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Sequencing (Nucleic acids)
LE WE PMID CA
Sequencing (Nucleic acids)5483Sequenzierung (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

2009  
1
Generations of sequencing technologies.
[18992322] Genomics 93(2): 105-11 (2009)
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
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
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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