Results 121 to 130 of about 487,550 (165)

Complete genome sequence of <i>Leclercia adecarboxylata</i> strain TB492 isolated from flue-cured tobacco leaves. [PDF]

open access: yesMicrobiol Resour Announc
Liu C   +11 more
europepmc   +1 more source

Pylluminator: fast and scalable analysis of DNA methylation data in Python. [PDF]

open access: yesBioinform Adv
Fanchon E   +4 more
europepmc   +1 more source

Illumina, Inc.

Pharmacogenomics, 2005
Illumina, Inc., based in San Diego (CA, USA), is a genomics tool company that develops and markets integrated array-based systems and assays for a broad range of applications including genotyping, gene expression and epigenetics. Product offerings range from focused assay sets (up to 1,536 multiplexed assays) to whole-genome analysis (>100,000 assays ...
Frank J, Steemers, Kevin L, Gunderson
openaire   +2 more sources

Illumina

Anthropologie et Sociétés
Cet article se présente comme un exercice de réflexivité critique suivant un projet mené dans un quartier de la ville de Québec, le quartier Saint-Roch, et ayant pour moteur l’art et la création comme forme d’accompagnement pour les personnes vivant avec des problématiques de santé mentale au sein de la communauté. Le projet,
Saillant, Francine   +2 more
openaire   +2 more sources

Best Practices for Illumina Library Preparation

Current Protocols in Human Genetics, 2019
AbstractIn this unit, we describe a set of protocols and recommendations for Illumina library preparation. We review best practices in template quantitation methods; template fragmentation methodologies; solid‐phase reverse‐immobilization cleanup, including buffer exchange and size selection; end repair, A‐tailing, and adapter ligation; indexing ...
Iraad F, Bronner, Michael A, Quail
openaire   +2 more sources

ANALYSIS OF CONTEXT-DEPENDENT ERRORS FOR ILLUMINA SEQUENCING

Journal of Bioinformatics and Computational Biology, 2012
The new generation of short-read sequencing technologies requires reliable measures of data quality. Such measures are especially important for variant calling. However, in the particular case of SNP calling, a great number of false-positive SNPs may be obtained. One needs to distinguish putative SNPs from sequencing or other errors. We found that not
Irina I. Abnizova   +10 more
openaire   +2 more sources

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