of the National Academy of Sciences, 103, 11240.
-
(2006)
Proceedings of the National Academy of Sciences
, vol.103
, pp. 11240
-
-
Goldberg, S.1
-
40
-
-
70649085835
-
The genome of the cucumber cucumis sativus L
-
Huang, S., et al. (2009) The genome of the cucumber, Cucumis sativus L. Nature Genetics, 41, 1275-1281.
-
(2009)
Nature Genetics
, vol.41
, pp. 1275-1281
-
-
Huang, S.1
-
41
-
-
59949090259
-
De novo assembly using low-coverage short read sequence data from the rice pathogen pseudomonas syringae pv oryzae
-
Reinhardt, J., Baltrus, D., Nishimura, M., Jeck, W., Jones, C., and Dangl, J. (2009) De novo assembly using low-coverage short read sequence data from the rice pathogen Pseudomonas syringae pv. oryzae. Genome Research, 19, 294.
-
(2009)
Genome Research
, vol.19
, pp. 294
-
-
Reinhardt, J.1
Baltrus, D.2
Nishimura, M.3
Jeck, W.4
Jones, C.5
Dangl, J.6
-
42
-
-
46249087524
-
A robust framework for detecting structural variations in a genome
-
Lee, S., Cheran, E., and Brudno, M. (2008) A robust framework for detecting structural variations in a genome. Bioinformatics, 24, i59.
-
(2008)
Bioinformatics
, vol.24
-
-
Lee, S.1
Cheran, E.2
Brudno, M.3
-
43
-
-
67650064593
-
Combinatorial algorithms for structural variation detection in highthroughput sequenced genomes
-
Hormozdiari, F., Alkan, C., Eichler, E., and Sahinalp, S. (2009) Combinatorial algorithms for structural variation detection in highthroughput sequenced genomes. Genome Research, 19, 1270.
-
(2009)
Genome Research
, vol.19
, pp. 1270
-
-
Hormozdiari, F.1
Alkan, C.2
Eichler, E.3
Sahinalp, S.4
-
44
-
-
67649580757
-
MoDIL: Detecting small indels from clone-end sequencing with mixtures of distributions
-
Lee, S.,Hormozdiari, F., Alkan,C., and Brudno, M. (2009) MoDIL: detecting small indels from clone-end sequencing with mixtures of distributions. Nature Methods, 6, 473-474.
-
(2009)
Nature Methods
, vol.6
, pp. 473-474
-
-
Lee, S.1
Hormozdiari, F.2
Alkan, C.3
Brudno, M.4
-
45
-
-
69549116107
-
Break dancer: An algorithm for high-resolution mapping of genomic structural variation
-
Chen, K., et al. (2009) BreakDancer: an algorithm for high-resolution mapping of genomic structural variation. Nature Methods, 6, 677-681.
-
(2009)
Nature Methods
, vol.6
, pp. 677-681
-
-
Chen, K.1
-
46
-
-
70350694443
-
Pindel: A pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads
-
Ye, K., Schulz, M., Long, Q., Apweiler, R., and Ning, Z. (2009) Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads. Bioinformatics, 25, 2865.
-
(2009)
Bioinformatics
, vol.25
, pp. 2865
-
-
Ye, K.1
Schulz, M.2
Long, Q.3
Apweiler, R.4
Ning, Z.5
-
47
-
-
16644381328
-
Comparative genome assembly
-
Pop, M., Phillippy, A., Delcher, A., and Salzberg, S. (2004) Comparative genome assembly. Briefings in Bioinformatics, 5, 237.
-
(2004)
Briefings in Bioinformatics
, vol.5
, pp. 237
-
-
Pop, M.1
Phillippy, A.2
Delcher, A.3
Salzberg, S.4
-
48
-
-
52949083195
-
Gene-boosted assembly of a novel bacterial genome from very short reads
-
Salzberg, S., Sommer, D., Puiu, D., and Lee, V. (2008) Gene-boosted assembly of a novel bacterial genome from very short reads. PLoS Comput Biol, 4, e1000186.
-
(2008)
PLoS Comput. Biol.
, vol.4
-
-
Salzberg, S.1
Sommer, D.2
Puiu, D.3
Lee, V.4
-
49
-
-
49549099085
-
HapCUT: An efficient and accurate algorithm for the haplotype assembly problem
-
Bansal, V. and Bafna, V. (2008) HapCUT: an efficient and accurate algorithm for the haplotype assembly problem. Bioinformatics, 24, i153.
-
(2008)
Bioinformatics
, vol.24
-
-
Bansal, V.1
Bafna, V.2
-
50
-
-
35648976118
-
The diploid genome sequence of an individual human
-
Levy, S., et al. (2007) The diploid genome sequence of an individual human. PLoS Biol, 5, e254.
-
(2007)
PLoS Biol.
, vol.5
-
-
Levy, S.1
-
52
-
-
79953815355
-
Optimal spliced alignments of short sequence reads
-
De Bona, F., Ossowski, S., Schneeberger, K., and Ratsch, G. (2008) Optimal spliced alignments of short sequence reads. BMC Bioinformatics, 9, O7.
-
(2008)
BMC Bioinformatics
, vol.9
-
-
De Bona, F.1
Ossowski, S.2
Schneeberger, K.3
Ratsch, G.4
-
53
-
-
65449136284
-
Tophat: Discovering splice junctions with RNA-Seq
-
Trapnell, C., Pachter, L., and Salzberg, S. (2009) TopHat: discovering splice junctions with RNA-Seq. Bioinformatics, 25, 1105.
-
(2009)
Bioinformatics
, vol.25
, pp. 1105
-
-
Trapnell, C.1
Pachter, L.2
Salzberg, S.3
-
54
-
-
78649345104
-
Map splice: Accurate mapping of RNA-seq reads for splice junction discovery
-
Wang, K., et al. (2010) MapSplice: Accurate mapping of RNA-seq reads for splice junction discovery. Nucleic Acids Research, 38, e178.
-
(2010)
Nucleic Acids Research
, vol.38
-
-
Wang, K.1
-
55
-
-
77952123055
-
Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoformswitching during cell differentiation
-
Trapnell, C., Williams, B., Pertea, G., Mortazavi, A., Kwan, G., Van Baren, M., Salzberg, S., Wold, B., and Pachter, L. (2010) Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoformswitching during cell differentiation. NatureBiotechnology, 28, 511-515.
-
(2010)
Nature Biotechnology
, vol.28
, pp. 511-515
-
-
Trapnell, C.1
Williams, B.2
Pertea, G.3
Mortazavi, A.4
Kwan, G.5
Van Baren, M.6
Salzberg, S.7
Wold, B.8
Pachter, L.9
-
56
-
-
33847307402
-
Assembling millions of short DNA sequences using SSAKE
-
Warren, R., Sutton, G., Jones, S., and Holt, R. (2007) Assembling millions of short DNA sequences using SSAKE. Bioinformatics, 23,500.
-
(2007)
Bioinformatics
, vol.23
, pp. 500
-
-
Warren, R.1
Sutton, G.2
Jones, S.3
Holt, R.4
-
57
-
-
36448948250
-
Extending assembly of short DNA sequences to handle error
-
Jeck, W., Reinhardt, J., Baltrus, D., Hickenbotham,M., Magrini, V., Mardis, E., Dangl, J., and Jones, C. (2007) Extending assembly of short DNA sequences to handle error. Bioinformatics, 23, 2942.
-
(2007)
Bioinformatics
, vol.23
, pp. 2942
-
-
Jeck, W.1
Reinhardt, J.2
Baltrus, D.3
Hickenbotham, M.4
Magrini, V.5
Mardis, E.6
Dangl, J.7
Jones, C.8
-
58
-
-
36448948250
-
Extending assembly of short DNA sequences to handle error
-
Jeck, W., Reinhardt, J., Baltrus, D., Hickenbotham, M., Magrini, V., Mardis, E., Dangl, J., and Jones, C. (2007) Extending assembly ofshort DNA sequences to handle error. Bioinformatics, 23, 2942.
-
(2007)
Bioinformatics
, vol.23
, pp. 2942
-
-
Jeck, W.1
Reinhardt, J.2
Baltrus, D.3
Hickenbotham, M.4
Magrini, V.5
Mardis, E.6
Dangl, J.7
Jones, C.8
-
59
-
-
0036144823
-
Arachne: A wholegenome shotgun assembler
-
Batzoglou, S., Jaffe, D., Stanley, K., Butler, J.,Gnerre, S., Mauceli, E., Berger, B., Mesirov, J.,and Lander, E. (2002) ARACHNE: a wholegenome shotgun assembler. Genome Research, 12, 177.
-
(2002)
Genome Research
, vol.12
, pp. 177
-
-
Batzoglou, S.1
Jaffe, D.2
Stanley, K.3
Butler, J.4
Gnerre, S.5
Mauceli, E.6
Berger, B.7
Mesirov, J.8
Lander, E.9
-
60
-
-
0037267048
-
Whole-genome sequenceassembly for mammalian genomes: Arachne 2
-
Jaffe, D., Butler, J., Gnerre, S., Mauceli, E., Lindblad-Toh, K., Mesirov, J., Zody, M., andLander, E. (2003) Whole-genome sequenceassembly for mammalian genomes: Arachne 2.Genome Research, 13, 91.
-
(2003)
Genome Research
, vol.13
, pp. 91
-
-
Jaffe, D.1
Butler, J.2
Gnerre, S.3
Mauceli, E.4
Lindblad-Toh, K.5
Mesirov, J.6
Zody, M.7
Lander, E.8
-
61
-
-
3042615882
-
Using the miraEST assembler for reliableand automated mRNA transcript assemblyand SNP detection in sequenced ESTs
-
Chevreux, B., Pfisterer, T., Drescher, B., Driesel,A., Muller, W., Wetter, T., and Suhai, S.(2004) Using the miraEST assembler for reliableand automated mRNA transcript assemblyand SNP detection in sequenced ESTs. GenomeResearch, 14, 1147.
-
(2004)
Genome Research
, vol.14
, pp. 1147
-
-
Chevreux, B.1
Pfisterer, T.2
Drescher, B.3
Driesel, A.4
Muller, W.5
Wetter, T.6
Suhai, S.7
-
63
-
-
39049156065
-
Short read fragment assembly of bacterial genomes
-
Chaisson, M. and Pevzner, P. (2008) Short read fragment assembly of bacterial genomes.Genome Research, 18, 324.
-
(2008)
Genome Research
, vol.18
, pp. 324
-
-
Chaisson, M.1
Pevzner, P.2
-
64
-
-
43149115851
-
Velvet: Algorithms for de novo short read assembly usingde bruijn graphs
-
Zerbino, D. and Birney, E. (2008) Velvet: algorithms for de novo short read assembly usingde Bruijn graphs. Genome Research, 18, 821.
-
(2008)
Genome Research
, vol.18
, pp. 821
-
-
Zerbino, D.1
Birney, E.2
-
65
-
-
43149086380
-
Allpaths: De novo assembly of whole-genome shotgun microreads
-
Butler, J., MacCallum, I., Kleber, M., Shlyakhter, I., Belmonte, M., Lander, E., Nusbaum,C., and Jaffe, D. (2008) ALLPATHS: de novo assembly of whole-genome shotgun microreads.Genome Research, 18, 810.
-
(2008)
Genome Research
, vol.18
, pp. 810
-
-
Butler, J.1
MacCallum, I.2
Kleber, M.3
Shlyakhter, I.4
Belmonte, M.5
Lander, E.6
Nusbaum, C.7
Jaffe, D.8
-
66
-
-
66449136667
-
ABySS: A parallel assembler for short read sequence data
-
Simpson, J., Wong, K., Jackman, S., Schein, J., Jones, S., and Birol, I. (2009) ABySS: A parallel assembler for short read sequence data. Genome Research, 19, 1117.
-
(2009)
Genome Research
, vol.19
, pp. 1117
-
-
Simpson, J.1
Wong, K.2
Jackman, S.3
Schein, J.4
Jones, S.5
Birol, I.6
-
67
-
-
75649124547
-
De novo assembly ofhuman genomes with massively parallel short read sequencing
-
Li, R., et al. (2010) De novo assembly ofhuman genomes with massively parallel short read sequencing. Genome Research, 20, 265
-
(2010)
Genome Research
, vol.20
, pp. 265
-
-
Li, R.1
|