Sequencing (Nucleic acids)

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Sequencing (Nucleic acids)

LE WE PMID CA

Sequencing (Nucleic acids)

5483

Sequenzierung (Kernsaeuren)

Bioinformatics

Chromatin

Exome capture

Genetics (GWAS Genome wide association study)

Genetics (Single nucleotid polymorphism)

Genomic and genetic analysis

Genomic capture

Microarray (Gene expression analysis)

Neoplasia (Personalized cancer therapy)

Neoplasia (Tumor biology and immunology)

Pyrosequencing

RNA (MicroRNA)

RNA (RNA Seq)

Sequencing (Nucleic acids)

Structure determination at molecular level and finer

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2008 2	Applications of next-generation sequencing technologies in functional genomics. [18703132] Genomics 92(5): 255-64 (2008)
2009 3	Next-generation DNA sequencing of paired-end tags (PET) for transcriptome and genome analyses. [19339662] Genome Res 19(4): 521-32 (2009)
2008 4	The new paradigm of flow cell sequencing. [18519653] Genome Res 18(6): 839-46 (2008)
2007 5	Multiple sequence alignment: in pursuit of homologous DNA positions. [17272647] Genome Res 17(2): 127-35 (2007)
2005 6	Genome annotation past, present, and future: how to define an ORF at each locus. [16339376] Genome Res 15(12): 1777-86 (2005)
2005 7	Emerging technologies in DNA sequencing. [16339375] Genome Res 15(12): 1767-76 (2005)
2001 8	Pyrosequencing sheds light on DNA sequencing. [11156611] Genome Res 11(1): 3-11 (2001)
2000 9	Automation for genomics, part two: sequencers, microarrays, and future trends. [10984447] Genome Res 10(9): 1288-303 (2000)
2000 10	Automation for genomics, part one: preparation for sequencing. [10958626] Genome Res 10(8): 1081-92 (2000)
2000 11	Powers and pitfalls in sequence analysis: the 70% hurdle. [10779480] Genome Res 10(4): 398-400 (2000)
1998 12	Base-calling of automated sequencer traces using phred. I. Accuracy assessment. [9521921] Genome Res 8(3): 175-85 (1998)
2010 13	An integrated system for DNA sequencing by synthesis using novel nucleotide analogues. [20121268] Acc Chem Res 43(4): 551-63 (2010)
2011 14	Base-calling for next-generation sequencing platforms. [21245079] Brief Bioinform 12(5): 489-97 (2011)
2010 15	A survey of sequence alignment algorithms for next-generation sequencing. [20460430] Brief Bioinform 11(5): 473-83 (2010)
2005 16	The many faces of sequence alignment. [15826353] Brief Bioinform 6(1): 6-22 (2005)
2010 17	A window into third-generation sequencing. [20858600] Hum Mol Genet 19(R2): R227-40 (2010)
2010 18	Exome sequencing: the sweet spot before whole genomes. [20705737] Hum Mol Genet 19(R2): R145-51 (2010)
2010 19	Massively parallel sequencing and rare disease. [20846941] Hum Mol Genet 19(R2): R119-24 (2010)
2009 20	Cancer genome sequencing: a review. [19808792] Hum Mol Genet 18(R2): R163-8 (2009)
2009 21	Current-generation high-throughput sequencing: deepening insights into mammalian transcriptomes. [19528315] Genes Dev 23(12): 1379-86 (2009)
2011 22	Genome-wide analysis of the relationships between DNaseI HS, histone modifications and gene expression reveals distinct modes of chromatin domains. [21685456] Nucleic Acids Res 39(17): 7428-43 (2011)
2011 23	Targeted next-generation sequencing: microdroplet PCR approach for variant detection in research and clinical samples. [21545251] Expert Rev Mol Diagn 11(4): 347-9 (2011)
2011 24	Genome diagnostics: next-generation sequencing, new genome-wide association studies and clinical challenges. [21902524] Expert Rev Mol Diagn 11(7): 663-6 (2011)
2010 25	Great expectations: using massively parallel sequencing to solve inherited disorders. [20964599] Expert Rev Mol Diagn 10(7): 833-6 (2010)
2010 26	Applications of nucleic acids technologies in molecular diagnostics; multiplex assays in real time format. [20964604] Expert Rev Mol Diagn 10(7): 853-5 (2010)
2008 27	Identification of microRNAs and other small regulatory RNAs using cDNA library sequencing. [18158127] Methods 44(1): 3-12 (2008)
2003 28	Alignment-free sequence comparison-a review. [12611807] Bioinformatics 19(4): 513-23 (2003)
2010 29	Next-generation sequencing and epigenome technologies: potential medical applications. [21050081] Expert Rev Med Devices 7(6): 723-6 (2010)
2011 30	SOLiDzipper: A High Speed Encoding Method for the Next-Generation Sequencing Data. [21487532] Evol Bioinform Online 7(-): 1-6 (2011)
2011 31	The effect of next-generation sequencing technology on complex trait research. [21155765] Eur J Clin Invest 41(5): 561-7 (2011)
2011 32	The impact of next-generation sequencing on genomics. [21477781] J Genet Genomics 38(3): 95-109 (2011)
2010 33	Detecting structural variations in the human genome using next generation sequencing. [21216738] Brief Funct Genomics 9(5-6): 405-15 (2010)
2010 34	Recognition tunneling. [20522930] Nanotechnology 21(26): 262001 (2010)
2010 35	Assembly algorithms for next-generation sequencing data. [20211242] Genomics 95(6): 315-27 (2010)
2011 36	Sequencing technologies and genome sequencing. [21698376] J Appl Genet 52(4): 413-35 (2011)
2011 37	RNA sequencing: advances, challenges and opportunities. [21191423] Nat Rev Genet 12(2): 87-98 (2011)
2009 38	RNA-Seq: a revolutionary tool for transcriptomics. [19015660] Nat Rev Genet 10(1): 57-63 (2009)
2010 39	Next-generation sequencing techniques for eukaryotic microorganisms: sequencing-based solutions to biological problems. [20601439] Eukaryot Cell 9(9): 1300-10 (2010)
2011 40	The bioinformatics of next generation sequencing: a meeting report. [20823082] J Mol Cell Biol 3(3): 147-50 (2011)
2011 41	Future medical applications of single-cell sequencing in cancer. [21631906] Genome Med 3(5): 31 (2011)
2010 42	Assembly of large genomes using second-generation sequencing. [20508146] Genome Res 20(9): 1165-73 (2010)
2010 43	Accurate detection and genotyping of SNPs utilizing population sequencing data. [20150320] Genome Res 20(4): 537-45 (2010)
2002 44	Discovery of single nucleotide polymorphisms and mutations by pyrosequencing. [18628881] Comp Funct Genomics 3(1): 51-6 (2002)
2010 45	Next generation sequencing for clinical diagnostics-principles and application to targeted resequencing for hypertrophic cardiomyopathy: a paper from the 2009 William Beaumont Hospital Symposium on Molecular Pathology. [20805560] J Mol Diagn 12(5): 539-51 (2010)
2008 46	Keeping up with the next generation: massively parallel sequencing in clinical diagnostics. [18832462] J Mol Diagn 10(6): 484-92 (2008)
2011 47	Microarrays, deep sequencing and the true measure of the transcriptome. [21627854] BMC Biol 9(-): 34 (2011)
2011 48	Multiple platform assessment of the EGF dependent transcriptome by microarray and deep tag sequencing analysis. [21699700] BMC Genomics 12(-): 326 (2011)
2009 49	DNA sequencing by CE. [19517496] Electrophoresis 30 Suppl 1(-): S196-202 (2009)
2011 50	On optimal pooling designs to identify rare variants through massive resequencing. [21254222] Genet Epidemiol 35(3): 139-47 (2011)
2011 51	Introduction to bioinformatics: sequencing technology. [22053303] Asia Pac Allergy 1(2): 93-7 (2011)
2009 52	Next is now: new technologies for sequencing of genomes, transcriptomes, and beyond. [19157957] Curr Opin Plant Biol 12(2): 107-18 (2009)
2011 53	Single-molecule direct RNA sequencing without cDNA synthesis. [21957044] Wiley Interdiscip Rev RNA 2(4): 565-70 (2011)
2010 54	Next generation sequencing based approaches to epigenomics. [21266347] Brief Funct Genomics 9(5-6): 455-65 (2010)
2010 55	Overcoming bias and systematic errors in next generation sequencing data. [21144010] Genome Med 2(12): 87 (2010)
2011 56	Applications of next generation sequencing in molecular ecology of non-model organisms. [21139633] Heredity (Edinb) 107(1): 1-15 (2011)

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