-
1
-
-
33747195353
-
Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors
-
Takahashi, K. & Yamanaka, S. Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors. Cell 126, 663-676 (2006).
-
(2006)
Cell
, vol.126
, pp. 663-676
-
-
Takahashi, K.1
Yamanaka, S.2
-
2
-
-
36248966518
-
Induction of pluripotent stem cells from adult human fibroblasts by defined factors
-
Takahashi, K. et al. Induction of pluripotent stem cells from adult human fibroblasts by defined factors. Cell 131, 861-872 (2007).
-
(2007)
Cell
, vol.131
, pp. 861-872
-
-
Takahashi, K.1
-
3
-
-
50549089957
-
Disease-specific induced pluripotent stem cells
-
Park, I. H. et al. Disease-specific induced pluripotent stem cells. Cell 134, 877-886 (2008).
-
(2008)
Cell
, vol.134
, pp. 877-886
-
-
Park, I.H.1
-
4
-
-
61349100729
-
Parkinson's Disease patient-derived induced pluripotent stem cells free of viral reprogramming factors
-
Soldner, F. et al. Parkinson's Disease patient-derived induced pluripotent stem cells free of viral reprogramming factors. Cell 136, 964-977 (2009).
-
(2009)
Cell
, vol.136
, pp. 964-977
-
-
Soldner, F.1
-
5
-
-
84881184980
-
Vascularized and functional human liver from an iPSC-derived organ bud transplant
-
Takebe, T. et al. Vascularized and functional human liver from an iPSC-derived organ bud transplant. Nature 499, 481-484 (2013).
-
(2013)
Nature
, vol.499
, pp. 481-484
-
-
Takebe, T.1
-
6
-
-
63049090064
-
A fresh look at iPS cells
-
Yamanaka, S. A fresh look at iPS cells. Cell 137, 13-17 (2009).
-
(2009)
Cell
, vol.137
, pp. 13-17
-
-
Yamanaka, S.1
-
7
-
-
84881256653
-
Pluripotent stem cells induced from mouse somatic cells by smallmolecule compounds
-
Hou, P. et al. Pluripotent stem cells induced from mouse somatic cells by smallmolecule compounds. Science 341, 651-654 (2013).
-
(2013)
Science
, vol.341
, pp. 651-654
-
-
Hou, P.1
-
8
-
-
0032509440
-
Eight calves cloned from somatic cells of a single adult
-
Kato, Y. et al. Eight calves cloned from somatic cells of a single adult. Science 282, 2095-2098 (1998).
-
(1998)
Science
, vol.282
, pp. 2095-2098
-
-
Kato, Y.1
-
9
-
-
0032560827
-
Full-term development of mice from enucleated oocytes injected with cumulus cell nuclei
-
Wakayama, T., Perry, A. C., Zuccotti, M., Johnson, K. R. & Yanagimachi, R. Full-term development of mice from enucleated oocytes injected with cumulus cell nuclei. Nature 394, 369-374 (1998).
-
(1998)
Nature
, vol.394
, pp. 369-374
-
-
Wakayama, T.1
Perry, A.C.2
Zuccotti, M.3
Johnson, K.R.4
Yanagimachi, R.5
-
10
-
-
0031044215
-
Viable offspring derived from fetal and adult mammalian cells
-
Wilmut, I., Schnieke, A. E., McWhir, J., Kind, A. J. & Campbell, K. H. Viable offspring derived from fetal and adult mammalian cells. Nature 385, 810-813 (1997).
-
(1997)
Nature
, vol.385
, pp. 810-813
-
-
Wilmut, I.1
Schnieke, A.E.2
McWhir, J.3
Kind, A.J.4
Campbell, K.H.5
-
11
-
-
36749043230
-
Induced pluripotent stem cell lines derived from human somatic cells
-
Yu, J. et al. Induced pluripotent stem cell lines derived from human somatic cells. Science 318, 1917-1920 (2007).
-
(2007)
Science
, vol.318
, pp. 1917-1920
-
-
Yu, J.1
-
12
-
-
84875153918
-
Successful serial recloning in the mouse over multiple generations
-
Wakayama, S. et al. Successful serial recloning in the mouse over multiple generations. Cell Stem Cell 12, 293-297 (2013).
-
(2013)
Cell Stem Cell
, vol.12
, pp. 293-297
-
-
Wakayama, S.1
-
13
-
-
69949104478
-
Adult mice generated from induced pluripotent stem cells
-
Boland, M. J. et al. Adult mice generated from induced pluripotent stem cells. Nature 461, 91-94 (2009).
-
(2009)
Nature
, vol.461
, pp. 91-94
-
-
Boland, M.J.1
-
14
-
-
82755185948
-
Reprogramming factor stoichiometry influences the epigenetic state and biological properties of induced pluripotent stem cells
-
Carey, B. W. et al. Reprogramming factor stoichiometry influences the epigenetic state and biological properties of induced pluripotent stem cells. Cell Stem Cell 9, 588-598 (2011).
-
(2011)
Cell Stem Cell
, vol.9
, pp. 588-598
-
-
Carey, B.W.1
-
15
-
-
67849133023
-
IPS cells can support full-term development of tetraploid blastocyst-complemented embryos
-
Kang, L., Wang, J. L., Zhang, Y., Kou, Z. H. & Gao, S. R. iPS cells can support full-term development of tetraploid blastocyst-complemented embryos. Cell Stem Cell 5, 135-138 (2009).
-
(2009)
Cell Stem Cell
, vol.5
, pp. 135-138
-
-
Kang, L.1
Wang, J.L.2
Zhang, Y.3
Kou, Z.H.4
Gao, S.R.5
-
16
-
-
77952425747
-
Aberrant silencing of imprinted genes on chromosome 12qF1 in mouse induced pluripotent stem cells
-
Stadtfeld, M. et al. Aberrant silencing of imprinted genes on chromosome 12qF1 in mouse induced pluripotent stem cells. Nature 465, 175-181 (2010).
-
(2010)
Nature
, vol.465
, pp. 175-181
-
-
Stadtfeld, M.1
-
17
-
-
84860644898
-
Background mutations in parental cells account for most of the genetic heterogeneity of induced pluripotent stem cells
-
Young, M. A. et al. Background mutations in parental cells account for most of the genetic heterogeneity of induced pluripotent stem cells. Cell Stem Cell 10, 570-582 (2012).
-
(2012)
Cell Stem Cell
, vol.10
, pp. 570-582
-
-
Young, M.A.1
-
18
-
-
78650971216
-
Dynamic changes in the copy number of pluripotency and cell proliferation genes in human escs and ipscs during reprogramming and time in culture
-
Laurent, L. C. et al. Dynamic changes in the copy number of pluripotency and cell proliferation genes in human escs and ipscs during reprogramming and time in culture. Cell Stem Cell 8, 106-118 (2011).
-
(2011)
Cell Stem Cell
, vol.8
, pp. 106-118
-
-
Laurent, L.C.1
-
19
-
-
79952258224
-
Somatic coding mutations in human induced pluripotent stem cells
-
Gore, A. et al. Somatic coding mutations in human induced pluripotent stem cells. Nature 471, 63-76 (2011).
-
(2011)
Nature
, vol.471
, pp. 63-76
-
-
Gore, A.1
-
20
-
-
79952126043
-
Copy number variation and selection during reprogramming to pluripotency
-
Hussein, S. M. et al. Copy number variation and selection during reprogramming to pluripotency. Nature 471, 58-67 (2011).
-
(2011)
Nature
, vol.471
, pp. 58-67
-
-
Hussein, S.M.1
-
21
-
-
84857496469
-
Elevated coding mutation rate during the reprogramming of human somatic cells into induced pluripotent stem cells
-
Ji, J. F. et al. Elevated coding mutation rate during the reprogramming of human somatic cells into induced pluripotent stem cells. Stem Cells 30, 435-440 (2012).
-
(2012)
Stem Cells
, vol.30
, pp. 435-440
-
-
Ji, J.F.1
-
22
-
-
0034699380
-
Ageing: Cloning of mice to six generations
-
Wakayama, T. et al. Ageing: cloning of mice to six generations. Nature 407, 318-319 (2000).
-
(2000)
Nature
, vol.407
, pp. 318-319
-
-
Wakayama, T.1
-
23
-
-
77955060114
-
Mice cloned from induced pluripotent stem cells (iPSCs)
-
Kou, Z. H. et al. Mice cloned from induced pluripotent stem cells (iPSCs). Biol. Reprod. 83, 238-243 (2010).
-
(2010)
Biol. Reprod.
, vol.83
, pp. 238-243
-
-
Kou, Z.H.1
-
24
-
-
84897655065
-
High-throughput sequencing reveals the disruption of methylation of imprinted gene in induced pluripotent stem cells
-
Chang, G. et al. High-throughput sequencing reveals the disruption of methylation of imprinted gene in induced pluripotent stem cells. Cell Res. 24, 293-306 (2014).
-
(2014)
Cell Res.
, vol.24
, pp. 293-306
-
-
Chang, G.1
-
25
-
-
84859727275
-
The Mouse Genome Database (MGD): Comprehensive resource for genetics and genomics of the laboratory mouse
-
Eppig, J. T. et al. The Mouse Genome Database (MGD): comprehensive resource for genetics and genomics of the laboratory mouse. Nucleic Acids Res. 40, 881-886 (2012).
-
(2012)
Nucleic Acids Res.
, vol.40
, pp. 881-886
-
-
Eppig, J.T.1
-
26
-
-
20144386935
-
Genetic heterogeneity in Rubinstein-Taybi syndrome: Mutations in both the CBP and EP300 genes cause disease
-
Roelfsema, J. H. et al. Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease. Am. J. Hum. Genet. 76, 572-580 (2005).
-
(2005)
Am. J. Hum. Genet.
, vol.76
, pp. 572-580
-
-
Roelfsema, J.H.1
-
27
-
-
84870532434
-
Exome sequencing of serous endometrial tumors identifies recurrent somatic mutations in chromatin-remodeling and ubiquitin ligase complex genes
-
Le Gallo, M. et al. Exome sequencing of serous endometrial tumors identifies recurrent somatic mutations in chromatin-remodeling and ubiquitin ligase complex genes. Nat. Genet. 44, 1310-1315 (2012).
-
(2012)
Nat. Genet.
, vol.44
, pp. 1310-1315
-
-
Le Gallo, M.1
-
28
-
-
84866851740
-
Integrative genome analyses identify key somatic driver mutations of small-cell lung cancer
-
Peifer, M. et al. Integrative genome analyses identify key somatic driver mutations of small-cell lung cancer. Nat. Genet. 44, 1104-1110 (2012).
-
(2012)
Nat. Genet.
, vol.44
, pp. 1104-1110
-
-
Peifer, M.1
-
29
-
-
34547169962
-
Confirmation of EP300 gene mutations as a rare cause of Rubinstein-Taybi syndrome
-
Zimmermann, N., Acosta, A. M., Kohlhase, J. & Bartsch, O. Confirmation of EP300 gene mutations as a rare cause of Rubinstein-Taybi syndrome. Eur. J. Hum. Genet. 15, 837-842 (2007).
-
(2007)
Eur. J. Hum. Genet.
, vol.15
, pp. 837-842
-
-
Zimmermann, N.1
Acosta, A.M.2
Kohlhase, J.3
Bartsch, O.4
-
30
-
-
66849111902
-
Further case of Rubinstein-Taybi syndrome due to a deletion in EP300
-
Foley, P., Bunyan, D., Stratton, J., Dillon, M. & Lynch, S. A. Further case of Rubinstein-Taybi syndrome due to a deletion in EP300. Am. J. Med. Genet. A 149A, 997-1000 (2009).
-
(2009)
Am. J. Med. Genet. A
, vol.149 A
, pp. 997-1000
-
-
Foley, P.1
Bunyan, D.2
Stratton, J.3
Dillon, M.4
Lynch, S.A.5
-
31
-
-
75149162868
-
Two patients with EP300 mutations and facial dysmorphism different from the classic Rubinstein-Taybi syndrome
-
Bartsch, O. et al. Two patients with EP300 mutations and facial dysmorphism different from the classic Rubinstein-Taybi syndrome. Am. J. Med. Genet. A 152A, 181-184 (2010).
-
(2010)
Am. J. Med. Genet. A
, vol.152 A
, pp. 181-184
-
-
Bartsch, O.1
-
32
-
-
17644445419
-
Gene dosage-dependent embryonic development and proliferation defects in mice lacking the transcriptional integrator p300
-
Yao, T. P. et al. Gene dosage-dependent embryonic development and proliferation defects in mice lacking the transcriptional integrator p300. Cell 93, 361-372 (1998).
-
(1998)
Cell
, vol.93
, pp. 361-372
-
-
Yao, T.P.1
-
33
-
-
34548303921
-
Allelic variation in GAD1 (GAD(67)) is associated with schizophrenia and influences cortical function and gene expression
-
Straub, R. E. et al. Allelic variation in GAD1 (GAD(67)) is associated with schizophrenia and influences cortical function and gene expression. Mol. Psychiatry 12, 854-869 (2007).
-
(2007)
Mol. Psychiatry
, vol.12
, pp. 854-869
-
-
Straub, R.E.1
-
34
-
-
0035969990
-
Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia
-
Laitinen, P. J. et al. Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia. Circulation 103, 485-490 (2001).
-
(2001)
Circulation
, vol.103
, pp. 485-490
-
-
Laitinen, P.J.1
-
35
-
-
0035895322
-
Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia
-
Priori, S. G. et al. Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia. Circulation 103, 196-200 (2001).
-
(2001)
Circulation
, vol.103
, pp. 196-200
-
-
Priori, S.G.1
-
36
-
-
0035253502
-
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)
-
Tiso, N. et al. Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2). Hum. Mol. Genet. 10, 189-194 (2001).
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 189-194
-
-
Tiso, N.1
-
37
-
-
33747072861
-
Mice with the R176Q cardiac ryanodine receptor mutation exhibit catecholamine-induced ventricular tachycardia and cardiomyopathy
-
Kannankeril, P. J. et al. Mice with the R176Q cardiac ryanodine receptor mutation exhibit catecholamine-induced ventricular tachycardia and cardiomyopathy. Proc. Natl Acad. Sci. USA 103, 12179-12184 (2006).
-
(2006)
Proc. Natl Acad. Sci. USA
, vol.103
, pp. 12179-12184
-
-
Kannankeril, P.J.1
-
38
-
-
45749100010
-
Leaky Ca(2\+) release channel/ryanodine receptor 2 causes seizures and sudden cardiac death in mice
-
Lehnart, S. E. et al. Leaky Ca(2\+) release channel/ryanodine receptor 2 causes seizures and sudden cardiac death in mice. J. Clin. Invest. 118, 2230-2245 (2008).
-
(2008)
J. Clin. Invest.
, vol.118
, pp. 2230-2245
-
-
Lehnart, S.E.1
-
39
-
-
34848928486
-
Expanding spectrum of human RYR2-related disease: New electrocardiographic, structural, and genetic features
-
Bhuiyan, Z. A. et al. Expanding spectrum of human RYR2-related disease: new electrocardiographic, structural, and genetic features. Circulation 116, 1569-1576 (2007).
-
(2007)
Circulation
, vol.116
, pp. 1569-1576
-
-
Bhuiyan, Z.A.1
-
40
-
-
83155175187
-
Ryanodine receptor type 2 is required for the development of pressure overload-induced cardiac hypertrophy
-
Zou, Y. Z. et al. Ryanodine receptor type 2 is required for the development of pressure overload-induced cardiac hypertrophy. Hypertension 58, 1099-1110 (2011).
-
(2011)
Hypertension
, vol.58
, pp. 1099-1110
-
-
Zou, Y.Z.1
-
41
-
-
67651091685
-
CD2AP mutations are associated with sporadic nephrotic syndrome and focal segmental glomerulosclerosis (FSGS)
-
Gigante, M. et al. CD2AP mutations are associated with sporadic nephrotic syndrome and focal segmental glomerulosclerosis (FSGS). Nephrol. Dial. Transplant. 24, 1858-1864 (2009).
-
(2009)
Nephrol. Dial. Transplant.
, vol.24
, pp. 1858-1864
-
-
Gigante, M.1
-
42
-
-
77950353855
-
Analysis of recessive CD2AP and ACTN4 mutations in steroidresistant nephrotic syndrome
-
Benoit, G. et al. Analysis of recessive CD2AP and ACTN4 mutations in steroidresistant nephrotic syndrome. Pediatr. Nephrol. 25, 445-451 (2010).
-
(2010)
Pediatr. Nephrol.
, vol.25
, pp. 445-451
-
-
Benoit, G.1
-
43
-
-
0038136885
-
CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility
-
Kim, J. M. et al. CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility. Science 300, 1298-1300 (2003).
-
(2003)
Science
, vol.300
, pp. 1298-1300
-
-
Kim, J.M.1
-
44
-
-
33845387882
-
A novel compound heterozygous mutation in the DAP12 gene in a patient with Nasu-Hakola disease
-
Kuroda, R. et al. A novel compound heterozygous mutation in the DAP12 gene in a patient with Nasu-Hakola disease. J. Neurol. Sci. 252, 88-91 (2007).
-
(2007)
J. Neurol. Sci.
, vol.252
, pp. 88-91
-
-
Kuroda, R.1
-
45
-
-
84879684377
-
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1
-
Carvill, G. L. et al. Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1. Nat. Genet. 45, 825-830 (2013).
-
(2013)
Nat. Genet.
, vol.45
, pp. 825-830
-
-
Carvill, G.L.1
-
46
-
-
84899753582
-
CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems
-
Chenier, S. et al. CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems. J. Neurodev. Disord. 6, 9 (2014).
-
(2014)
J. Neurodev. Disord.
, vol.6
, pp. 9
-
-
Chenier, S.1
-
47
-
-
84871410004
-
Somatic copy number mosaicism in human skin revealed by induced pluripotent stem cells
-
Abyzov, A. et al. Somatic copy number mosaicism in human skin revealed by induced pluripotent stem cells. Nature 492, 438-442 (2012).
-
(2012)
Nature
, vol.492
, pp. 438-442
-
-
Abyzov, A.1
-
48
-
-
84855982119
-
Evaluation of a droplet digital polymerase chain reaction format for DNA copy number quantification
-
Pinheiro, L. B. et al. Evaluation of a droplet digital polymerase chain reaction format for DNA copy number quantification. Anal. Chem. 84, 1003-1011 (2012).
-
(2012)
Anal. Chem.
, vol.84
, pp. 1003-1011
-
-
Pinheiro, L.B.1
-
49
-
-
53549118586
-
Global organization of replication time zones of the mouse genome
-
Farkash-Amar, S. et al. Global organization of replication time zones of the mouse genome. Genome Res. 18, 1562-1570 (2008).
-
(2008)
Genome Res.
, vol.18
, pp. 1562-1570
-
-
Farkash-Amar, S.1
-
50
-
-
54949085778
-
Global reorganization of replication domains during embryonic stem cell differentiation
-
Hiratani, I. et al. Global reorganization of replication domains during embryonic stem cell differentiation. PLoS Biol. 6, 2220-2236 (2008).
-
(2008)
PLoS Biol.
, vol.6
, pp. 2220-2236
-
-
Hiratani, I.1
-
51
-
-
84898041397
-
The distribution of genomic variations in human iPSCs is related to replication-timing reorganization during reprogramming
-
Lu, J. et al. The distribution of genomic variations in human iPSCs is related to replication-timing reorganization during reprogramming. Cell Rep. 7, 70-78 (2014).
-
(2014)
Cell Rep.
, vol.7
, pp. 70-78
-
-
Lu, J.1
-
52
-
-
84871447495
-
Probing meiotic recombination and aneuploidy of single sperm cells by whole-genome sequencing
-
Lu, S. J. et al. Probing meiotic recombination and aneuploidy of single sperm cells by whole-genome sequencing. Science 338, 1627-1630 (2012).
-
(2012)
Science
, vol.338
, pp. 1627-1630
-
-
Lu, S.J.1
-
53
-
-
84871461434
-
Genome-wide detection of single-nucleotide and copy-number variations of a single human cell
-
Zong, C. H., Lu, S. J., Chapman, A. R. & Xie, X. S. Genome-wide detection of single-nucleotide and copy-number variations of a single human cell. Science 338, 1622-1626 (2012).
-
(2012)
Science
, vol.338
, pp. 1622-1626
-
-
Zong, C.H.1
Lu, S.J.2
Chapman, A.R.3
Xie, X.S.4
-
54
-
-
84863229606
-
Low incidence of DNA sequence variation in human induced pluripotent stem cells generated by nonintegrating plasmid expression
-
Cheng, L. Z. et al. Low incidence of DNA sequence variation in human induced pluripotent stem cells generated by nonintegrating plasmid expression. Cell Stem Cell 10, 337-344 (2012).
-
(2012)
Cell Stem Cell
, vol.10
, pp. 337-344
-
-
Cheng, L.Z.1
-
55
-
-
80053913326
-
Genome sequencing of mouse induced pluripotent stem cells reveals retroelement stability and infrequent DNA rearrangement during reprogramming
-
Quinlan, A. R. et al. Genome sequencing of mouse induced pluripotent stem cells reveals retroelement stability and infrequent DNA rearrangement during reprogramming. Cell Stem Cell 9, 366-373 (2011).
-
(2011)
Cell Stem Cell
, vol.9
, pp. 366-373
-
-
Quinlan, A.R.1
-
56
-
-
79958109873
-
Recurrent copy number variations in human induced pluripotent stem cells
-
Martins-Taylor, K. et al. Recurrent copy number variations in human induced pluripotent stem cells. Nat. Biotechnol. 29, 488-491 (2011).
-
(2011)
Nat. Biotechnol.
, vol.29
, pp. 488-491
-
-
Martins-Taylor, K.1
-
57
-
-
84878226536
-
Origins and implications of pluripotent stem cell variability and heterogeneity
-
Cahan, P. & Daley, G. Q. Origins and implications of pluripotent stem cell variability and heterogeneity. Nat. Rev. Mol. Cell Biol. 14, 357-368 (2013).
-
(2013)
Nat. Rev. Mol. Cell Biol.
, vol.14
, pp. 357-368
-
-
Cahan, P.1
Daley, G.Q.2
-
58
-
-
84887304781
-
Condensin II subunit dCAP-D3 restricts retrotransposon mobilization in Drosophila somatic cells
-
Schuster, A. T., Sarvepalli, K., Murphy, E. A. & Longworth, M. S. Condensin II subunit dCAP-D3 restricts retrotransposon mobilization in Drosophila somatic cells. PLoS Genet. 9, e1003879 (2013).
-
(2013)
PLoS Genet.
, vol.9
, pp. e1003879
-
-
Schuster, A.T.1
Sarvepalli, K.2
Murphy, E.A.3
Longworth, M.S.4
-
59
-
-
33746728798
-
Mouse adipose-derived stem cells undergo multilineage differentiation in vitro but primarily osteogenic and chondrogenic differentiation in vivo
-
Zheng, B., Cao, B. H., Li, G. H. & Huard, J. Mouse adipose-derived stem cells undergo multilineage differentiation in vitro but primarily osteogenic and chondrogenic differentiation in vivo. Tiss. Eng. 12, 1891-1901 (2006).
-
(2006)
Tiss. Eng.
, vol.12
, pp. 1891-1901
-
-
Zheng, B.1
Cao, B.H.2
Li, G.H.3
Huard, J.4
-
60
-
-
77949587649
-
And accurate long-read alignment with Burrows-Wheeler transform
-
Li, H. & Durbin, R. Fast and accurate long-read alignment with Burrows-Wheeler transform. Bioinformatics 26, 589-595 (2010).
-
(2010)
Bioinformatics
, vol.26
, pp. 589-595
-
-
Li, H.1
Fast, D.R.2
-
61
-
-
53849146020
-
Model-based analysis of ChIP-Seq (MACS)
-
Zhang, Y. et al. Model-based analysis of ChIP-Seq (MACS). Genome Biol. 9, R137 (2008).
-
(2008)
Genome Biol.
, vol.9
, pp. R137
-
-
Zhang, Y.1
-
62
-
-
65449136284
-
TopHat: Discovering splice junctions with RNA-Seq
-
Trapnell, C., Pachter, L. & Salzberg, S. L. TopHat: discovering splice junctions with RNA-Seq. Bioinformatics 25, 1105-1111 (2009).
-
(2009)
Bioinformatics
, vol.25
, pp. 1105-1111
-
-
Trapnell, C.1
Pachter, L.2
Salzberg, S.L.3
-
63
-
-
80051941094
-
Identification of novel transcripts in annotated genomes using RNA-Seq
-
Roberts, A., Pimentel, H., Trapnell, C. & Pachter, L. Identification of novel transcripts in annotated genomes using RNA-Seq. Bioinformatics 27, 2325-2329 (2011).
-
(2011)
Bioinformatics
, vol.27
, pp. 2325-2329
-
-
Roberts, A.1
Pimentel, H.2
Trapnell, C.3
Pachter, L.4
-
64
-
-
68549104404
-
The sequence alignment/map format and SAMtools
-
Li, H. et al. The sequence alignment/map format and SAMtools. Bioinformatics 25, 2078-2079 (2009).
-
(2009)
Bioinformatics
, vol.25
, pp. 2078-2079
-
-
Li, H.1
-
65
-
-
0033621054
-
Chip-based genotyping by mass spectrometry
-
Tang, K. et al. Chip-based genotyping by mass spectrometry. Proc. Natl Acad. Sci. USA 96, 10016-10020 (1999).
-
(1999)
Proc. Natl Acad. Sci. USA
, vol.96
, pp. 10016-10020
-
-
Tang, K.1
-
66
-
-
79951970227
-
An approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing
-
Abyzov, A., Urban, A. E., Snyder, M. & Gerstein, M. CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing. Genome Res. 21, 974-984 (2011).
-
(2011)
Genome Res.
, vol.21
, pp. 974-984
-
-
Abyzov, A.1
Urban, A.E.2
Snyder, M.3
Cnvnator, G.M.4
-
67
-
-
69549116107
-
BreakDancer: An algorithm for high-resolution mapping of genomic structural variation
-
Chen, K. et al. BreakDancer: an algorithm for high-resolution mapping of genomic structural variation. Nat. Methods 6, 677-681 (2009).
-
(2009)
Nat. Methods
, vol.6
, pp. 677-681
-
-
Chen, K.1
|