-
1
-
-
84975742565
-
Amap of human genome variation from population-scale sequencing
-
1000 Genomes Proj. Consort
-
1000 Genomes Proj. Consort. 2010. Amap of human genome variation from population-scale sequencing. Nature 467:1061-73
-
(2010)
Nature
, vol.467
, pp. 1061-1073
-
-
-
3
-
-
0029028720
-
Genotypic analysis ofmultiple loci in somatic cells by whole genome amplification
-
Barrett MT, Reid BJ, Joslyn G. 1995. Genotypic analysis ofmultiple loci in somatic cells by whole genome amplification. Nucleic Acids Res. 23:3488-92
-
(1995)
Nucleic Acids Res
, vol.23
, pp. 3488-3492
-
-
Barrett, M.T.1
Reid, B.J.2
Joslyn, G.3
-
4
-
-
55549089660
-
Accurate whole human genome sequencing using reversible terminator chemistry
-
Bentley DR, Balasubramanian S, Swerdlow HP, Smith GP, Milton J, 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.R.1
Balasubramanian, S.2
Swerdlow, H.P.3
Smith, G.P.4
Milton, J.5
-
5
-
-
0024335104
-
Highly efficient DNA synthesis by the phage ω29 DNA polymerase: Symmetrical mode of DNA replication
-
Blanco L, Bernad A, Lázaro JM, Martin G, Garmendia C, Salas M. 1989. Highly efficient DNA synthesis by the phage ω29 DNA polymerase: symmetrical mode of DNA replication. J. Biol. Chem. 264:8935-40
-
(1989)
J. Biol. Chem
, vol.264
, pp. 8935-8940
-
-
Blanco, L.1
Bernad, A.2
Lázaro, J.M.3
Martin, G.4
Garmendia, C.5
Salas, M.6
-
6
-
-
84926429952
-
Single cell transcriptome amplification with MALBAC
-
Chapman AR, He Z, Lu S, Yong J, Tan L, et al. 2015. Single cell transcriptome amplification with MALBAC. PLOS ONE 10:e0120889
-
(2015)
PLOS ONE
, vol.10
, pp. e0120889
-
-
Chapman, A.R.1
He, Z.2
Lu, S.3
Yong, J.4
Tan, L.5
-
7
-
-
0029966845
-
Whole genome amplification using a degenerate oligonucleotide primer allows hundreds of genotypes to be performed on less than one nanogram of genomic DNA
-
Cheung VG, Nelson SF. 1996. Whole genome amplification using a degenerate oligonucleotide primer allows hundreds of genotypes to be performed on less than one nanogram of genomic DNA. PNAS 93:14676-79
-
(1996)
PNAS
, vol.93
, pp. 14676-14679
-
-
Cheung, V.G.1
Nelson, S.F.2
-
8
-
-
33845746387
-
An evolutionary view of human recombination
-
Coop G, Przeworski M. 2007. An evolutionary view of human recombination. Nat. Rev. Genet. 8:23-34
-
(2007)
Nat. Rev. Genet
, vol.8
, pp. 23-34
-
-
Coop, G.1
Przeworski, M.2
-
9
-
-
84905502594
-
Rapid phenotypic and genomic change in response to therapeutic pressure in prostate cancer inferred by high content analysis of single circulating tumor cells
-
Dago AE, Stepansky A, Carlsson A, Luttgen M, Kendall J, et al. 2014. Rapid phenotypic and genomic change in response to therapeutic pressure in prostate cancer inferred by high content analysis of single circulating tumor cells. PLOS ONE 9:e101777
-
(2014)
PLOS ONE
, vol.9
, pp. e101777
-
-
Dago, A.E.1
Stepansky, A.2
Carlsson, A.3
Luttgen, M.4
Kendall, J.5
-
10
-
-
84879797164
-
First successful double-factor PGD for Lynch syndrome: Monogenic analysis and comprehensive aneuploidy screening
-
Daina G, Ramos L, Obradors A, Rius M, Martinez-Pasarell O, et al. 2013. First successful double-factor PGD for Lynch syndrome: monogenic analysis and comprehensive aneuploidy screening. Clin. Genet. 84:70-73
-
(2013)
Clin. Genet
, vol.84
, pp. 70-73
-
-
Daina, G.1
Ramos, L.2
Obradors, A.3
Rius, M.4
Martinez-Pasarell, O.5
-
11
-
-
84920645442
-
A quantitative comparison of single-cell whole genome amplification methods
-
de Bourcy CF, De Vlaminck I, Kanbar JN,Wang J,Gawad C, Quake SR. 2014. A quantitative comparison of single-cell whole genome amplification methods. PLOS ONE 9:e105585
-
(2014)
PLOS ONE
, vol.9
, pp. e105585
-
-
De Bourcy, C.F.1
De Vlaminck, I.2
Kanbar, J.N.3
Wang, J.4
Gawad, C.5
Quake, S.R.6
-
12
-
-
0034830935
-
Rapid amplification of plasmid and phageDNA using phi29 DNA polymerase and multiply-primed rolling circle amplification
-
Dean FB,Nelson JR, Giesler TL, Lasken RS. 2001. Rapid amplification of plasmid and phageDNA using phi29 DNA polymerase and multiply-primed rolling circle amplification. Genome Res. 11:1095-99
-
(2001)
Genome Res
, vol.11
, pp. 1095-1099
-
-
Dean, F.B.1
Nelson, J.R.2
Giesler, T.L.3
Lasken, R.S.4
-
15
-
-
84905447834
-
EGFR variant heterogeneity in glioblastoma resolved through single-nucleus sequencing
-
Francis JM, Zhang CZ, Maire CL, Jung J, Manzo VE, et al. 2014. EGFR variant heterogeneity in glioblastoma resolved through single-nucleus sequencing. Cancer Discov. 4:956-971
-
(2014)
Cancer Discov
, vol.4
, pp. 956-971
-
-
Francis, J.M.1
Zhang, C.Z.2
Maire, C.L.3
Jung, J.4
Manzo, V.E.5
-
16
-
-
35348983887
-
A second generation human haplotype map of over 3
-
Frazer KA, Ballinger DG, Cox DR, Hinds DA, Stuve LL, et al. 2007. A second generation human haplotype map of over 3.1 million SNPs. Nature 449:851-61
-
(2007)
1 Million SNPs. Nature
, vol.449
, pp. 851-861
-
-
Frazer, K.A.1
Ballinger, D.G.2
Cox, D.R.3
Hinds, D.A.4
Stuve, L.L.5
-
17
-
-
0026794640
-
The bacteriophageω29 DNA polymerase, a proofreading enzyme
-
Garmendia C, Bernad A, Esteban JA, Blanco L, Salas M. 1992. The bacteriophageω29 DNA polymerase, a proofreading enzyme. J. Biol. Chem. 267:2594-99
-
(1992)
J. Biol. Chem
, vol.267
, pp. 2594-2599
-
-
Garmendia, C.1
Bernad, A.2
Esteban, J.A.3
Blanco, L.4
Salas, M.5
-
18
-
-
84919372228
-
Dissecting the clonal origins of childhood acute lymphoblastic leukemia by single-cell genomics
-
Gawad C, Koh W, Quake SR. 2014. Dissecting the clonal origins of childhood acute lymphoblastic leukemia by single-cell genomics. PNAS 111:17947-52
-
(2014)
PNAS
, vol.111
, pp. 17947-17952
-
-
Gawad, C.1
Koh, W.2
Quake, S.R.3
-
19
-
-
84890526238
-
Single-cellmethylome landscapes of mouse embryonic stem cells and early embryos analyzed using reduced representation bisulfite sequencing
-
GuoH, Zhu P,WuX, Li X, Wen L,Tang F. 2013. Single-cellmethylome landscapes of mouse embryonic stem cells and early embryos analyzed using reduced representation bisulfite sequencing. Genome Res. 23:2126-35
-
(2013)
Genome Res
, vol.23
, pp. 2126-2135
-
-
Guo, H.1
Zhu, P.2
Wu, X.3
Li, X.4
Wen, L.5
Tang, F.6
-
20
-
-
41749104588
-
Single-molecule DNA sequencing of a viral genome
-
Harris TD, Buzby PR, Babcock H, Beer E, Bowers J, et al. 2008. Single-molecule DNA sequencing of a viral genome. Science 320:106-9
-
(2008)
Science
, vol.320
, pp. 106-109
-
-
Harris, T.D.1
Buzby, P.R.2
Babcock, H.3
Beer, E.4
Bowers, J.5
-
23
-
-
80051679387
-
The landscape of recombination in African Americans
-
Hinch AG, Tandon A, Patterson N, Song Y, Rohland N, et al. 2011. The landscape of recombination in African Americans. Nature 476:170-75
-
(2011)
Nature
, vol.476
, pp. 170-175
-
-
Hinch, A.G.1
Tandon, A.2
Patterson, N.3
Song, Y.4
Rohland, N.5
-
24
-
-
84893594630
-
Genome analyses of single human oocytes
-
Hou Y, Fan W, Yan L, Li R, Lian Y, et al. 2013. Genome analyses of single human oocytes. Cell 155:1492-506
-
(2013)
Cell
, vol.155
, pp. 1492-1506
-
-
Hou, Y.1
Fan, W.2
Yan, L.3
Li, R.4
Lian, Y.5
-
25
-
-
84863229772
-
Single-cell exome sequencing and monoclonal evolution of a JAK2-negative myeloproliferative neoplasm
-
Hou Y, Song L, Zhu P, Zhang B, Tao Y, et al. 2012. Single-cell exome sequencing and monoclonal evolution of a JAK2-negative myeloproliferative neoplasm. Cell 148:873-85
-
(2012)
Cell
, vol.148
, pp. 873-885
-
-
Hou, Y.1
Song, L.2
Zhu, P.3
Zhang, B.4
Tao, Y.5
-
26
-
-
84921971016
-
Validation of multiple annealing and loopingbased amplification cycle sequencing for 24-chromosome aneuploidy screening of cleavage-stage embryos
-
Huang J, Yan L, Fan W, Zhao N, Zhang Y, et al. 2014. Validation of multiple annealing and loopingbased amplification cycle sequencing for 24-chromosome aneuploidy screening of cleavage-stage embryos. Fertil. Steril. 102:1685-91
-
(2014)
Fertil. Steril
, vol.102
, pp. 1685-1691
-
-
Huang, J.1
Yan, L.2
Fan, W.3
Zhao, N.4
Zhang, Y.5
-
27
-
-
4444291843
-
Detection of large-scale variation in the human genome
-
Iafrate AJ, Feuk L, RiveraMN, ListewnikML, Donahoe PK, et al. 2004. Detection of large-scale variation in the human genome. Nat. Genet. 36:949-51
-
(2004)
Nat. Genet
, vol.36
, pp. 949-951
-
-
Iafrate, A.J.1
Feuk, L.2
Rivera, M.N.3
Listewnik, M.L.4
Donahoe, P.K.5
-
28
-
-
33646757738
-
Compound and double mutations in patients with hypertrophic cardiomyopathy: Implications for genetic testing and counselling
-
Ingles J, Doolan A, Chiu C, Seidman J, Seidman C, Semsarian C. 2005. Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling. J. Med. Genet. 42:e59
-
(2005)
J. Med. Genet
, vol.42
, pp. e59
-
-
Ingles, J.1
Doolan, A.2
Chiu, C.3
Seidman, J.4
Seidman, C.5
Semsarian, C.6
-
29
-
-
79959524146
-
A haplotype map of the human genome
-
Int. HapMap Consort
-
Int. HapMap Consort. 2005. A haplotype map of the human genome. Nature 437:1299-320
-
(2005)
Nature
, vol.437
, pp. 1299-1320
-
-
-
30
-
-
0036649022
-
Reciprocal crossover asymmetry and meiotic drive in a human recombination hot spot
-
Jeffreys AJ, Neumann R. 2002. Reciprocal crossover asymmetry and meiotic drive in a human recombination hot spot. Nat. Genet. 31:267-71
-
(2002)
Nat. Genet
, vol.31
, pp. 267-271
-
-
Jeffreys, A.J.1
Neumann, R.2
-
32
-
-
84877156149
-
Sequencing of isolated sperm cells for direct haplotyping of a human genome
-
Kirkness EF, Grindberg RV, Yee-Greenbaum J, Marshall CR, Scherer SW, et al. 2013. Sequencing of isolated sperm cells for direct haplotyping of a human genome. Genome Res. 23:826-32
-
(2013)
Genome Res
, vol.23
, pp. 826-832
-
-
Kirkness, E.F.1
Grindberg, R.V.2
Yee-Greenbaum, J.3
Marshall, C.R.4
Scherer, S.W.5
-
33
-
-
78651333227
-
Haplotype-resolved genome sequencing of a Gujarati Indian individual
-
Kitzman JO, MacKenzie AP, Adey A, Hiatt JB, Patwardhan RP, et al. 2011. Haplotype-resolved genome sequencing of a Gujarati Indian individual. Nat. Biotechnol. 29:59-63
-
(2011)
Nat. Biotechnol
, vol.29
, pp. 59-63
-
-
Kitzman, J.O.1
MacKenzie, A.P.2
Adey, A.3
Hiatt, J.B.4
Patwardhan, R.P.5
-
34
-
-
78049354879
-
Fine-scale recombination rate differences between sexes, populations and individuals
-
Kong A, ThorleifssonG,GudbjartssonDF, MassonG, SigurdssonA, et al. 2010. Fine-scale recombination rate differences between sexes, populations and individuals. Nature 467:1099-103
-
(2010)
Nature
, vol.467
, pp. 1099-1103
-
-
Kong, A.1
Thorleifsson, G.2
Gudbjartsson, D.F.3
Masson, G.4
Sigurdsson, A.5
-
35
-
-
84864394611
-
Genomic sequencing of unculturedmicroorganisms from single cells
-
Lasken RS. 2012. Genomic sequencing of unculturedmicroorganisms from single cells. Nat. Rev. Microbiol. 10:631-40
-
(2012)
Nat. Rev. Microbiol
, vol.10
, pp. 631-640
-
-
Lasken, R.S.1
-
36
-
-
84875160584
-
Single-cell sequencing in its prime
-
Lasken RS. 2013. Single-cell sequencing in its prime. Nat. Biotechnol. 31:211-12
-
(2013)
Nat. Biotechnol
, vol.31
, pp. 211-212
-
-
Lasken, R.S.1
-
37
-
-
0242475336
-
Whole genome amplification: Abundant supplies of DNA from precious samples or clinical specimens
-
Lasken RS, Egholm M. 2003. Whole genome amplification: abundant supplies of DNA from precious samples or clinical specimens. Trends Biotechnol. 21:531-35
-
(2003)
Trends Biotechnol
, vol.21
, pp. 531-535
-
-
Lasken, R.S.1
Egholm, M.2
-
38
-
-
35648976118
-
The diploid genome sequence of an individual human
-
Levy S, SuttonG,Ng PC, Feuk L, Halpern AL, et al. 2007. The diploid genome sequence of an individual human. PLOS Biol. 5:e254
-
(2007)
PLOS Biol
, vol.5
, pp. e254
-
-
Levy, S.1
Sutton, G.2
Ng, P.C.3
Feuk, L.4
Halpern, A.L.5
-
39
-
-
84900333051
-
Whole-exome sequencing of circulating tumor cells provides a window into metastatic prostate cancer
-
Lohr JG, Adalsteinsson VA, Cibulskis K, Choudhury AD, Rosenberg M, et al. 2014. Whole-exome sequencing of circulating tumor cells provides a window into metastatic prostate cancer. Nat. Biotechnol. 32:479-84
-
(2014)
Nat. Biotechnol
, vol.32
, pp. 479-484
-
-
Lohr, J.G.1
Adalsteinsson, V.A.2
Cibulskis, K.3
Choudhury, A.D.4
Rosenberg, M.5
-
40
-
-
84871447495
-
Probing meiotic recombination and aneuploidy of single sperm cells by whole-genome sequencing
-
Lu S, Zong C, Fan W, Yang M, Li J, et al. 2012. Probing meiotic recombination and aneuploidy of single sperm cells by whole-genome sequencing. Science 338:1627-30
-
(2012)
Science
, vol.338
, pp. 1627-1630
-
-
Lu, S.1
Zong, C.2
Fan, W.3
Yang, M.4
Li, J.5
-
41
-
-
77951652022
-
Direct determination of molecular haplotypes by chromosome microdissection
-
Ma L, Xiao Y, Huang H,Wang Q, Rao W, et al. 2010. Direct determination of molecular haplotypes by chromosome microdissection. Nat. Methods 7:299
-
(2010)
Nat. Methods
, vol.7
, pp. 299
-
-
Ma, L.1
Xiao, Y.2
Huang, H.3
Wang, Q.4
Rao, W.5
-
42
-
-
84864225382
-
Methods: Face up to false positives
-
MacArthur D. 2012. Methods: face up to false positives. Nature 487:427-28
-
(2012)
Nature
, vol.487
, pp. 427-428
-
-
MacArthur, D.1
-
43
-
-
24044455869
-
Genome sequencing in microfabricated high-density picolitre reactors
-
Margulies M, Egholm M, AltmanWE, Attiya S, Bader JS, et al. 2005. Genome sequencing in microfabricated high-density picolitre reactors. Nature 437:376-80
-
(2005)
Nature
, vol.437
, pp. 376-380
-
-
Margulies, M.1
Egholm, M.2
Altman, W.E.3
Attiya, S.4
Bader, J.S.5
-
44
-
-
4043128071
-
Genetic analysis of genome-wide variation in human gene expression
-
Morley M, Molony CM,Weber TM,Devlin JL, Ewens KG, et al. 2004. Genetic analysis of genome-wide variation in human gene expression. Nature 430:743-47
-
(2004)
Nature
, vol.430
, pp. 743-747
-
-
Morley, M.1
Molony, C.M.2
Weber, T.M.3
Devlin, J.L.4
Ewens, K.G.5
-
45
-
-
84940681987
-
-
Tech. Doc. , Sigma-Aldrich, St. Louis, MO
-
Mueller E, Brueck C. 2015. Whole genome amplification for single cell biology. Tech. Doc., Sigma-Aldrich, St. Louis, MO. http://www.sigmaaldrich.com/technical-documents/articles/life-science-innovations/ whole-genome-amplification.html
-
(2015)
Whole Genome Amplification for Single Cell Biology
-
-
Mueller, E.1
Brueck, C.2
-
46
-
-
84897141974
-
Method of the Year 2013
-
Nat. Methods
-
Nat. Methods Eds. 2014. Method of the Year 2013. Nat. Methods 11:1
-
(2014)
Nat. Methods
, vol.11
, pp. 1
-
-
-
47
-
-
85027920141
-
Cancer genomics: One cell at a time
-
Navin NE. 2014. Cancer genomics: one cell at a time. Genome Biol. 15:452
-
(2014)
Genome Biol
, vol.15
, pp. 452
-
-
Navin, N.E.1
-
48
-
-
79953766940
-
Tumour evolution inferred by single-cell sequencing
-
NavinNE, Kendall J, Troge J, Andrews P,Rodgers L, et al. 2011. Tumour evolution inferred by single-cell sequencing. Nature 472:90-94
-
(2011)
Nature
, vol.472
, pp. 90-94
-
-
Navin, N.E.1
Kendall, J.2
Troge, J.3
Andrews, P.4
Rodgers, L.5
-
49
-
-
84891354380
-
Reproducible copy number variation patterns among single circulating tumor cells of lung cancer patients
-
Ni X, Zhuo M, Su Z, Duan J, Gao Y, et al. 2013. Reproducible copy number variation patterns among single circulating tumor cells of lung cancer patients. PNAS 110:21083-88
-
(2013)
PNAS
, vol.110
, pp. 21083-21088
-
-
Ni, X.1
Zhuo, M.2
Su, Z.3
Duan, J.4
Gao, Y.5
-
50
-
-
84863637922
-
Accurate whole-genome sequencing and haplotyping from 10 to 20 human cells
-
Peters BA, Kermani BG, Sparks AB, Alferov O, Hong P, et al. 2012. Accurate whole-genome sequencing and haplotyping from 10 to 20 human cells. Nature 487:190-95
-
(2012)
Nature
, vol.487
, pp. 190-195
-
-
Peters, B.A.1
Kermani, B.G.2
Sparks, A.B.3
Alferov, O.4
Hong, P.5
-
51
-
-
48349105094
-
Impact of whole genome amplification on analysis of copy number variants
-
Pugh TJ, Delaney AD, Farnoud N, Flibotte S, Griffith M, et al. 2008. Impact of whole genome amplification on analysis of copy number variants. Nucleic Acids Res. 36:e80
-
(2008)
Nucleic Acids Res
, vol.36
, pp. e80
-
-
Pugh, T.J.1
Delaney, A.D.2
Farnoud, N.3
Flibotte, S.4
Griffith, M.5
-
52
-
-
84876412970
-
Use of array comparative genomic hybridization (array-CGH) for embryo assessment: Clinical results
-
Rubio C, Rodrigo L, Mir P, Mateu E, Peinado V, et al. 2013. Use of array comparative genomic hybridization (array-CGH) for embryo assessment: clinical results. Fertil. Steril. 99:1044-48
-
(2013)
Fertil. Steril
, vol.99
, pp. 1044-1048
-
-
Rubio, C.1
Rodrigo, L.2
Mir, P.3
Mateu, E.4
Peinado, V.5
-
53
-
-
84923351687
-
Limited genomic heterogeneity of circulating melanoma cells in advanced stage patients
-
Ruiz C, Li J, Luttgen MS, Kolatkar A, Kendall JT, et al. 2015. Limited genomic heterogeneity of circulating melanoma cells in advanced stage patients. Phys. Biol. 12:016008
-
(2015)
Phys. Biol
, vol.12
, pp. 016008
-
-
Ruiz, C.1
Li, J.2
Luttgen, M.S.3
Kolatkar, A.4
Kendall, J.T.5
-
54
-
-
0023850178
-
Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase
-
Saiki RK, Gelfand DH, Stoffel S, Scharf SJ, Higuchi R, et al. 1988. Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science 239:487-91
-
(1988)
Science
, vol.239
, pp. 487-491
-
-
Saiki, R.K.1
Gelfand, D.H.2
Stoffel, S.3
Scharf, S.J.4
Higuchi, R.5
-
55
-
-
84894630323
-
Entering the era of single-cell transcriptomics in biology and medicine
-
Sandberg R. 2014. Entering the era of single-cell transcriptomics in biology and medicine. Nat. Methods 11:22-24
-
(2014)
Nat. Methods
, vol.11
, pp. 22-24
-
-
Sandberg, R.1
-
56
-
-
3242808027
-
Large-scale copy number polymorphism in the human genome
-
Sebat J, Lakshmi B, Troge J, Alexander J, Young J, et al. 2004. Large-scale copy number polymorphism in the human genome. Science 305:525-28
-
(2004)
Science
, vol.305
, pp. 525-528
-
-
Sebat, J.1
Lakshmi, B.2
Troge, J.3
Alexander, J.4
Young, J.5
-
57
-
-
84882455458
-
Single-cell sequencing-based technologies will revolutionize whole-organism science
-
Shapiro E, Biezuner T, Linnarsson S. 2013. Single-cell sequencing-based technologies will revolutionize whole-organism science. Nat. Rev. Genet. 14:619-30
-
(2013)
Nat. Rev. Genet
, vol.14
, pp. 619-630
-
-
Shapiro, E.1
Biezuner, T.2
Linnarsson, S.3
-
58
-
-
84881133553
-
Successful PGD for late infantile neuronal ceroid lipofuscinosis achieved by combined chromosome and TPP1 gene analysis
-
Shen J, Cram DS, Wu W, Cai L, Yang X, et al. 2013. Successful PGD for late infantile neuronal ceroid lipofuscinosis achieved by combined chromosome and TPP1 gene analysis. Reprod. BioMed. Online 27:176-83
-
(2013)
Reprod. BioMed. Online
, vol.27
, pp. 176-183
-
-
Shen, J.1
Cram, D.S.2
Wu, W.3
Cai, L.4
Yang, X.5
-
59
-
-
80053028550
-
A comprehensively molecular haplotype-resolved genome of a European individual
-
Suk EK, McEwen GK, Duitama J, Nowick K, Schulz S, et al. 2011. A comprehensively molecular haplotype-resolved genome of a European individual. Genome Res. 21:1672-85
-
(2011)
Genome Res
, vol.21
, pp. 1672-1685
-
-
Suk, E.K.1
McEwen, G.K.2
Duitama, J.3
Nowick, K.4
Schulz, S.5
-
60
-
-
79953288433
-
Development and applications of single-cell transcriptome analysis
-
Tang F, Lao K, Surani MA. 2011. Development and applications of single-cell transcriptome analysis. Nat. Methods 8(Suppl.):S6-11
-
(2011)
Nat. Methods
, vol.8
, pp. S6-11
-
-
Tang, F.1
Lao, K.2
Surani, M.A.3
-
61
-
-
0026736251
-
Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer
-
Telenius H, Carter NP, Bebb CE, Nordenskjo M, Ponder BA, Tunnacliffe A. 1992. Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer. Genomics 13:718-25
-
(1992)
Genomics
, vol.13
, pp. 718-725
-
-
Telenius, H.1
Carter, N.P.2
Bebb, C.E.3
Nordenskjo, M.4
Ponder, B.A.5
Tunnacliffe, A.6
-
62
-
-
79951810290
-
The importance of phase information for human genomics
-
Tewhey R, Bansal V, Torkamani A, Topol EJ, Schork NJ. 2011. The importance of phase information for human genomics. Nat. Rev. Genet. 12:215-23
-
(2011)
Nat. Rev. Genet
, vol.12
, pp. 215-223
-
-
Tewhey, R.1
Bansal, V.2
Torkamani, A.3
Topol, E.J.4
Schork, N.J.5
-
63
-
-
84904381760
-
Two different microarray technologies for preimplantation genetic diagnosis and screening, due to reciprocal translocation imbalances, demonstrate equivalent euploidy and clinical pregnancy rates
-
Tobler KJ, Brezina PR, Benner AT, Du L, Xu X, Kearns WG. 2014. Two different microarray technologies for preimplantation genetic diagnosis and screening, due to reciprocal translocation imbalances, demonstrate equivalent euploidy and clinical pregnancy rates. J. Assist. Reprod. Genet. 31:843-50
-
(2014)
J. Assist. Reprod. Genet
, vol.31
, pp. 843-850
-
-
Tobler, K.J.1
Brezina, P.R.2
Benner, A.T.3
Du, L.4
Xu, X.5
Kearns, W.G.6
-
64
-
-
84875700912
-
Evaluation of targeted next-generation sequencing-based preimplantation genetic diagnosis of monogenic disease
-
TreffNR, Fedick A, Tao X,Devkota B,TaylorD, Scott RT. 2013. Evaluation of targeted next-generation sequencing-based preimplantation genetic diagnosis of monogenic disease. Fertil. Steril. 99:1377-84
-
(2013)
Fertil. Steril
, vol.99
, pp. 1377-1384
-
-
Treff, N.R.1
Fedick, A.2
Tao, X.3
Devkota, B.4
Taylor, D.5
Scott, R.T.6
-
65
-
-
84858380925
-
Development and validation of an accurate quantitative real-time polymerase chain reaction-based assay for human blastocyst comprehensive chromosomal aneuploidy screening
-
Treff NR, Tao X, Ferry KM, Su J, Taylor D, Scott RT. 2012. Development and validation of an accurate quantitative real-time polymerase chain reaction-based assay for human blastocyst comprehensive chromosomal aneuploidy screening. Fertil. Steril. 97:819-24
-
(2012)
Fertil. Steril
, vol.97
, pp. 819-824
-
-
Treff, N.R.1
Tao, X.2
Ferry, K.M.3
Su, J.4
Taylor, D.5
Scott, R.T.6
-
66
-
-
7044264544
-
Myosin binding protein Cmutations and compound heterozygosity in hypertrophic cardiomyopathy
-
Van Driest SL, Vasile VC, Ommen SR, Will ML, Tajik AJ, et al. 2004. Myosin binding protein Cmutations and compound heterozygosity in hypertrophic cardiomyopathy. J. Am. Coll. Cardiol. 44:1903-10
-
(2004)
J. Am. Coll. Cardiol
, vol.44
, pp. 1903-1910
-
-
Van Driest, S.L.1
Vasile, V.C.2
Ommen, S.R.3
Will, M.L.4
Tajik, A.J.5
-
67
-
-
4043181214
-
Cancer genes and the pathways they control
-
Vogelstein B, Kinzler KW. 2004. Cancer genes and the pathways they control. Nat. Med. 10:789-99
-
(2004)
Nat. Med
, vol.10
, pp. 789-799
-
-
Vogelstein, B.1
Kinzler, K.W.2
-
68
-
-
84864258558
-
Genome-wide single-cell analysis of recombination activity and de novo mutation rates in human sperm
-
Wang J, Fan HC, Behr B, Quake SR. 2012. Genome-wide single-cell analysis of recombination activity and de novo mutation rates in human sperm. Cell 150:402-12
-
(2012)
Cell
, vol.150
, pp. 402-412
-
-
Wang, J.1
Fan, H.C.2
Behr, B.3
Quake, S.R.4
-
69
-
-
55549097849
-
The diploid genome sequence of an Asian individual
-
Wang J, Wang W, Li R, Li Y, Tian G, 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
Wang, W.2
Li, R.3
Li, Y.4
Tian, G.5
-
70
-
-
84906238686
-
Clonal evolution in breast cancer revealed by single nucleus genome sequencing
-
Wang Y, Waters J, Leung ML, Unruh A, Roh W, et al. 2014. Clonal evolution in breast cancer revealed by single nucleus genome sequencing. Nature 512:155-60
-
(2014)
Nature
, vol.512
, pp. 155-160
-
-
Wang, Y.1
Waters, J.2
Leung, M.L.3
Unruh, A.4
Roh, W.5
-
71
-
-
84905487367
-
Clinical utilisation of a rapid low-pass whole genome sequencing technique for the diagnosis of aneuploidy in human embryos prior to implantation
-
Wells D, Kaur K, Grifo J,Glassner M, Taylor JC, et al. 2014. Clinical utilisation of a rapid low-pass whole genome sequencing technique for the diagnosis of aneuploidy in human embryos prior to implantation. J. Med. Genet. 51:553-62
-
(2014)
J. Med. Genet
, vol.51
, pp. 553-562
-
-
Wells, D.1
Kaur, K.2
Grifo, J.3
Glassner, M.4
Taylor, J.C.5
-
72
-
-
42249087308
-
The complete genome of an individual by massively parallel DNA sequencing
-
Wheeler DA, Srinivasan M, Egholm M, Shen Y, Chen L, et al. 2008. The complete genome of an individual by massively parallel DNA sequencing. Nature 452:872-76
-
(2008)
Nature
, vol.452
, pp. 872-876
-
-
Wheeler, D.A.1
Srinivasan, M.2
Egholm, M.3
Shen, Y.4
Chen, L.5
-
73
-
-
84863230091
-
Single-cell exome sequencing reveals single-nucleotide mutation characteristics of a kidney tumor
-
Xu X, Hou Y, Yin X, Bao L, Tang A, et al. 2012. Single-cell exome sequencing reveals single-nucleotide mutation characteristics of a kidney tumor. Cell 148:886-95
-
(2012)
Cell
, vol.148
, pp. 886-895
-
-
Xu, X.1
Hou, Y.2
Yin, X.3
Bao, L.4
Tang, A.5
-
74
-
-
78651109312
-
Completely phased genome sequencing through chromosome sorting
-
Yang H, Chen X,WongWH.2011. Completely phased genome sequencing through chromosome sorting. PNAS 108:12-17
-
(2011)
PNAS
, vol.108
, pp. 12-17
-
-
Yang, H.1
Chen, X.2
Wong, W.H.3
-
75
-
-
84901835055
-
Discovery of biclonal origin and a novel oncogene SLC12A5 in colon cancer by single-cell sequencing
-
Yu C, Yu J, YaoX,WuWK, Lu Y, et al. 2014. Discovery of biclonal origin and a novel oncogene SLC12A5 in colon cancer by single-cell sequencing. Cell Res. 24:701-12
-
(2014)
Cell Res
, vol.24
, pp. 701-712
-
-
Yu, C.1
Yu, J.2
Yao, X.3
Wu, W.K.4
Lu, Y.5
-
76
-
-
33644627112
-
Long-range polony haplotyping of individual human chromosome molecules
-
ZhangK,Zhu J, Shendure J,Porreca GJ, Aach JD, et al. 2006. Long-range polony haplotyping of individual human chromosome molecules. Nat. Genet. 38:382-87
-
(2006)
Nat. Genet
, vol.38
, pp. 382-387
-
-
Zhang, K.1
Zhu, J.2
Shendure, J.3
Porreca, G.J.4
Aach, J.D.5
-
77
-
-
0026755807
-
Whole genome amplification from a single cell: Implications for genetic analysis
-
Zhang L, Cui X, Schmitt K, Hubert R, Navidi W, Arnheim N. 1992. Whole genome amplification from a single cell: implications for genetic analysis. PNAS 89:5847-51
-
(1992)
PNAS
, vol.89
, pp. 5847-5851
-
-
Zhang, L.1
Cui, X.2
Schmitt, K.3
Hubert, R.4
Navidi, W.5
Arnheim, N.6
-
78
-
-
84871461434
-
Genome-wide detection of single-nucleotide and copy-number variations of a single human cell
-
ZongC,Lu S,Chapman AR,Xie XS. 2012. Genome-wide detection of single-nucleotide and copy-number variations of a single human cell. Science 338:1622-26
-
(2012)
Science
, vol.338
, pp. 1622-1626
-
-
Zong, C.1
Lu, S.2
Chapman, A.R.3
Xie, X.S.4
|