-
2
-
-
3543110316
-
Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of down syndrome
-
Kahlem P, Sultan M, Herwig R, Steinfath M, Balzereit D, et al. (2004) Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of down syndrome. Genome Res 14: 1258-1267.
-
(2004)
Genome Res
, vol.14
, pp. 1258-1267
-
-
Kahlem, P.1
Sultan, M.2
Herwig, R.3
Steinfath, M.4
Balzereit, D.5
-
3
-
-
3543097554
-
Gene expression from the aneuploid chromosome in a trisomy mouse model of down syndrome
-
Lyle R, Gehrig C, Neergaard-Henrichsen C, Deutsch S, Antonarakis SE, (2004) Gene expression from the aneuploid chromosome in a trisomy mouse model of down syndrome. Genome Res 14: 1268-1274.
-
(2004)
Genome Res
, vol.14
, pp. 1268-1274
-
-
Lyle, R.1
Gehrig, C.2
Neergaard-Henrichsen, C.3
Deutsch, S.4
Antonarakis, S.E.5
-
4
-
-
0037403505
-
Global up-regulation of chromosome 21 gene expression in the developing Down syndrome brain
-
Mao R, Zielke CL, Zielke HR, Pevsner J, (2003) Global up-regulation of chromosome 21 gene expression in the developing Down syndrome brain. Genomics 81: 457-467.
-
(2003)
Genomics
, vol.81
, pp. 457-467
-
-
Mao, R.1
Zielke, C.L.2
Zielke, H.R.3
Pevsner, J.4
-
5
-
-
0037115492
-
Transcriptome analysis of human autosomal trisomy
-
FitzPatrick DR, Ramsay J, McGill NI, Shade M, Carothers AD, et al. (2002) Transcriptome analysis of human autosomal trisomy. Hum Mol Genet 11: 3249-3256.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 3249-3256
-
-
FitzPatrick, D.R.1
Ramsay, J.2
McGill, N.I.3
Shade, M.4
Carothers, A.D.5
-
6
-
-
79955399112
-
Massive-scale RNA-Seq analysis of non ribosomal transcriptome in human trisomy 21
-
Costa V, Angelini C, D'Apice L, Mutarelli M, Casamassimi A, et al. (2011) Massive-scale RNA-Seq analysis of non ribosomal transcriptome in human trisomy 21. PLoS One 6: e18493.
-
(2011)
PLoS One
, vol.6
-
-
Costa, V.1
Angelini, C.2
D'Apice, L.3
Mutarelli, M.4
Casamassimi, A.5
-
7
-
-
34548084502
-
Genome-wide expression analysis of cultured trophoblast with trisomy 21 karyotype
-
Rozovski U, Jonish-Grossman A, Bar-Shira A, Ochshorn Y, Goldstein M, et al. (2007) Genome-wide expression analysis of cultured trophoblast with trisomy 21 karyotype. Hum Reprod 22: 2538-2545.
-
(2007)
Hum Reprod
, vol.22
, pp. 2538-2545
-
-
Rozovski, U.1
Jonish-Grossman, A.2
Bar-Shira, A.3
Ochshorn, Y.4
Goldstein, M.5
-
8
-
-
77950187447
-
Dnmt1 and Dnmt3a maintain DNA methylation and regulate synaptic function in adult forebrain neurons
-
Feng J, Zhou Y, Campbell SL, Le T, Li E, et al. (2010) Dnmt1 and Dnmt3a maintain DNA methylation and regulate synaptic function in adult forebrain neurons. Nat Neurosci 13: 423-430.
-
(2010)
Nat Neurosci
, vol.13
, pp. 423-430
-
-
Feng, J.1
Zhou, Y.2
Campbell, S.L.3
Le, T.4
Li, E.5
-
9
-
-
79955538247
-
Hydroxylation of 5-methylcytosine by TET1 promotes active DNA demethylation in the adult brain
-
Guo JU, Su Y, Zhong C, Ming GL, Song H, (2011) Hydroxylation of 5-methylcytosine by TET1 promotes active DNA demethylation in the adult brain. Cell 145: 423-434.
-
(2011)
Cell
, vol.145
, pp. 423-434
-
-
Guo, J.U.1
Su, Y.2
Zhong, C.3
Ming, G.L.4
Song, H.5
-
11
-
-
0032830639
-
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
-
Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, et al. (1999) Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet 23: 185-188.
-
(1999)
Nat Genet
, vol.23
, pp. 185-188
-
-
Amir, R.E.1
van den Veyver, I.B.2
Wan, M.3
Tran, C.Q.4
Francke, U.5
-
12
-
-
13844321733
-
In psychosis, cortical interneurons overexpress DNA-methyltransferase 1
-
Veldic M, Guidotti A, Maloku E, Davis JM, Costa E, (2005) In psychosis, cortical interneurons overexpress DNA-methyltransferase 1. Proc Natl Acad Sci U S A 102: 2152-2157.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 2152-2157
-
-
Veldic, M.1
Guidotti, A.2
Maloku, E.3
Davis, J.M.4
Costa, E.5
-
13
-
-
70350512022
-
Function and regulation of Dyrk1A: towards understanding Down syndrome
-
Park J, Song WJ, Chung KC, (2009) Function and regulation of Dyrk1A: towards understanding Down syndrome. Cell Mol Life Sci 66: 3235-3240.
-
(2009)
Cell Mol Life Sci
, vol.66
, pp. 3235-3240
-
-
Park, J.1
Song, W.J.2
Chung, K.C.3
-
14
-
-
0034969415
-
Homocysteine metabolism in children with Down syndrome: in vitro modulation
-
Pogribna M, Melnyk S, Pogribny I, Chango A, Yi P, et al. (2001) Homocysteine metabolism in children with Down syndrome: in vitro modulation. Am J Hum Genet 69: 88-95.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 88-95
-
-
Pogribna, M.1
Melnyk, S.2
Pogribny, I.3
Chango, A.4
Yi, P.5
-
15
-
-
40449109999
-
Systematic search for placental DNA-methylation markers on chromosome 21: toward a maternal plasma-based epigenetic test for fetal trisomy 21
-
Chim SS, Jin S, Lee TY, Lun FM, Lee WS, et al. (2008) Systematic search for placental DNA-methylation markers on chromosome 21: toward a maternal plasma-based epigenetic test for fetal trisomy 21. Clin Chem 54: 500-511.
-
(2008)
Clin Chem
, vol.54
, pp. 500-511
-
-
Chim, S.S.1
Jin, S.2
Lee, T.Y.3
Lun, F.M.4
Lee, W.S.5
-
16
-
-
65649095218
-
Sites of differential DNA methylation between placenta and peripheral blood: molecular markers for noninvasive prenatal diagnosis of aneuploidies
-
Papageorgiou EA, Fiegler H, Rakyan V, Beck S, Hulten M, et al. (2009) Sites of differential DNA methylation between placenta and peripheral blood: molecular markers for noninvasive prenatal diagnosis of aneuploidies. Am J Pathol 174: 1609-1618.
-
(2009)
Am J Pathol
, vol.174
, pp. 1609-1618
-
-
Papageorgiou, E.A.1
Fiegler, H.2
Rakyan, V.3
Beck, S.4
Hulten, M.5
-
17
-
-
70350440343
-
A microarray-based approach for the identification of epigenetic biomarkers for the noninvasive diagnosis of fetal disease
-
Chu T, Burke B, Bunce K, Surti U, Allen Hogge W, et al. (2009) A microarray-based approach for the identification of epigenetic biomarkers for the noninvasive diagnosis of fetal disease. Prenat Diagn 29: 1020-1030.
-
(2009)
Prenat Diagn
, vol.29
, pp. 1020-1030
-
-
Chu, T.1
Burke, B.2
Bunce, K.3
Surti, U.4
Allen Hogge, W.5
-
18
-
-
84862545652
-
DNA-Methylation Profiling of Fetal Tissues Reveals Marked Epigenetic Differences between Chorionic and Amniotic Samples
-
Eckmann-Scholz C, Bens S, Kolarova J, Schneppenheim S, Caliebe A, et al. (2012) DNA-Methylation Profiling of Fetal Tissues Reveals Marked Epigenetic Differences between Chorionic and Amniotic Samples. PLoS One 7: e39014.
-
(2012)
PLoS One
, vol.7
-
-
Eckmann-Scholz, C.1
Bens, S.2
Kolarova, J.3
Schneppenheim, S.4
Caliebe, A.5
-
19
-
-
84875404794
-
The UCSC Genome Browser database: extensions and updates 2013
-
Meyer LR, Zweig AS, Hinrichs AS, Karolchik D, Kuhn RM, et al. (2013) The UCSC Genome Browser database: extensions and updates 2013. Nucleic Acids Res 41: D64-69.
-
(2013)
Nucleic Acids Res
, vol.41
-
-
Meyer, L.R.1
Zweig, A.S.2
Hinrichs, A.S.3
Karolchik, D.4
Kuhn, R.M.5
-
20
-
-
63449103531
-
DNA methylation analysis of chromosome 21 gene promoters at single base pair and single allele resolution
-
Zhang Y, Rohde C, Tierling S, Jurkowski TP, Bock C, et al. (2009) DNA methylation analysis of chromosome 21 gene promoters at single base pair and single allele resolution. PLoS Genet 5: e1000438.
-
(2009)
PLoS Genet
, vol.5
-
-
Zhang, Y.1
Rohde, C.2
Tierling, S.3
Jurkowski, T.P.4
Bock, C.5
-
21
-
-
33751505540
-
DNA methylation profiling of human chromosomes 6, 20 and 22
-
Eckhardt F, Lewin J, Cortese R, Rakyan VK, Attwood J, et al. (2006) DNA methylation profiling of human chromosomes 6, 20 and 22. Nat Genet 38: 1378-1385.
-
(2006)
Nat Genet
, vol.38
, pp. 1378-1385
-
-
Eckhardt, F.1
Lewin, J.2
Cortese, R.3
Rakyan, V.K.4
Attwood, J.5
-
22
-
-
77649267695
-
Dynamic changes in the human methylome during differentiation
-
Laurent L, Wong E, Li G, Huynh T, Tsirigos A, et al. Dynamic changes in the human methylome during differentiation. Genome Res 20: 320-331.
-
Genome Res
, vol.20
, pp. 320-331
-
-
Laurent, L.1
Wong, E.2
Li, G.3
Huynh, T.4
Tsirigos, A.5
-
23
-
-
70450217879
-
Human DNA methylomes at base resolution show widespread epigenomic differences
-
Lister R, Pelizzola M, Dowen RH, Hawkins RD, Hon G, 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
Pelizzola, M.2
Dowen, R.H.3
Hawkins, R.D.4
Hon, G.5
-
24
-
-
84355163093
-
DNA-binding factors shape the mouse methylome at distal regulatory regions
-
Stadler MB, Murr R, Burger L, Ivanek R, Lienert F, et al. (2011) DNA-binding factors shape the mouse methylome at distal regulatory regions. Nature 480: 490-495.
-
(2011)
Nature
, vol.480
, pp. 490-495
-
-
Stadler, M.B.1
Murr, R.2
Burger, L.3
Ivanek, R.4
Lienert, F.5
-
25
-
-
49649125042
-
Genome-scale DNA methylation maps of pluripotent and differentiated cells
-
Meissner A, Mikkelsen TS, Gu H, Wernig M, Hanna J, et al. (2008) Genome-scale DNA methylation maps of pluripotent and differentiated cells. Nature 454: 766-770.
-
(2008)
Nature
, vol.454
, pp. 766-770
-
-
Meissner, A.1
Mikkelsen, T.S.2
Gu, H.3
Wernig, M.4
Hanna, J.5
-
26
-
-
83755224300
-
Significance analysis and statistical dissection of variably methylated regions
-
Jaffe AE, Feinberg AP, Irizarry RA, Leek JT, (2012) Significance analysis and statistical dissection of variably methylated regions. Biostatistics 13: 166-178.
-
(2012)
Biostatistics
, vol.13
, pp. 166-178
-
-
Jaffe, A.E.1
Feinberg, A.P.2
Irizarry, R.A.3
Leek, J.T.4
-
27
-
-
78649715229
-
Altered DNA methylation in leukocytes with trisomy 21
-
Kerkel K, Schupf N, Hatta K, Pang D, Salas M, et al. Altered DNA methylation in leukocytes with trisomy 21. PLoS Genet 6: e1001212.
-
PLoS Genet
, vol.6
-
-
Kerkel, K.1
Schupf, N.2
Hatta, K.3
Pang, D.4
Salas, M.5
-
28
-
-
66149146320
-
Conversion of 5-methylcytosine to 5-hydroxymethylcytosine in mammalian DNA by MLL partner TET1
-
Tahiliani M, Koh KP, Shen Y, Pastor WA, Bandukwala H, et al. (2009) Conversion of 5-methylcytosine to 5-hydroxymethylcytosine in mammalian DNA by MLL partner TET1. Science 324: 930-935.
-
(2009)
Science
, vol.324
, pp. 930-935
-
-
Tahiliani, M.1
Koh, K.P.2
Shen, Y.3
Pastor, W.A.4
Bandukwala, H.5
-
29
-
-
80052495940
-
Tet-mediated formation of 5-carboxylcytosine and its excision by TDG in mammalian DNA
-
He YF, Li BZ, Li Z, Liu P, Wang Y, et al. (2011) Tet-mediated formation of 5-carboxylcytosine and its excision by TDG in mammalian DNA. Science 333: 1303-1307.
-
(2011)
Science
, vol.333
, pp. 1303-1307
-
-
He, Y.F.1
Li, B.Z.2
Li, Z.3
Liu, P.4
Wang, Y.5
-
30
-
-
80052461558
-
Tet proteins can convert 5-methylcytosine to 5-formylcytosine and 5-carboxylcytosine
-
Ito S, Shen L, Dai Q, Wu SC, Collins LB, et al. (2011) Tet proteins can convert 5-methylcytosine to 5-formylcytosine and 5-carboxylcytosine. Science 333: 1300-1303.
-
(2011)
Science
, vol.333
, pp. 1300-1303
-
-
Ito, S.1
Shen, L.2
Dai, Q.3
Wu, S.C.4
Collins, L.B.5
-
31
-
-
79956323623
-
Dynamic regulation of 5-hydroxymethylcytosine in mouse ES cells and during differentiation
-
Ficz G, Branco MR, Seisenberger S, Santos F, Krueger F, et al. (2011) Dynamic regulation of 5-hydroxymethylcytosine in mouse ES cells and during differentiation. Nature 473: 398-402.
-
(2011)
Nature
, vol.473
, pp. 398-402
-
-
Ficz, G.1
Branco, M.R.2
Seisenberger, S.3
Santos, F.4
Krueger, F.5
-
32
-
-
79961139741
-
Tet1 is dispensable for maintaining pluripotency and its loss is compatible with embryonic and postnatal development
-
Dawlaty MM, Ganz K, Powell BE, Hu YC, Markoulaki S, et al. (2011) Tet1 is dispensable for maintaining pluripotency and its loss is compatible with embryonic and postnatal development. Cell Stem Cell 9: 166-175.
-
(2011)
Cell Stem Cell
, vol.9
, pp. 166-175
-
-
Dawlaty, M.M.1
Ganz, K.2
Powell, B.E.3
Hu, Y.C.4
Markoulaki, S.5
-
33
-
-
77955411499
-
Gene network disruptions and neurogenesis defects in the adult Ts1Cje mouse model of Down syndrome
-
Hewitt CA, Ling KH, Merson TD, Simpson KM, Ritchie ME, et al. (2010) Gene network disruptions and neurogenesis defects in the adult Ts1Cje mouse model of Down syndrome. PLoS One 5: e11561.
-
(2010)
PLoS One
, vol.5
-
-
Hewitt, C.A.1
Ling, K.H.2
Merson, T.D.3
Simpson, K.M.4
Ritchie, M.E.5
-
34
-
-
41149164894
-
Neurogenesis impairment and increased cell death reduce total neuron number in the hippocampal region of fetuses with Down syndrome
-
Guidi S, Bonasoni P, Ceccarelli C, Santini D, Gualtieri F, et al. (2008) Neurogenesis impairment and increased cell death reduce total neuron number in the hippocampal region of fetuses with Down syndrome. Brain Pathol 18: 180-197.
-
(2008)
Brain Pathol
, vol.18
, pp. 180-197
-
-
Guidi, S.1
Bonasoni, P.2
Ceccarelli, C.3
Santini, D.4
Gualtieri, F.5
-
35
-
-
34548102066
-
Cell cycle alteration and decreased cell proliferation in the hippocampal dentate gyrus and in the neocortical germinal matrix of fetuses with Down syndrome and in Ts65Dn mice
-
Contestabile A, Fila T, Ceccarelli C, Bonasoni P, Bonapace L, et al. (2007) Cell cycle alteration and decreased cell proliferation in the hippocampal dentate gyrus and in the neocortical germinal matrix of fetuses with Down syndrome and in Ts65Dn mice. Hippocampus 17: 665-678.
-
(2007)
Hippocampus
, vol.17
, pp. 665-678
-
-
Contestabile, A.1
Fila, T.2
Ceccarelli, C.3
Bonasoni, P.4
Bonapace, L.5
-
36
-
-
77955037842
-
Olig1 and Olig2 triplication causes developmental brain defects in Down syndrome
-
Chakrabarti L, Best TK, Cramer NP, Carney RS, Isaac JT, et al. (2010) Olig1 and Olig2 triplication causes developmental brain defects in Down syndrome. Nat Neurosci 13: 927-934.
-
(2010)
Nat Neurosci
, vol.13
, pp. 927-934
-
-
Chakrabarti, L.1
Best, T.K.2
Cramer, N.P.3
Carney, R.S.4
Isaac, J.T.5
-
37
-
-
64549130400
-
DYRK1A interacts with the REST/NRSF-SWI/SNF chromatin remodelling complex to deregulate gene clusters involved in the neuronal phenotypic traits of Down syndrome
-
Lepagnol-Bestel AM, Zvara A, Maussion G, Quignon F, Ngimbous B, et al. (2009) DYRK1A interacts with the REST/NRSF-SWI/SNF chromatin remodelling complex to deregulate gene clusters involved in the neuronal phenotypic traits of Down syndrome. Hum Mol Genet 18: 1405-1414.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 1405-1414
-
-
Lepagnol-Bestel, A.M.1
Zvara, A.2
Maussion, G.3
Quignon, F.4
Ngimbous, B.5
-
38
-
-
84861990517
-
Base-resolution analysis of 5-hydroxymethylcytosine in the Mammalian genome
-
Yu M, Hon GC, Szulwach KE, Song CX, Zhang L, et al. (2012) Base-resolution analysis of 5-hydroxymethylcytosine in the Mammalian genome. Cell 149: 1368-1380.
-
(2012)
Cell
, vol.149
, pp. 1368-1380
-
-
Yu, M.1
Hon, G.C.2
Szulwach, K.E.3
Song, C.X.4
Zhang, L.5
-
39
-
-
71249116003
-
Mannan-binding lectin deficiency increases the risk of recurrent infections in children with Down's syndrome
-
Nisihara RM, Utiyama SR, Oliveira NP, Messias-Reason IJ, (2010) Mannan-binding lectin deficiency increases the risk of recurrent infections in children with Down's syndrome. Hum Immunol 71: 63-66.
-
(2010)
Hum Immunol
, vol.71
, pp. 63-66
-
-
Nisihara, R.M.1
Utiyama, S.R.2
Oliveira, N.P.3
Messias-Reason, I.J.4
-
40
-
-
79951930596
-
REST: transcriptional and epigenetic regulator
-
Bithell A, (2011) REST: transcriptional and epigenetic regulator. Epigenomics 3: 47-58.
-
(2011)
Epigenomics
, vol.3
, pp. 47-58
-
-
Bithell, A.1
-
41
-
-
0037176537
-
Neuronal target genes of the neuron-restrictive silencer factor in neurospheres derived from fetuses with Down's syndrome: a gene expression study
-
Bahn S, Mimmack M, Ryan M, Caldwell MA, Jauniaux E, et al. (2002) Neuronal target genes of the neuron-restrictive silencer factor in neurospheres derived from fetuses with Down's syndrome: a gene expression study. Lancet 359: 310-315.
-
(2002)
Lancet
, vol.359
, pp. 310-315
-
-
Bahn, S.1
Mimmack, M.2
Ryan, M.3
Caldwell, M.A.4
Jauniaux, E.5
-
42
-
-
51149115754
-
DYRK1A-dosage imbalance perturbs NRSF/REST levels, deregulating pluripotency and embryonic stem cell fate in Down syndrome
-
Canzonetta C, Mulligan C, Deutsch S, Ruf S, O'Doherty A, et al. (2008) DYRK1A-dosage imbalance perturbs NRSF/REST levels, deregulating pluripotency and embryonic stem cell fate in Down syndrome. Am J Hum Genet 83: 388-400.
-
(2008)
Am J Hum Genet
, vol.83
, pp. 388-400
-
-
Canzonetta, C.1
Mulligan, C.2
Deutsch, S.3
Ruf, S.4
O'Doherty, A.5
-
43
-
-
80054994297
-
Evidence for widespread changes in promoter methylation profile in human placenta in response to increasing gestational age and environmental/stochastic factors
-
Novakovic B, Yuen RK, Gordon L, Penaherrera MS, Sharkey A, et al. (2011) Evidence for widespread changes in promoter methylation profile in human placenta in response to increasing gestational age and environmental/stochastic factors. BMC Genomics 12: 529.
-
(2011)
BMC Genomics
, vol.12
, pp. 529
-
-
Novakovic, B.1
Yuen, R.K.2
Gordon, L.3
Penaherrera, M.S.4
Sharkey, A.5
-
44
-
-
67749148222
-
The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies
-
Korbel JO, Tirosh-Wagner T, Urban AE, Chen XN, Kasowski M, et al. (2009) The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies. Proc Natl Acad Sci U S A 106: 12031-12036.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 12031-12036
-
-
Korbel, J.O.1
Tirosh-Wagner, T.2
Urban, A.E.3
Chen, X.N.4
Kasowski, M.5
-
45
-
-
62849113692
-
Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21
-
Lyle R, Bena F, Gagos S, Gehrig C, Lopez G, et al. (2009) Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21. Eur J Hum Genet 17: 454-466.
-
(2009)
Eur J Hum Genet
, vol.17
, pp. 454-466
-
-
Lyle, R.1
Bena, F.2
Gagos, S.3
Gehrig, C.4
Lopez, G.5
-
46
-
-
83055172862
-
On the promise of pharmacotherapies targeted at cognitive and neurodegenerative components of Down syndrome
-
Costa AC, (2011) On the promise of pharmacotherapies targeted at cognitive and neurodegenerative components of Down syndrome. Dev Neurosci 33: 414-427.
-
(2011)
Dev Neurosci
, vol.33
, pp. 414-427
-
-
Costa, A.C.1
-
47
-
-
80051768234
-
Is it possible to improve neurodevelopmental abnormalities in Down syndrome?
-
Bartesaghi R, Guidi S, Ciani E, (2011) Is it possible to improve neurodevelopmental abnormalities in Down syndrome? Rev Neurosci 22: 419-455.
-
(2011)
Rev Neurosci
, vol.22
, pp. 419-455
-
-
Bartesaghi, R.1
Guidi, S.2
Ciani, E.3
-
48
-
-
62349130698
-
Ultrafast and memory-efficient alignment of short DNA sequences to the human genome
-
Langmead B, Trapnell C, Pop M, Salzberg SL, (2009) Ultrafast and memory-efficient 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.L.4
|