-
1
-
-
84908875580
-
A new workflow for whole-genome sequencing of single human cells
-
Binder V., Bartenhagen C., Okpanyi V., Gombert M., Moehlendick B., Behrens B., Klein H.U., Rieder H., Ida Krell P.F., Dugas M., Stoecklein N.H., Borkhardt A. A new workflow for whole-genome sequencing of single human cells. Hum. Mutat. 2014, 35:1260-1270.
-
(2014)
Hum. Mutat.
, vol.35
, pp. 1260-1270
-
-
Binder, V.1
Bartenhagen, C.2
Okpanyi, V.3
Gombert, M.4
Moehlendick, B.5
Behrens, B.6
Klein, H.U.7
Rieder, H.8
Ida Krell, P.F.9
Dugas, M.10
Stoecklein, N.H.11
Borkhardt, A.12
-
2
-
-
84879791544
-
Whole genome amplification and its application in forensic individual identification
-
Cai H.Q., Liu H.T., Shi B., Li A., Tang W.R., Luo Y. Whole genome amplification and its application in forensic individual identification. Yi Chuan 2010, 32:1119-1125.
-
(2010)
Yi Chuan
, vol.32
, pp. 1119-1125
-
-
Cai, H.Q.1
Liu, H.T.2
Shi, B.3
Li, A.4
Tang, W.R.5
Luo, Y.6
-
3
-
-
84903289930
-
Reliable single cell array CGH for clinical samples
-
Czyz Z.T., Hoffmann M., Schlimok G., Polzer B., Klein C.A. Reliable single cell array CGH for clinical samples. PLoS One 2014, 9:e85907.
-
(2014)
PLoS One
, vol.9
, pp. e85907
-
-
Czyz, Z.T.1
Hoffmann, M.2
Schlimok, G.3
Polzer, B.4
Klein, C.A.5
-
4
-
-
84920645442
-
A quantitative comparison of single-cell whole genome amplification methods
-
de Bourcy C.F., De Vlaminck I., Kanbar J.N., Wang J., Gawad C., Quake S.R. A quantitative comparison of single-cell whole genome amplification methods. PLoS One 2014, 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
-
5
-
-
18344396798
-
Comprehensive human genome amplification using multiple displacement amplification
-
Dean F.B., Hosono S., Fang L., Wu X., Faruqi A.F., Bray-Ward P., Sun Z., Zong Q., Du Y., Du J., Driscoll M., Song W., Kingsmore S.F., Egholm M., Lasken R.S. Comprehensive human genome amplification using multiple displacement amplification. Proc. Natl. Acad. Sci. USA 2002, 99:5261-5266.
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 5261-5266
-
-
Dean, F.B.1
Hosono, S.2
Fang, L.3
Wu, X.4
Faruqi, A.F.5
Bray-Ward, P.6
Sun, Z.7
Zong, Q.8
Du, Y.9
Du, J.10
Driscoll, M.11
Song, W.12
Kingsmore, S.F.13
Egholm, M.14
Lasken, R.S.15
-
6
-
-
0029038302
-
Allelic drop-out and preferential amplification in single cells and human blastomeres: implications for preimplantation diagnosis of sex and cystic fibrosis
-
Findlay I., Ray P., Quirke P., Rutherford A., Lilford R. Allelic drop-out and preferential amplification in single cells and human blastomeres: implications for preimplantation diagnosis of sex and cystic fibrosis. Hum. Reprod. 1995, 10:1609-1618.
-
(1995)
Hum. Reprod.
, vol.10
, pp. 1609-1618
-
-
Findlay, I.1
Ray, P.2
Quirke, P.3
Rutherford, A.4
Lilford, R.5
-
7
-
-
84899932270
-
Development and validation of a next-generation sequencing-based protocol for 24-chromosome aneuploidy screening of embryos
-
Fiorentino F., Biricik A., Bono S., Spizzichino L., Cotroneo E., Cottone G., Kokocinski F., Michel C.E. Development and validation of a next-generation sequencing-based protocol for 24-chromosome aneuploidy screening of embryos. Fertil. Steril. 2014, 101:1375-1382.
-
(2014)
Fertil. Steril.
, vol.101
, pp. 1375-1382
-
-
Fiorentino, F.1
Biricik, A.2
Bono, S.3
Spizzichino, L.4
Cotroneo, E.5
Cottone, G.6
Kokocinski, F.7
Michel, C.E.8
-
8
-
-
79959426439
-
PGD for reciprocal and Robertsonian translocations using array comparative genomic hybridization
-
Fiorentino F., Spizzichino L., Bono S., Biricik A., Kokkali G., Rienzi L., Ubaldi F.M., Iammarrone E., Gordon A., Pantos K. PGD for reciprocal and Robertsonian translocations using array comparative genomic hybridization. Hum. Reprod. 2011, 26:1925-1935.
-
(2011)
Hum. Reprod.
, vol.26
, pp. 1925-1935
-
-
Fiorentino, F.1
Spizzichino, L.2
Bono, S.3
Biricik, A.4
Kokkali, G.5
Rienzi, L.6
Ubaldi, F.M.7
Iammarrone, E.8
Gordon, A.9
Pantos, K.10
-
9
-
-
38949113780
-
Nucleic acid isothermal amplification technologies: a review
-
Gill P., Ghaemi A. Nucleic acid isothermal amplification technologies: a review. Nucleosides Nucleotides Nucleic Acids 2008, 27:224-243.
-
(2008)
Nucleosides Nucleotides Nucleic Acids
, vol.27
, pp. 224-243
-
-
Gill, P.1
Ghaemi, A.2
-
10
-
-
84883364133
-
24-chromosome copy number analysis: a comparison of available technologies
-
Handyside A.H. 24-chromosome copy number analysis: a comparison of available technologies. Fertil. Steril. 2013, 100:595-602.
-
(2013)
Fertil. Steril.
, vol.100
, pp. 595-602
-
-
Handyside, A.H.1
-
11
-
-
84893594630
-
Genome analyses of single human oocytes
-
Hou Y., Fan W., Yan L., Li R., Lian Y., Huang J., Li J., Xu L., Tang F., Xie X.S., Qiao J. Genome analyses of single human oocytes. Cell 2013, 155:1492-1506.
-
(2013)
Cell
, vol.155
, pp. 1492-1506
-
-
Hou, Y.1
Fan, W.2
Yan, L.3
Li, R.4
Lian, Y.5
Huang, J.6
Li, J.7
Xu, L.8
Tang, F.9
Xie, X.S.10
Qiao, J.11
-
12
-
-
77949587649
-
Fast and accurate long-read alignment with Burrows-Wheeler transform
-
Li H., Durbin R. Fast and accurate long-read alignment with Burrows-Wheeler transform. Bioinformatics 2010, 26:589-595.
-
(2010)
Bioinformatics
, vol.26
, pp. 589-595
-
-
Li, H.1
Durbin, R.2
-
13
-
-
84921971016
-
Validation of multiple annealing and looping-based amplification cycle sequencing for 24-chromosome aneuploidy screening of cleavage-stage embryos
-
Huang J., Yan L., Fan W., Zhao N., Zhang Y., Tang F., Xie X.S., Qiao J. Validation of multiple annealing and looping-based amplification cycle sequencing for 24-chromosome aneuploidy screening of cleavage-stage embryos. Fertil. Steril. 2014, 102:1685-1691.
-
(2014)
Fertil. Steril.
, vol.102
, pp. 1685-1691
-
-
Huang, J.1
Yan, L.2
Fan, W.3
Zhao, N.4
Zhang, Y.5
Tang, F.6
Xie, X.S.7
Qiao, J.8
-
14
-
-
84877601474
-
Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing
-
Liang D., Lv W., Wang H., Xu L., Liu J., Li H., Hu L., Peng Y., Wu L. Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing. Prenat. Diagn. 2013, 33:409-415.
-
(2013)
Prenat. Diagn.
, vol.33
, pp. 409-415
-
-
Liang, D.1
Lv, W.2
Wang, H.3
Xu, L.4
Liu, J.5
Li, H.6
Hu, L.7
Peng, Y.8
Wu, L.9
-
15
-
-
84906281405
-
Copy number variation sequencing for comprehensive diagnosis of chromosome disease syndromes
-
Liang D., Peng Y., Lv W., Deng L., Zhang Y., Li H., Yang P., Zhang J., Song Z., Xu G., Cram D.S., Wu L. Copy number variation sequencing for comprehensive diagnosis of chromosome disease syndromes. J. Mol. Diagn. 2014, 16:519-526.
-
(2014)
J. Mol. Diagn.
, vol.16
, pp. 519-526
-
-
Liang, D.1
Peng, Y.2
Lv, W.3
Deng, L.4
Zhang, Y.5
Li, H.6
Yang, P.7
Zhang, J.8
Song, Z.9
Xu, G.10
Cram, D.S.11
Wu, L.12
-
16
-
-
84866694368
-
Preimplantation genetic diagnosis for aneuploidy and translocations using array comparative genomic hybridization
-
Munne S. Preimplantation genetic diagnosis for aneuploidy and translocations using array comparative genomic hybridization. Curr. Genomics 2012, 13:463-470.
-
(2012)
Curr. Genomics
, vol.13
, pp. 463-470
-
-
Munne, S.1
-
17
-
-
84881133553
-
Successful PGD for late infantile neuronal ceroid lipofuscinosis achieved by combined chromosome and TPP1 gene analysis
-
Shen J., Cram D.S., Wu W., Cai L., Yang X., Sun X., Cui Y., Liu J. Successful PGD for late infantile neuronal ceroid lipofuscinosis achieved by combined chromosome and TPP1 gene analysis. Reprod. Biomed. Online 2013, 27:176-183.
-
(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
Sun, X.6
Cui, Y.7
Liu, J.8
-
18
-
-
0026736251
-
Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer
-
Telenius H., Carter N.P., Bebb C.E., Nordenskjold M., Ponder B.A., Tunnacliffe A. Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer. Genomics 1992, 13:718-725.
-
(1992)
Genomics
, vol.13
, pp. 718-725
-
-
Telenius, H.1
Carter, N.P.2
Bebb, C.E.3
Nordenskjold, M.4
Ponder, B.A.5
Tunnacliffe, A.6
-
19
-
-
37249032736
-
Spatial smoothing and hot spot detection for CGH data using fused lasso
-
Tibshirani R., Wang P. Spatial smoothing and hot spot detection for CGH data using fused lasso. Biostatistics 2008, 9:18-29.
-
(2008)
Biostatistics
, vol.9
, pp. 18-29
-
-
Tibshirani, R.1
Wang, P.2
-
20
-
-
79957532985
-
Single-cell whole-genome amplification technique impacts the accuracy of SNP microarray-based genotyping and copy number analyses
-
Treff N.R., Su J., Tao X., Northrop L.E., Scott R.T. Single-cell whole-genome amplification technique impacts the accuracy of SNP microarray-based genotyping and copy number analyses. Mol. Hum. Reprod. 2011, 17:335-343.
-
(2011)
Mol. Hum. Reprod.
, vol.17
, pp. 335-343
-
-
Treff, N.R.1
Su, J.2
Tao, X.3
Northrop, L.E.4
Scott, R.T.5
-
21
-
-
66749169417
-
Chromosome instability is common in human cleavage-stage embryos
-
Vanneste E., Voet T., Le Caignec C., Ampe M., Konings P., Melotte C., Debrock S., Amyere M., Vikkula M., Schuit F., Fryns J.P., Verbeke G., D'Hooghe T., Moreau Y., Vermeesch J.R. Chromosome instability is common in human cleavage-stage embryos. Nat. Med. 2009, 15:577-583.
-
(2009)
Nat. Med.
, vol.15
, pp. 577-583
-
-
Vanneste, E.1
Voet, T.2
Le Caignec, C.3
Ampe, M.4
Konings, P.5
Melotte, C.6
Debrock, S.7
Amyere, M.8
Vikkula, M.9
Schuit, F.10
Fryns, J.P.11
Verbeke, G.12
D'Hooghe, T.13
Moreau, Y.14
Vermeesch, J.R.15
-
22
-
-
79959689944
-
Breakage-fusion-bridge cycles leading to inv dup del occur in human cleavage stage embryos
-
Voet T., Vanneste E., Van der Aa N., Melotte C., Jackmaert S., Vandendael T., Declercq M., Debrock S., Fryns J.P., Moreau Y., D'Hooghe T., Vermeesch J.R. Breakage-fusion-bridge cycles leading to inv dup del occur in human cleavage stage embryos. Hum. Mutat. 2011, 32:783-793.
-
(2011)
Hum. Mutat.
, vol.32
, pp. 783-793
-
-
Voet, T.1
Vanneste, E.2
Van der Aa, N.3
Melotte, C.4
Jackmaert, S.5
Vandendael, T.6
Declercq, M.7
Debrock, S.8
Fryns, J.P.9
Moreau, Y.10
D'Hooghe, T.11
Vermeesch, J.R.12
-
23
-
-
84906790977
-
A PGD pregnancy achieved by embryo copy number variation sequencing with confirmation by non-invasive prenatal diagnosis
-
Wang H., Wang L., Ma M., Song Z., Zhang J., Xu G., Fan J., Li N., Cram D.S., Yao Y. A PGD pregnancy achieved by embryo copy number variation sequencing with confirmation by non-invasive prenatal diagnosis. J. Genet. Genomics 2014, 41:453-456.
-
(2014)
J. Genet. Genomics
, vol.41
, pp. 453-456
-
-
Wang, H.1
Wang, L.2
Ma, M.3
Song, Z.4
Zhang, J.5
Xu, G.6
Fan, J.7
Li, N.8
Cram, D.S.9
Yao, Y.10
-
24
-
-
84928823213
-
Validation of copy number variation sequencing for detecting chromosome imbalances in human preimplantation embryos
-
Wang L., Cram D.S., Shen J., Wang X., Zhang J., Song Z., Xu G., Li N., Fan J., Wang S., Luo Y., Wang J., Yu L., Liu J., Yao Y. Validation of copy number variation sequencing for detecting chromosome imbalances in human preimplantation embryos. Biol. Reprod. 2014, 91:37.
-
(2014)
Biol. Reprod.
, vol.91
, pp. 37
-
-
Wang, L.1
Cram, D.S.2
Shen, J.3
Wang, X.4
Zhang, J.5
Song, Z.6
Xu, G.7
Li, N.8
Fan, J.9
Wang, S.10
Luo, Y.11
Wang, J.12
Yu, L.13
Liu, J.14
Yao, Y.15
-
25
-
-
84903794560
-
Detection of chromosomal aneuploidy in human preimplantation embryos by next-generation sequencing
-
Wang L., Wang X., Zhang J., Song Z., Wang S., Gao Y., Wang J., Luo Y., Niu Z., Yue X., Xu G., Cram D.S., Yao Y. Detection of chromosomal aneuploidy in human preimplantation embryos by next-generation sequencing. Biol. Reprod. 2014, 90:95.
-
(2014)
Biol. Reprod.
, vol.90
, pp. 95
-
-
Wang, L.1
Wang, X.2
Zhang, J.3
Song, Z.4
Wang, S.5
Gao, Y.6
Wang, J.7
Luo, Y.8
Niu, Z.9
Yue, X.10
Xu, G.11
Cram, D.S.12
Yao, Y.13
-
26
-
-
84891822473
-
Maternal mosaicism is a significant contributor to discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing
-
Wang Y., Chen Y., Tian F., Zhang J., Song Z., Wu Y., Han X., Hu W., Ma D., Cram D., Cheng W. Maternal mosaicism is a significant contributor to discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing. Clin. Chem. 2014, 60:251-259.
-
(2014)
Clin. Chem.
, vol.60
, pp. 251-259
-
-
Wang, Y.1
Chen, Y.2
Tian, F.3
Zhang, J.4
Song, Z.5
Wu, Y.6
Han, X.7
Hu, W.8
Ma, D.9
Cram, D.10
Cheng, W.11
-
27
-
-
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 J.C., Fragouli E., Munne S. 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. 2014, 51:553-562.
-
(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
Fragouli, E.6
Munne, S.7
-
28
-
-
84876951707
-
Massively parallel sequencing for chromosomal abnormality testing in trophectoderm cells of human blastocysts
-
Yin X., Tan K., Vajta G., Jiang H., Tan Y., Zhang C., Chen F., Chen S., Pan X., Gong C., Li X., Lin C., Gao Y., Liang Y., Yi X., Mu F., Zhao L., Peng H., Xiong B., Zhang S., Cheng D., Lu G., Zhang X., Lin G., Wang W. Massively parallel sequencing for chromosomal abnormality testing in trophectoderm cells of human blastocysts. Biol. Reprod. 2013, 88:69.
-
(2013)
Biol. Reprod.
, vol.88
, pp. 69
-
-
Yin, X.1
Tan, K.2
Vajta, G.3
Jiang, H.4
Tan, Y.5
Zhang, C.6
Chen, F.7
Chen, S.8
Pan, X.9
Gong, C.10
Li, X.11
Lin, C.12
Gao, Y.13
Liang, Y.14
Yi, X.15
Mu, F.16
Zhao, L.17
Peng, H.18
Xiong, B.19
Zhang, S.20
Cheng, D.21
Lu, G.22
Zhang, X.23
Lin, G.24
Wang, W.25
more..
-
29
-
-
84907889523
-
Microfluidic whole genome amplification device for single cell sequencing
-
Yu Z., Lu S., Huang Y. Microfluidic whole genome amplification device for single cell sequencing. Anal. Chem. 2014, 86:9386-9390.
-
(2014)
Anal. Chem.
, vol.86
, pp. 9386-9390
-
-
Yu, Z.1
Lu, S.2
Huang, Y.3
-
30
-
-
0026755807
-
Whole genome amplification from a single cell: implications for genetic analysis
-
Zhang L., Cui X., Schmitt K., Hubert R., Navidi W., Arnheim N. Whole genome amplification from a single cell: implications for genetic analysis. Proc. Natl. Acad. Sci. USA 1992, 89:5847-5851.
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 5847-5851
-
-
Zhang, L.1
Cui, X.2
Schmitt, K.3
Hubert, R.4
Navidi, W.5
Arnheim, N.6
-
31
-
-
79251567377
-
Whole genome amplification in preimplantation genetic diagnosis
-
Zheng Y.M., Wang N., Li L., Jin F. Whole genome amplification in preimplantation genetic diagnosis. J. Zhejiang Univ. Sci. B 2011, 12:1-11.
-
(2011)
J. Zhejiang Univ. Sci. B
, vol.12
, pp. 1-11
-
-
Zheng, Y.M.1
Wang, N.2
Li, L.3
Jin, F.4
-
32
-
-
84871461434
-
Genome-wide detection of single-nucleotide and copy-number variations of a single human cell
-
Zong C., Lu S., Chapman A.R., Xie X.S. Genome-wide detection of single-nucleotide and copy-number variations of a single human cell. Science 2012, 338:1622-1626.
-
(2012)
Science
, vol.338
, pp. 1622-1626
-
-
Zong, C.1
Lu, S.2
Chapman, A.R.3
Xie, X.S.4
|