ריצוף אקסום (Hebrew Wikipedia)

Analysis of information sources in references of the Wikipedia article "ריצוף אקסום" in Hebrew language version.

refsWebsite

Global rank Hebrew rank

17nih.gov

4^th place

18^th place

11doi.org

2^nd place

10^th place

3harvard.edu

18^th place

109^th place

1worldcat.org

5^th place

31^st place

1le.ac.uk

5,357^th place

2,461^st place

doi.org

Ng SB, Turner EH, Robertson PD, Flygare SD, Bigham AW, Lee C, Shaffer T, Wong M, Bhattacharjee A, Eichler EE, Bamshad M, Nickerson DA, Shendure J (10 בספטמבר 2009). "Targeted capture and massively parallel sequencing of 12 human exomes". Nature. 461 (7261): 272–276. Bibcode:2009Natur.461..272N. doi:10.1038/nature08250. PMC 2844771. PMID 19684571. {{cite journal}}: (עזרה)
Sarah B Ng; Kati J Buckingham; Choli Lee; Abigail W Bigham; Holly K Tabor; Karin M Dent; Chad D Huff; Paul T Shannon; Ethylin Wang Jabs; Deborah A Nickerson; Jay Shendure (2010). "Exome sequencing identifies the cause of a mendelian disorder". Nature Genetics. 42 (1): 30–35. doi:10.1038/ng.499. PMC 2847889. PMID 19915526.
Wang, D. G.; Fan, J. B.; Siao, C. J.; Berno, A.; Young, P.; Sapolsky, R.; Ghandour, G.; Perkins, N.; Winchester, E. (1998-05-15). "Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome". Science. 280 (5366): 1077–1082. Bibcode:1998Sci...280.1077W. doi:10.1126/science.280.5366.1077. ISSN 0036-8075. PMID 9582121.
Rauch, A; Hoyer, J; Guth, S; Zweier, C; Kraus, C; Becker, C; Zenker, M; Hüffmeier, U; Thiel, C; Rüschendorf, F; Nürnberg, P (1 אוק' 2006). "Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation". American Journal of Medical Genetics Part A. 140 (19): 2063–74. doi:10.1002/ajmg.a.31416. PMID 16917849. {{cite journal}}: (עזרה)
Stavros Basiardes; Rose Veile; Cindy Helms; Elaine R. Mardis; Anne M. Bowcock; Michael Lovett (2005). "Direct Genomic Selection". Nature Methods. 1 (2): 63–69. doi:10.1038/nmeth0105-63. PMID 16152676.
Teer, J. K.; Mullikin, J. C. (12 באוגוסט 2010). "Exome sequencing: the sweet spot before whole genomes". Human Molecular Genetics. 19 (R2): R145–R151. doi:10.1093/hmg/ddq333. PMC 2953745. PMID 20705737. {{cite journal}}: (עזרה)
Emily H. Turner; Sarah B. Ng; Deborah A. Nickerson; Jay Shendure (2009). "Methods for Genomic Partitioning". Annu Rev Genom Hum Genet. 10 (1): 30–35. doi:10.1146/annurev-genom-082908-150112. PMID 19630561.
Mertes F, Elsharawy A, Sauer S, van Helvoort JM, van der Zaag PJ, Franke A, Nilsson M, Lehrach H, Brookes AJ (2011). "Targeted enrichment of genomic DNA regions for next-generation sequencing" (PDF). Brief. Funct. Genomics. 10 (6): 374–386. doi:10.1093/bfgp/elr033. PMC 3245553. PMID 22121152.
Choi M, Scholl UI, Ji W, Liu T, Tikhonova IR, Zumbo P, Nayir A, Bakkaloğlu A, Ozen S, Sanjad S, Nelson-Williams C, Farhi A, Mane S, Lifton RP (10 בנובמבר 2009). "Genetic diagnosis by whole exome capture and massively parallel DNA sequencing". Proc Natl Acad Sci U S A. 106 (45): 19096–19101. Bibcode:2009PNAS..10619096C. doi:10.1073/pnas.0910672106. PMC 2768590. PMID 19861545. {{cite journal}}: (עזרה)
Kahvejian A, Quackenbush J, Thompson JF (2008). "What would you do if you could sequence everything?". Nature Biotechnology. 26 (10): 1125–1133. doi:10.1038/nbt1494. PMC 4153598. PMID 18846086.
Lira Mamanova; Coffey, Alison J; Scott, Carol E; Kozarewa, Iwanka; Turner, Emily H; Kumar, Akash; Howard, Eleanor; Shendure, Jay; Turner, Daniel J; et al. (בפברואר 2010). "Target-enrichment strategies for nextgeneration sequencing". Nature Methods. 7 (2): 111–118. doi:10.1038/nmeth.1419. PMID 20111037. {{cite journal}}: (עזרה)

harvard.edu

ui.adsabs.harvard.edu

Ng SB, Turner EH, Robertson PD, Flygare SD, Bigham AW, Lee C, Shaffer T, Wong M, Bhattacharjee A, Eichler EE, Bamshad M, Nickerson DA, Shendure J (10 בספטמבר 2009). "Targeted capture and massively parallel sequencing of 12 human exomes". Nature. 461 (7261): 272–276. Bibcode:2009Natur.461..272N. doi:10.1038/nature08250. PMC 2844771. PMID 19684571. {{cite journal}}: (עזרה)
Wang, D. G.; Fan, J. B.; Siao, C. J.; Berno, A.; Young, P.; Sapolsky, R.; Ghandour, G.; Perkins, N.; Winchester, E. (1998-05-15). "Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome". Science. 280 (5366): 1077–1082. Bibcode:1998Sci...280.1077W. doi:10.1126/science.280.5366.1077. ISSN 0036-8075. PMID 9582121.
Choi M, Scholl UI, Ji W, Liu T, Tikhonova IR, Zumbo P, Nayir A, Bakkaloğlu A, Ozen S, Sanjad S, Nelson-Williams C, Farhi A, Mane S, Lifton RP (10 בנובמבר 2009). "Genetic diagnosis by whole exome capture and massively parallel DNA sequencing". Proc Natl Acad Sci U S A. 106 (45): 19096–19101. Bibcode:2009PNAS..10619096C. doi:10.1073/pnas.0910672106. PMC 2768590. PMID 19861545. {{cite journal}}: (עזרה)

le.ac.uk

lra.le.ac.uk

Mertes F, Elsharawy A, Sauer S, van Helvoort JM, van der Zaag PJ, Franke A, Nilsson M, Lehrach H, Brookes AJ (2011). "Targeted enrichment of genomic DNA regions for next-generation sequencing" (PDF). Brief. Funct. Genomics. 10 (6): 374–386. doi:10.1093/bfgp/elr033. PMC 3245553. PMID 22121152.

nih.gov

pubmed.ncbi.nlm.nih.gov

Ng SB, Turner EH, Robertson PD, Flygare SD, Bigham AW, Lee C, Shaffer T, Wong M, Bhattacharjee A, Eichler EE, Bamshad M, Nickerson DA, Shendure J (10 בספטמבר 2009). "Targeted capture and massively parallel sequencing of 12 human exomes". Nature. 461 (7261): 272–276. Bibcode:2009Natur.461..272N. doi:10.1038/nature08250. PMC 2844771. PMID 19684571. {{cite journal}}: (עזרה)
Sarah B Ng; Kati J Buckingham; Choli Lee; Abigail W Bigham; Holly K Tabor; Karin M Dent; Chad D Huff; Paul T Shannon; Ethylin Wang Jabs; Deborah A Nickerson; Jay Shendure (2010). "Exome sequencing identifies the cause of a mendelian disorder". Nature Genetics. 42 (1): 30–35. doi:10.1038/ng.499. PMC 2847889. PMID 19915526.
Wang, D. G.; Fan, J. B.; Siao, C. J.; Berno, A.; Young, P.; Sapolsky, R.; Ghandour, G.; Perkins, N.; Winchester, E. (1998-05-15). "Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome". Science. 280 (5366): 1077–1082. Bibcode:1998Sci...280.1077W. doi:10.1126/science.280.5366.1077. ISSN 0036-8075. PMID 9582121.
Rauch, A; Hoyer, J; Guth, S; Zweier, C; Kraus, C; Becker, C; Zenker, M; Hüffmeier, U; Thiel, C; Rüschendorf, F; Nürnberg, P (1 אוק' 2006). "Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation". American Journal of Medical Genetics Part A. 140 (19): 2063–74. doi:10.1002/ajmg.a.31416. PMID 16917849. {{cite journal}}: (עזרה)
Stavros Basiardes; Rose Veile; Cindy Helms; Elaine R. Mardis; Anne M. Bowcock; Michael Lovett (2005). "Direct Genomic Selection". Nature Methods. 1 (2): 63–69. doi:10.1038/nmeth0105-63. PMID 16152676.
Teer, J. K.; Mullikin, J. C. (12 באוגוסט 2010). "Exome sequencing: the sweet spot before whole genomes". Human Molecular Genetics. 19 (R2): R145–R151. doi:10.1093/hmg/ddq333. PMC 2953745. PMID 20705737. {{cite journal}}: (עזרה)
Emily H. Turner; Sarah B. Ng; Deborah A. Nickerson; Jay Shendure (2009). "Methods for Genomic Partitioning". Annu Rev Genom Hum Genet. 10 (1): 30–35. doi:10.1146/annurev-genom-082908-150112. PMID 19630561.
Mertes F, Elsharawy A, Sauer S, van Helvoort JM, van der Zaag PJ, Franke A, Nilsson M, Lehrach H, Brookes AJ (2011). "Targeted enrichment of genomic DNA regions for next-generation sequencing" (PDF). Brief. Funct. Genomics. 10 (6): 374–386. doi:10.1093/bfgp/elr033. PMC 3245553. PMID 22121152.
Choi M, Scholl UI, Ji W, Liu T, Tikhonova IR, Zumbo P, Nayir A, Bakkaloğlu A, Ozen S, Sanjad S, Nelson-Williams C, Farhi A, Mane S, Lifton RP (10 בנובמבר 2009). "Genetic diagnosis by whole exome capture and massively parallel DNA sequencing". Proc Natl Acad Sci U S A. 106 (45): 19096–19101. Bibcode:2009PNAS..10619096C. doi:10.1073/pnas.0910672106. PMC 2768590. PMID 19861545. {{cite journal}}: (עזרה)
Kahvejian A, Quackenbush J, Thompson JF (2008). "What would you do if you could sequence everything?". Nature Biotechnology. 26 (10): 1125–1133. doi:10.1038/nbt1494. PMC 4153598. PMID 18846086.
Lira Mamanova; Coffey, Alison J; Scott, Carol E; Kozarewa, Iwanka; Turner, Emily H; Kumar, Akash; Howard, Eleanor; Shendure, Jay; Turner, Daniel J; et al. (בפברואר 2010). "Target-enrichment strategies for nextgeneration sequencing". Nature Methods. 7 (2): 111–118. doi:10.1038/nmeth.1419. PMID 20111037. {{cite journal}}: (עזרה)

ncbi.nlm.nih.gov

Ng SB, Turner EH, Robertson PD, Flygare SD, Bigham AW, Lee C, Shaffer T, Wong M, Bhattacharjee A, Eichler EE, Bamshad M, Nickerson DA, Shendure J (10 בספטמבר 2009). "Targeted capture and massively parallel sequencing of 12 human exomes". Nature. 461 (7261): 272–276. Bibcode:2009Natur.461..272N. doi:10.1038/nature08250. PMC 2844771. PMID 19684571. {{cite journal}}: (עזרה)
Sarah B Ng; Kati J Buckingham; Choli Lee; Abigail W Bigham; Holly K Tabor; Karin M Dent; Chad D Huff; Paul T Shannon; Ethylin Wang Jabs; Deborah A Nickerson; Jay Shendure (2010). "Exome sequencing identifies the cause of a mendelian disorder". Nature Genetics. 42 (1): 30–35. doi:10.1038/ng.499. PMC 2847889. PMID 19915526.
Teer, J. K.; Mullikin, J. C. (12 באוגוסט 2010). "Exome sequencing: the sweet spot before whole genomes". Human Molecular Genetics. 19 (R2): R145–R151. doi:10.1093/hmg/ddq333. PMC 2953745. PMID 20705737. {{cite journal}}: (עזרה)
Mertes F, Elsharawy A, Sauer S, van Helvoort JM, van der Zaag PJ, Franke A, Nilsson M, Lehrach H, Brookes AJ (2011). "Targeted enrichment of genomic DNA regions for next-generation sequencing" (PDF). Brief. Funct. Genomics. 10 (6): 374–386. doi:10.1093/bfgp/elr033. PMC 3245553. PMID 22121152.
Choi M, Scholl UI, Ji W, Liu T, Tikhonova IR, Zumbo P, Nayir A, Bakkaloğlu A, Ozen S, Sanjad S, Nelson-Williams C, Farhi A, Mane S, Lifton RP (10 בנובמבר 2009). "Genetic diagnosis by whole exome capture and massively parallel DNA sequencing". Proc Natl Acad Sci U S A. 106 (45): 19096–19101. Bibcode:2009PNAS..10619096C. doi:10.1073/pnas.0910672106. PMC 2768590. PMID 19861545. {{cite journal}}: (עזרה)
Kahvejian A, Quackenbush J, Thompson JF (2008). "What would you do if you could sequence everything?". Nature Biotechnology. 26 (10): 1125–1133. doi:10.1038/nbt1494. PMC 4153598. PMID 18846086.

worldcat.org

Wang, D. G.; Fan, J. B.; Siao, C. J.; Berno, A.; Young, P.; Sapolsky, R.; Ghandour, G.; Perkins, N.; Winchester, E. (1998-05-15). "Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome". Science. 280 (5366): 1077–1082. Bibcode:1998Sci...280.1077W. doi:10.1126/science.280.5366.1077. ISSN 0036-8075. PMID 9582121.