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Institution

Applied Biosystems

About: Applied Biosystems is a based out in . It is known for research contribution in the topics: Mass spectrometry & Capillary electrophoresis. The organization has 1521 authors who have published 1579 publications receiving 285423 citations.


Papers
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Journal ArticleDOI
TL;DR: Oligodeoxynucleotides 18-150 bases in length were synthesized with both 0-(2-cyanoethyl)- and 0-(methyl)-phosphoramidites as mentioned in this paper.
Abstract: Oligodeoxynucleotides 18–150 bases in length were synthesized with both 0-(2-cyanoethyl)- and 0-(methyl)-phosphoramidites. After enzymatic degradation of the purified products, base modification and composition were evaluated by HPLC. Additionally, synthesis of 5′-d[GCGCGCTT] with O-(methyl) phosphorus protection generated 3-methylthymidine when thiophenoxide was omitted from the deprotection protocol.

20 citations

Journal ArticleDOI
TL;DR: It appears that the combination of electroblotting and microbore LC represents a powerful approach for microsample preparation, and the Aebersold et al. procedure was substantially modified and improved.

20 citations

Patent
30 Jun 2004
TL;DR: In this paper, the methods for detecting an RNA such as a small RNA comprising up to about 40 nucleotides are disclosed, which comprise forming a ligation mixture comprising a sample suspected of comprising the small RNA, a ligase and a target probe set.
Abstract: Methods for detecting an RNA such as a small RNA comprising up to about 40 nucleotides are disclosed. The methods comprise forming a ligation mixture comprising a sample suspected of comprising the small RNA, a ligase and a target probe set. The target probe set comprises a first target probe comprising a 3′ portion that hybridizes to the small RNA and a 5′ portion having a first PCR primer target sequence, and a second target probe comprising a 5′ portion that hybridizes to the RNA immediately adjacent to the 3′ end of the first target probe and a 3′ portion having a second PCR primer target sequence. The target probe set hybridizes to the RNA and ligates to form a probe set ligation sequence. A probe set ligation sequence can be amplified and detected using a polymerase chain reaction.

20 citations

Book ChapterDOI
TL;DR: The typical workflows for the selection of markers for association studies utilizing the SNPbrowser software is reviewed, a freely available, stand-alone application that incorporates the HapMap database together with gene and SNP annotations.
Abstract: The design of genetic association studies using single-nucleotide polymorphisms (SNPs) requires the selection of subsets of the variants providing high statistical power at a reasonable cost. SNPs must be selected to maximize the probability that a causative mutation is in linkage disequilibrium (LD) with at least one marker genotyped in the study. The HapMap Project performed a genome-wide survey of genetic variation with over 3 million SNPs typed in four populations, providing a rich resource to inform the design of association studies. A number of strategies have been proposed for the selection of SNPs based on observed LD, including construction of metric LD maps and the selection of haplotype-tagging SNPs. Power calculations are important at the study design stage to ensure successful results. Integrating these methods and annotations can be challenging: the algorithms required to implement these methods are complex to deploy, and all the necessary data and annotations are deposited in disparate databases. Here, we review the typical workflows for the selection of markers for association studies utilizing the SNPbrowser software, a freely available, stand-alone application that incorporates the HapMap database together with gene and SNP annotations. Selected SNPs are screened for their conversion potential to genotyping platforms, expediting the set up of genetic studies with an increased probability of success.

20 citations

Journal ArticleDOI
H.E. Schwartz1
TL;DR: In this paper, the authors compare the results of chromatographie fluide supercritique (SFC) and thermogravimetrique sous vide on a colonne a garnissage contient de la silice and du siloxane polymere.
Abstract: Etude de la rapidite, de la precision et de la reproductibilite de la methode qui consiste a simuler une distillation par chromatographie fluide supercritique (SFC). La colonne a garnissage utilisee contient de la silice et du siloxane polymere. L'etude est realisee sur du petrole brut provenant de Maljamar (Nouveau Mexique). Les resultats sont compares a ceux obtenus par chromatographie SFC sur colonne capillaire et par analyse thermogravimetrique sous vide. Les trois methodes donnent des resultats comparables

20 citations


Authors

Showing all 1521 results

NameH-indexPapersCitations
Richard A. Gibbs172889249708
Friedrich C. Luft113109547619
Alexander N. Glazer7120821068
Vineet Bafna6823642574
Kevin R. Coombes6330823592
Darryl J. Pappin6117029409
Mark D. Johnson6028916103
György Marko-Varga5640912600
Paul Thomas5612844810
Gerald Zon5525611126
Michael W. Hunkapiller5113029756
Bjarni V. Halldorsson5114513180
David H. Hawke501579824
Ellson Y. Chen507128836
Sridhar Hannenhalli4916221959
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20182
20171
20164
20152
20147
201313