-
1
-
-
84896769549
-
Clinical Interpretation and Implications of Whole-Genome Sequencing
-
Dewey FE, Grove ME, Pan CP, Goldstein BA, Bernstein JA, Chaib H, et al. Clinical Interpretation and Implications of Whole-Genome Sequencing. JAMA. 2014;311:1035-44.
-
(2014)
JAMA.
, vol.311
, pp. 1035-1044
-
-
Dewey, F.E.1
Grove, M.E.2
Pan, C.P.3
Goldstein, B.A.4
Bernstein, J.A.5
Chaib, H.6
-
2
-
-
84946606845
-
Sequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence Data
-
Dewey FE, Grove ME, Priest JR, Waggott D, Batra P, Miller CL, et al. Sequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence Data. PLoS Genet. Public Library of Science. 2015;11(10):e1005496.
-
(2015)
PLoS Genet. Public Library of Science
, vol.11
, Issue.10
-
-
Dewey, F.E.1
Grove, M.E.2
Priest, J.R.3
Waggott, D.4
Batra, P.5
Miller, C.L.6
-
4
-
-
84921850275
-
Reducing INDEL calling errors in whole genome and exome sequencing data
-
Fang H, Wu YY, Narzisi G, O'Rawe JA, Barron LTJ, Rosenbaum J, et al. Reducing INDEL calling errors in whole genome and exome sequencing data. Genome Med. 2014;6:17.
-
(2014)
Genome Med.
, vol.6
, pp. 17
-
-
Fang, H.1
Wu, Y.Y.2
Narzisi, G.3
O'Rawe, J.A.4
Barron, L.T.J.5
Rosenbaum, J.6
-
5
-
-
84875312984
-
Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing
-
O'Rawe J, Jiang T, Sun GQ, Wu YY, Wang W, Hu JC, et al. Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing. Genome Med. 2013;5:18.
-
(2013)
Genome Med.
, vol.5
, pp. 18
-
-
O'Rawe, J.1
Jiang, T.2
Sun, G.Q.3
Wu, Y.Y.4
Wang, W.5
Hu, J.C.6
-
6
-
-
84929455376
-
Estimating genotype error rates from high-coverage next-generation sequence data
-
Wall JD, Tang LF, Zerbe B, Kvale MN, Kwok PY, Schaefer C, et al. Estimating genotype error rates from high-coverage next-generation sequence data. Genome Res. 2014;24:1734-9.
-
(2014)
Genome Res.
, vol.24
, pp. 1734-1739
-
-
Wall, J.D.1
Tang, L.F.2
Zerbe, B.3
Kvale, M.N.4
Kwok, P.Y.5
Schaefer, C.6
-
7
-
-
84936765000
-
New insights into the performance of human whole-exome capture platforms
-
Meienberg J, Zerjavic K, Keller I, Okoniewski M, Patrignani A, Ludin K, et al. New insights into the performance of human whole-exome capture platforms. Nucleic Acids Res. 2015;43:e76.
-
(2015)
Nucleic Acids Res.
, vol.43
, pp. e76
-
-
Meienberg, J.1
Zerjavic, K.2
Keller, I.3
Okoniewski, M.4
Patrignani, A.5
Ludin, K.6
-
8
-
-
84857990816
-
A comparative analysis of exome capture
-
Parla JS, Iossifov I, Grabill I, Spector MS, Kramer M, McCombie WR. A comparative analysis of exome capture. Genome Biol. 2011;12:R97.
-
(2011)
Genome Biol.
, vol.12
, pp. R97
-
-
Parla, J.S.1
Iossifov, I.2
Grabill, I.3
Spector, M.S.4
Kramer, M.5
McCombie, W.R.6
-
9
-
-
80054757012
-
Performance comparison of exome DNA sequencing technologies
-
Clark MJ, Chen R, Lam HYK, Karczewski KJ, Euskirchen G, Butte AJ, et al. Performance comparison of exome DNA sequencing technologies. Nat Biotechnol. 2011;29:908-14.
-
(2011)
Nat Biotechnol.
, vol.29
, pp. 908-914
-
-
Clark, M.J.1
Chen, R.2
Lam, H.Y.K.3
Karczewski, K.J.4
Euskirchen, G.5
Butte, A.J.6
-
10
-
-
84855281420
-
Repetitive elements may comprise over two-thirds of the human genome
-
de Koning AP, Gu W, Castoe TA, Batzer MA, Pollock DD. Repetitive elements may comprise over two-thirds of the human genome. PLoS Genet. 2011;7:e1002384.
-
(2011)
PLoS Genet.
, vol.7
, pp. e1002384
-
-
Koning, A.P.1
Gu, W.2
Castoe, T.A.3
Batzer, M.A.4
Pollock, D.D.5
-
11
-
-
37648999313
-
Distinguishing protein-coding and noncoding genes in the human genome
-
Clamp M, Fry B, Kamal M, Xie X, Cuff J, Lin MF, et al. Distinguishing protein-coding and noncoding genes in the human genome. Proc Natl Acad Sci U S A. 2007;104:19428-33.
-
(2007)
Proc Natl Acad Sci U S A.
, vol.104
, pp. 19428-19433
-
-
Clamp, M.1
Fry, B.2
Kamal, M.3
Xie, X.4
Cuff, J.5
Lin, M.F.6
-
12
-
-
84901059842
-
Biophysics, pathophysiology, and pharmacology of ion channel gating pores
-
Moreau A, Gosselin-Badaroudine P, Chahine M. Biophysics, pathophysiology, and pharmacology of ion channel gating pores. Front Pharmacol. 2014;5:53.
-
(2014)
Front Pharmacol.
, vol.5
, pp. 53
-
-
Moreau, A.1
Gosselin-Badaroudine, P.2
Chahine, M.3
-
13
-
-
84863116742
-
A systematic survey of loss-of-function variants in human protein-coding genes
-
MacArthur DG, Balasubramanian S, Frankish A, Huang N, Morris J, Walter K, et al. A systematic survey of loss-of-function variants in human protein-coding genes. Science. 2012;335:823-8.
-
(2012)
Science.
, vol.335
, pp. 823-828
-
-
MacArthur, D.G.1
Balasubramanian, S.2
Frankish, A.3
Huang, N.4
Morris, J.5
Walter, K.6
-
14
-
-
73149123343
-
Genetic diagnosis by whole exome capture and massively parallel DNA sequencing
-
Choi M, Scholl UI, Ji W, Liu T, Tikhonova IR, Zumbo P, et al. Genetic diagnosis by whole exome capture and massively parallel DNA sequencing. Proc Natl Acad Sci U S A. 2009;106:19096-101.
-
(2009)
Proc Natl Acad Sci U S A.
, vol.106
, pp. 19096-19101
-
-
Choi, M.1
Scholl, U.I.2
Ji, W.3
Liu, T.4
Tikhonova, I.R.5
Zumbo, P.6
-
16
-
-
55549101623
-
DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome
-
Ley TJ, Mardis ER, Ding L, Fulton B, McLellan MD, Chen K, et al. DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome. Nature. 2008;456:66-72.
-
(2008)
Nature.
, vol.456
, pp. 66-72
-
-
Ley, T.J.1
Mardis, E.R.2
Ding, L.3
Fulton, B.4
McLellan, M.D.5
Chen, K.6
-
17
-
-
79955016374
-
Identification of a novel TP53 cancer susceptibility mutation through whole-genome sequencing of a patient with therapy-related AML
-
Link DC, Schuettpelz LG, Shen D, Wang J, Walter MJ, Kulkarni S, et al. Identification of a novel TP53 cancer susceptibility mutation through whole-genome sequencing of a patient with therapy-related AML. JAMA. 2011;305:1568-76.
-
(2011)
JAMA.
, vol.305
, pp. 1568-1576
-
-
Link, D.C.1
Schuettpelz, L.G.2
Shen, D.3
Wang, J.4
Walter, M.J.5
Kulkarni, S.6
-
18
-
-
77951589703
-
Clinical assessment incorporating a personal genome
-
Ashley EA, Butte AJ, Wheeler MT, Chen R, Klein TE, Dewey FE, et al. Clinical assessment incorporating a personal genome. Lancet. 2010;375:1525-35.
-
(2010)
Lancet.
, vol.375
, pp. 1525-1535
-
-
Ashley, E.A.1
Butte, A.J.2
Wheeler, M.T.3
Chen, R.4
Klein, T.E.5
Dewey, F.E.6
-
19
-
-
80053447840
-
Phased whole-genome genetic risk in a family quartet using a major allele reference sequence
-
Dewey FE, Chen R, Cordero SP, Ormond KE, Caleshu C, Karczewski KJ, et al. Phased whole-genome genetic risk in a family quartet using a major allele reference sequence. PLoS Genet. 2011;7:e1002280.
-
(2011)
PLoS Genet.
, vol.7
, pp. e1002280
-
-
Dewey, F.E.1
Chen, R.2
Cordero, S.P.3
Ormond, K.E.4
Caleshu, C.5
Karczewski, K.J.6
-
20
-
-
84916634710
-
Molecular diagnosis of long QT syndrome at 10 days of life by rapid whole genome sequencing
-
Priest JR, Ceresnak SR, Dewey FE, Malloy-Walton LE, Dunn K, Grove ME, et al. Molecular diagnosis of long QT syndrome at 10 days of life by rapid whole genome sequencing. Heart Rhythm. 2014;11:1707-13.
-
(2014)
Heart Rhythm.
, vol.11
, pp. 1707-1713
-
-
Priest, J.R.1
Ceresnak, S.R.2
Dewey, F.E.3
Malloy-Walton, L.E.4
Dunn, K.5
Grove, M.E.6
-
21
-
-
84929026065
-
Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings
-
Willig LK, Petrikin JE, Smith LD, Saunders CJ, Thiffault I, Miller NA, et al. Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings. Lancet Respir Med. 2015;3:377-87.
-
(2015)
Lancet Respir Med.
, vol.3
, pp. 377-387
-
-
Willig, L.K.1
Petrikin, J.E.2
Smith, L.D.3
Saunders, C.J.4
Thiffault, I.5
Miller, N.A.6
-
22
-
-
84915803267
-
Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders
-
Soden SE, Saunders CJ, Willig LK, Farrow EG, Smith LD, Petrikin JE, et al. Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders. Sci Transl Med. 2014;6:265ra168.
-
(2014)
Sci Transl Med
, vol.6
-
-
Soden, S.E.1
Saunders, C.J.2
Willig, L.K.3
Farrow, E.G.4
Smith, L.D.5
Petrikin, J.E.6
-
23
-
-
84867214350
-
Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units
-
Saunders CJ, Miller NA, Soden SE, Dinwiddie DL, Noll A, Abu Alnadi N, et al. Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units. Sci Transl Med. 2012;4:154ra135.
-
(2012)
Sci Transl Med
, vol.4
-
-
Saunders, C.J.1
Miller, N.A.2
Soden, S.E.3
Dinwiddie, D.L.4
Noll, A.5
Abu Alnadi, N.6
-
24
-
-
84938066152
-
Emergency medical genomes: a breakthrough application of precision medicine
-
Kingsmore SF, Petrikin J, Willig LK, Guest E. Emergency medical genomes: a breakthrough application of precision medicine. Genome Med. 2015;7:82.
-
(2015)
Genome Med.
, vol.7
, pp. 82
-
-
Kingsmore, S.F.1
Petrikin, J.2
Willig, L.K.3
Guest, E.4
-
25
-
-
84923798102
-
An analytical framework for optimizing variant discovery from personal genomes
-
Highnam G, Wang JJ, Kusler D, Zook J, Vijayan V, Leibovich N, et al. An analytical framework for optimizing variant discovery from personal genomes. Nat Commun. 2015;6:6.
-
(2015)
Nat Commun.
, vol.6
, pp. 6
-
-
Highnam, G.1
Wang, J.J.2
Kusler, D.3
Zook, J.4
Vijayan, V.5
Leibovich, N.6
-
26
-
-
84897387657
-
Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls
-
Zook JM, Chapman B, Wang J, Mittelman D, Hofmann O, Hide W, et al. Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls. Nat Biotechnol. 2014;32:246-51.
-
(2014)
Nat Biotechnol.
, vol.32
, pp. 246-251
-
-
Zook, J.M.1
Chapman, B.2
Wang, J.3
Mittelman, D.4
Hofmann, O.5
Hide, W.6
-
27
-
-
84959335050
-
College of American pathologists' laboratory standards for next generation sequence clinical testing
-
Aziz N, Lynn B, Driscoll D, Gibson J, Grody W, Hegde M, et al. College of American pathologists' laboratory standards for next generation sequence clinical testing. J Mol Diagn. 2012;14:742.
-
(2012)
J Mol Diagn.
, vol.14
, pp. 742
-
-
Aziz, N.1
Lynn, B.2
Driscoll, D.3
Gibson, J.4
Grody, W.5
Hegde, M.6
-
28
-
-
84899475755
-
BAYSIC: a Bayesian method for combining sets of genome variants with improved specificity and sensitivity
-
Cantarel BL, Weaver D, McNeill N, Zhang JH, Mackey AJ, Reese J. BAYSIC: a Bayesian method for combining sets of genome variants with improved specificity and sensitivity. BMC Bioinformatics. 2014;15:104.
-
(2014)
BMC Bioinformatics.
, vol.15
, pp. 104
-
-
Cantarel, B.L.1
Weaver, D.2
McNeill, N.3
Zhang, J.H.4
Mackey, A.J.5
Reese, J.6
-
29
-
-
84901984971
-
Joint variant and de novo mutation identification on pedigrees from high-throughput sequencing data
-
Cleary JG, Braithwaite R, Gaastra K, Hilbush BS, Inglis S, Irvine SA, et al. Joint variant and de novo mutation identification on pedigrees from high-throughput sequencing data. J Comput Biol. 2014;21:405-19.
-
(2014)
J Comput Biol.
, vol.21
, pp. 405-419
-
-
Cleary, J.G.1
Braithwaite, R.2
Gaastra, K.3
Hilbush, B.S.4
Inglis, S.5
Irvine, S.A.6
-
30
-
-
84919650082
-
Whole genome sequencing (WGS), whole exome sequencing (WES) and clinical exome sequencing (CES) in patient care
-
Klein HG, Bauer P, Hambuch T. Whole genome sequencing (WGS), whole exome sequencing (WES) and clinical exome sequencing (CES) in patient care. LaboratoriumsMedizin-Journal of Laboratory Medicine. 2014;38:221-30.
-
(2014)
LaboratoriumsMedizin-Journal of Laboratory Medicine.
, vol.38
, pp. 221-230
-
-
Klein, H.G.1
Bauer, P.2
Hambuch, T.3
-
31
-
-
84897403748
-
Comparison of somatic mutation calling methods in amplicon and whole exome sequence data
-
Xu HL, DiCarlo J, Satya RV, Peng Q, Wang YX. Comparison of somatic mutation calling methods in amplicon and whole exome sequence data. BMC Genomics. 2014;15:244.
-
(2014)
BMC Genomics.
, vol.15
, pp. 244
-
-
Xu, H.L.1
DiCarlo, J.2
Satya, R.V.3
Peng, Q.4
Wang, Y.X.5
-
32
-
-
84900476010
-
Analytical validation of whole exome and whole genome sequencing for clinical applications
-
Linderman MD, Brandt T, Edelmann L, Jabado O, Kasai Y, Kornreich R, et al. Analytical validation of whole exome and whole genome sequencing for clinical applications. BMC Med Genomics. 2014;7:20.
-
(2014)
BMC Med Genomics.
, vol.7
, pp. 20
-
-
Linderman, M.D.1
Brandt, T.2
Edelmann, L.3
Jabado, O.4
Kasai, Y.5
Kornreich, R.6
-
33
-
-
84938894761
-
Achieving high-sensitivity for clinical applications using augmented exome sequencing
-
Patwardhan A, Harris J, Leng N, Bartha G, Church DM, Luo S, et al. Achieving high-sensitivity for clinical applications using augmented exome sequencing. Genome Med. 2015;7:71.
-
(2015)
Genome Med.
, vol.7
, pp. 71
-
-
Patwardhan, A.1
Harris, J.2
Leng, N.3
Bartha, G.4
Church, D.M.5
Luo, S.6
-
34
-
-
84890081976
-
Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM
-
arXiv:13033997 [q-bioGN]
-
Li H. Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM. arXiv:13033997 [q-bioGN] 2013.
-
(2013)
-
-
Li, H.1
-
35
-
-
79955483667
-
A framework for variation discovery and genotyping using next-generation DNA sequencing data
-
DePristo MA, Banks E, Poplin R, Garimella KV, Maguire JR, Hartl C, et al. A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nature Genetics. 2011;43:491-8.
-
(2011)
Nature Genetics.
, vol.43
, pp. 491-498
-
-
DePristo, M.A.1
Banks, E.2
Poplin, R.3
Garimella, K.V.4
Maguire, J.R.5
Hartl, C.6
-
36
-
-
84905576523
-
Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications
-
Rimmer A, Phan H, Mathieson I, Iqbal Z, Twigg SRF, Wilkie AOM, et al. Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications. Nat Genet. 2014;46:912-8.
-
(2014)
Nat Genet.
, vol.46
, pp. 912-918
-
-
Rimmer, A.1
Phan, H.2
Mathieson, I.3
Iqbal, Z.4
Twigg, S.R.F.5
Wilkie, A.O.M.6
-
37
-
-
84921783122
-
Accurate de novo and transmitted indel detection in exome-capture data using microassembly
-
Narzisi G, O'Rawe JA, Iossifov I, Fang H, Lee YH, Wang ZH, et al. Accurate de novo and transmitted indel detection in exome-capture data using microassembly. Nat Methods. 2014;11:1033-6.
-
(2014)
Nat Methods.
, vol.11
, pp. 1033-1036
-
-
Narzisi, G.1
O'Rawe, J.A.2
Iossifov, I.3
Fang, H.4
Lee, Y.H.5
Wang, Z.H.6
-
38
-
-
77956534324
-
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
-
Wang K, Li MY, Hakonarson H. ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. Nucleic Acids Res. 2010;38:e164.
-
(2010)
Nucleic Acids Res.
, vol.38
, pp. e164
-
-
Wang, K.1
Li, M.Y.2
Hakonarson, H.3
-
39
-
-
84880535720
-
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing
-
Green RC, Berg JS, Grody WW, Kalia SS, Korf BR, Martin CL, et al. ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. Genet Med. 2013;15:565-74.
-
(2013)
Genet Med.
, vol.15
, pp. 565-574
-
-
Green, R.C.1
Berg, J.S.2
Grody, W.W.3
Kalia, S.S.4
Korf, B.R.5
Martin, C.L.6
-
40
-
-
77951770756
-
BEDTools: a flexible suite of utilities for comparing genomic features
-
Quinlan AR, Hall IM. BEDTools: a flexible suite of utilities for comparing genomic features. Bioinformatics. 2010;26:841-2.
-
(2010)
Bioinformatics.
, vol.26
, pp. 841-842
-
-
Quinlan, A.R.1
Hall, I.M.2
-
41
-
-
84943587934
-
Good laboratory practice for clinical next-generation sequencing informatics pipelines
-
Gargis AS, Kalman L, Bick DP, da Silva C, Dimmock DP, Funke BH, et al. Good laboratory practice for clinical next-generation sequencing informatics pipelines. Nat Biotechnol. 2015;33:689-93.
-
(2015)
Nat Biotechnol.
, vol.33
, pp. 689-693
-
-
Gargis, A.S.1
Kalman, L.2
Bick, D.P.3
Silva, C.4
Dimmock, D.P.5
Funke, B.H.6
-
42
-
-
7244247384
-
Shotgun sequence assembly and recent segmental duplications within the human genome
-
She XW, Jiang ZX, Clark RL, Liu G, Cheng Z, Tuzun E, et al. Shotgun sequence assembly and recent segmental duplications within the human genome. Nature. 2004;431:927-30.
-
(2004)
Nature.
, vol.431
, pp. 927-930
-
-
She, X.W.1
Jiang, Z.X.2
Clark, R.L.3
Liu, G.4
Cheng, Z.5
Tuzun, E.6
-
43
-
-
84957823399
-
Analysis of protein-coding genetic variation in 60,706 humans
-
Lek M, Karczewski K, Minikel E, Samocha K, Banks E, Fennell T, et al. Analysis of protein-coding genetic variation in 60,706 humans. BioRxiv. 2015. doi: 10.1101/030338.
-
(2015)
BioRxiv
-
-
Lek, M.1
Karczewski, K.2
Minikel, E.3
Samocha, K.4
Banks, E.5
Fennell, T.6
-
44
-
-
78650909427
-
Limitations of next-generation genome sequence assembly
-
Alkan C, Sajjadian S, Eichler EE. Limitations of next-generation genome sequence assembly. Nat Methods. 2011;8:61-5.
-
(2011)
Nat Methods.
, vol.8
, pp. 61-65
-
-
Alkan, C.1
Sajjadian, S.2
Eichler, E.E.3
-
45
-
-
84925497196
-
Resolving the complexity of the human genome using single-molecule sequencing
-
Chaisson MJ, Huddleston J, Dennis MY, Sudmant PH, Malig M, Hormozdiari F, et al. Resolving the complexity of the human genome using single-molecule sequencing. Nature. 2015;517:608-11.
-
(2015)
Nature.
, vol.517
, pp. 608-611
-
-
Chaisson, M.J.1
Huddleston, J.2
Dennis, M.Y.3
Sudmant, P.H.4
Malig, M.5
Hormozdiari, F.6
-
46
-
-
84973543241
-
Comparing variant call files for performance benchmarking of next-generation sequencing variant calling pipelines
-
Cleary JG, Braithwaite R, Gaastra K, Hilbush BS, Inglis S, Irvine SA, et al. Comparing variant call files for performance benchmarking of next-generation sequencing variant calling pipelines. 2015. doi: 10.1101/023754.
-
(2015)
-
-
Cleary, J.G.1
Braithwaite, R.2
Gaastra, K.3
Hilbush, B.S.4
Inglis, S.5
Irvine, S.A.6
-
47
-
-
84946100079
-
The UCSC Genome Browser database: 2015 update
-
Rosenbloom KR, Armstrong J, Barber GP, Casper J, Clawson H, Diekhans M, et al. The UCSC Genome Browser database: 2015 update. Nucleic Acids Res. 2015;43(Database Issue):D670-81.
-
(2015)
Nucleic Acids Res
, vol.43
, Issue.DATABASE ISSUE
, pp. D670-D681
-
-
Rosenbloom, K.R.1
Armstrong, J.2
Barber, G.P.3
Casper, J.4
Clawson, H.5
Diekhans, M.6
-
48
-
-
84901410645
-
Choice of transcripts and software has a large effect on variant annotation
-
McCarthy DJ, Humburg P, Kanapin A, Rivas MA, Gaulton K, Cazier JB, et al. Choice of transcripts and software has a large effect on variant annotation. Genome Med. 2014;6:26.
-
(2014)
Genome Med.
, vol.6
, pp. 26
-
-
McCarthy, D.J.1
Humburg, P.2
Kanapin, A.3
Rivas, M.A.4
Gaulton, K.5
Cazier, J.B.6
-
49
-
-
77957738952
-
Alternative promoter usage and splicing of the human SCN5A gene contribute to transcript heterogeneity
-
van Stuijvenberg L, Yildirim C, Kok BG, van Veen TA, Varró A, Winckels SK, et al. Alternative promoter usage and splicing of the human SCN5A gene contribute to transcript heterogeneity. DNA Cell Biol. 2010;29:577-87.
-
(2010)
DNA Cell Biol.
, vol.29
, pp. 577-587
-
-
Stuijvenberg, L.1
Yildirim, C.2
Kok, B.G.3
Veen, T.A.4
Varró, A.5
Winckels, S.K.6
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